Herba Cistanche (Rou Cong-Rong): One Of The Best Pharmaceutical Gifts Of Traditional Chinese Medicine

Feb 23, 2023

Herba Cistanche (Rou Cong-Rong): One of the Best Pharmaceutical Gifts of Traditional Chinese Medicine 

Cistanche species, known as Rou Cong-Rong in Chinese, are an endangered wild species and are mainly distributed in the arid lands and warm deserts of northwestern China. Within Traditional Chinese Medicine (TCM), Herba Cistanche is applied as a tonic and/or in a formula for chronic renal disease, impotence, female infertility, morbid leucorrhea, profuse metrorrhagia, and senile constipation. The chemical constituents of Herba Cistanche mainly consist of volatile oils, nonvolatile phenylethanoid glycosides (PhGs), iridoids, lignans, alditols, oligosaccharides, and polysaccharides. There have been an increasing number of studies focusing on its bio-activities, including antioxidation, neuroprotection, and antiaging. The objective of this review is to introduce this herb to the world. Its taxonomy, distribution, and corresponding biological functions and molecular mechanisms are addressed in this review

Cistanche Hoffmg. Et Link is a genus within the Orobanchaceae family and includes 22 species throughout the world. The distance species include the perennial parasite herbs, which commonly attach to the roots of sand-fixing plants, such as Haloxylon ammo dendron, H. persicum, Kalidium foliated, and Tamarix plants (Li et al., 2013b). Generally, distance species distribute in arid lands and deserts in the northern hemisphere, such as the provinces of Xinjiang, Inner Mongolia, Gansu, Qinghai, and the Ningxia Autonomous Region in China in addition to similar regions of countries such as Iran, India, and Mongolia (Jiang and Tu, 2009). The growth and cultivation of cistanche species require severe environmental conditions: extreme arid climate, depauperate soils, large temperature differences, intensive sunshine, and less than 250 mm of annual precipitation (Qiao et al., 2007). 

Cistanche

Click cistanche tubulosa extract food grade supplement product


Among the 22 species in the world, six are found in China according to the Taxonomical Index of Chinese Higher Plants (Plant Institute of Chinese Academy of Science, 1994); however, a follow-up study indicated that only 4 species and 1 variation of cistanche exist in China, including Cistanche deserticola Y. C. Ma, C. tubulosa (Schenk) R. Wight, C. salsa (C. A. Mey.) G. Beck, C. salsa var. albiflflora P. F. Tu et Z. C. Lou and C. sinensis G. Beck (Jiang and Tu, 2009).

The Herba Cistanche (Rou Cong-Rong in Chinese) was first recorded in Shen Nong’s Chinese Materia Medica, referred to as the dried succulent stems of the cistanche species (Karalliedde and Kappagoda, 2009). Among all the tonics in traditional Chinese medicine (TCM), Herba Cistanche is widely accepted as a superior one and has even been given the name “Ginseng of the deserts.

” In TCM, Herba Cistanche is frequently prescribed to treat chronic renal disease, impotence, female infertility, morbid leucorrhea, profuse metrorrhagia, and senile constipation (Zhang et al., 2005). In 2000 and 2005, respectively, C. tubulosa, and C. deserticola were indexed in the Chinese Pharmacopeia (Pharmacopoeia, 2000)

 (Figure 1). C. tubulosa is offered as an alternative to C. deserticola because of its similar chemical constituents and pharmacological activities and its abundance (Pharmacopoeia, 2005). Other species of this genus, e.g., C. salsa and C. sinensis, are also used as alternatives in some areas. Cistanche is considered a newly cultivated plant in several regions in northwestern China, where the rainfall is low and soil desertification is severe. 

Since the 1980s, researchers have been interested in Herba Cistanche. A chemical analysis of Herba Cistanche revealed that essential oils, phenylethanoid glycosides (PhGs), iridoids, lignans, alditols, oligosaccharides, cistanosides, and polysaccharides were the main constituents (Jin and Zhang, 1994). Herba Cistanche extracts are pharmacologically active, with a range of functions that include improving chronic renal disease and senile constipation, increasing learning/memorizing ability, treating Alzheimer’s disease (AD), and improving immunity (Snytnikova et al., 2012; Zhang et al., 2012; Guo et al., 2013; Li et al., 2013a; Nan et al., 2013).

 Most pharmaceutical companies are hoping to find the next ‘miracle’ drug, such as artemisinin (qinghaosu), an antimalarial drug that is extracted from the medicinal plant sweet wormwood and has saved millions of lives. The other classic example of modern medicine that originated in TCM is arsenic trioxide, which was approved by the US Food and Drug Administration (FDA) to treat leukemia in 2000. The present overview focuses on the progress of the study of the chemical constituents of Herba Cistanche and some of its relevant pharmacological activities.


cistanche

CHEMICAL CONSTITUENTS Volatile Compounds

In essential oil of the Herba Cistanche, alkanes, alcohols, aldehydes, and heterocyclics were detected, and palmitic acid, linoleic acid, 14-methylpentadecanoate, ethyl palmitate, and 2,5,6-trimethylolethane were identifified. The total oils of C. tubulosa mainly consist of palmitic acid and linoleic acid, while the essential oil of C. salsa includes alkanes, alcohols, aldehydes, and some heterocyclic compounds (Jiang and Tu, 2009). The volatile compounds of Herba Cistanche, like essential oils, commonly can be extracted by steam distillation or lipophilic organic solvent. By extracting C. deserticola with petroleum ether and then analyzing the sample on a GC-MS, 25 volatile compounds were identified, and the 3 richest constituents in the petroleum ether extract are methyl 14-methylpentadecanoate (13.61%), ethyl palmitate (12.39%), and 2,5,6-trimethyl octane (7.60%) (Jiang and Tu, 2009). 

Non-Volatile Compounds

Among the non-volatile compounds of Herba Cistanche, more than 100 have currently been isolated and identifified. These compounds are mostly PhDs, iridoids, lignans, alditols, oligosaccharides, and polysaccharides. As an important class of the compounds that constitute Herba Cistanche, PhGs have been well studied (Table 1). To date, 34 PhG compounds have been successfully isolated from Herba Cistanche, including 22 disaccharide glycosides, 10 trisaccharide glycosides, and 2 monosaccharide glycosides. The empirical structural features of PhGs are as follows. 

(1) For disaccharide glycosides, the sugar moiety consists of glucose and rhamnose connected by a Glc (3 1) Rha linkage; the glucose commonly links directly to an aglycone, and a coumaroyl or caffeoyl is usually located at the C4 or C6 position. (2) For trisaccharide glycosides, there is another glucose or rhamnose at the C6 position of the inside glucose. Recently, Li et al. (2015) completed the first deep transcriptome sequencing of the flfleshy stem of C. deserticola by RNA-seq and identifified some key enzyme genes and pathways that are involved in the biosynthesis of lignin and PhGs, which provides valuable information for this medical plant. For the other non-volatile compounds of Herba Cistanche, 3 iridoid aglycones, and 14 iridoid glycosides have currently been isolated from cistanche species (Xie et al., 2006); 1 and 5 lignan glycosides have been isolated from C. deserticola and C. tubulosa, respectively. Only 2 alkaloids, betaine, and N, N-dimethyl glycine methyl ester, have been isolated from Herba Cistanche (Jiang and Tu, 2009). Small amounts of other compounds, such as phenolic glycosides, sterols or their glycosides, fatty acids, amino acids, and trace elements, are also present in Herba Cistanche (Snytnikovaet al., 2012). 

cistanche

PHARMACOLOGICAL ACTIVITIES 

Based on the neuroprotection, immune-enhancement, and sexual health properties of Herba Cistanche, we discussed this in the paper (Supplementary Figure S1).

Improvement of Brain Function

When considering learning and memory, three levels of mechanisms are involved: (1) the ability to acquire memory, i.e., learning ability; (2) the ability to store memory, i.e., consolidation; and (3) the ability to recall memorized information (Choi et al., 2011). The C. tubulosa extract was confirmed to significantly improve these mechanisms by preventing brain neuron apoptosis through the expression of apoptosis-related factors and neurotrophic factors in MES23.5 cells (Lin et al., 2013). C. tubulosa extracts, containing rich echinacoside, and octreotide, can alleviate the cognitive dysfunction caused by Aβ 142 by blocking amyloid deposition, reversing cholinergic, and hippocampal dopaminergic neuronal function in AD-like rat models (Wu et al., 2014). One of the PhGs, echinacoside, is typically known as the main phenolic component in the roots of Echinacea Angustifolia, which is widely used in Europe and North America for its immunoregulation properties. 

A recent study determined that echinacoside can rescue human fibroblasts (SHSY5Y) from TNFα-induced apoptosis. The results indicated that echinacoside protects the damaged fibroblasts by regulating the reactive oxygen species level in fibroblasts and the activation of caspase-3 (Zhao et al., 2010). In vitro and in vivo experiments have confirmed that individual PhGs can inhibit the apoptosis of neuronal cells induced by various chemicals (Tian and Pu, 2005; Geng et al., 2007). Therefore, the individual PhGs could be attractive candidates against some typical neurodegenerative disorders, such as dementia or Parkinson’s disease (PD). Moreover, an open-label, non-placebo-controlled study on C. tubulosa glycoside capsules (Memoregain R ) demonstrates that the drug has the potential to be a possible treatment option for mild to moderate AD, and all adverse reactions were mild. (Guo et al., 2013).

Similarly, the C. salsa extract can accelerate the proliferation of fibroblasts and promote the production of neurons by accelerating the growth of the neurites. It also has some properties as follows: prevents damage caused by cerebral ischemia-reperfusion; protects against apoptosis of the CA1 region of the hippocampus (Wang et al., 2004); and increases the number of neurotransmitters, such as dopamine (DA), noradrenaline (NA), and serotonin (5-HT), in the rat brain (Chen et al.,2007; Choi et al., 2011; Zhong et al., 2012). The nucleoside-rich fraction of C. salsa extract can inhibit reactive oxygen species, prevent DNA damage, enhance superoxide dismutase (SOD) activity, and prevent lipid peroxidation (Lin et al., 2002; Deng et al., 2004b; He et al., 2009a). Because acetonide has an extremely strong antioxidative effect that is 15 times stronger than resveratrol and five times stronger than vitamin C (Chiou et al., 2004). 

cistanche

Aphrodisiac Effect 

A recent study has demonstrated that an ethanol extract of C. tubulosa could increase the sex hormone levels by inducing testicular steroidogenic enzymes (e.g., CYP11A1, CYP17A1, CYP3A4) (Wang et al., 2015). Besides, the gene expression of 3β-hydroxysteroid dehydrogenase (3β-HSD), which is responsible for the synthesis of testosterone, 5α-reductase-2 and aldo-keto reductase (enzymes that are responsible for the synthesis of dihydrotestosterone), can be induced by the C. tubulosa extract, suggesting the positive effect of C. tubulosa extract on male hormone production (Shimoda et al., 2009). The acteoside, which was distilled from C. tubulosa, significantly shortened the latent period of penis erection (p < 0.01), increased the number of germ cells (p < 0.01), and improved pathological changes in the testes (Ma et al., 2009). Echinacoside, which is another newly identifified PhG and is typically known as the main component of echinacea, is abundant in C. tubulosa and possesses vaso-relaxing activity (Yoshikawa et al., 2006). The aphrodisiac mechanisms of C. tubulosa might involve the NO-cGMP signal transduction pathway, with increasing cGMP levels in the corpus cavernosum smooth muscle (He et al., 2009b). Pan and Min (2004) indicated that the combined use of Herba Cistanche extract could prevent adrenal cortical atrophy, which is typically caused by using corticosteroids only. Moreover, C. deserticola extract could reverse the reproductive toxicity in mice induced by hydroxyurea (Gu et al., 2013) and glycoside of Leigongteng (Radix et Rhizoma Tripterygii) (Li et al., 2014). 

According to TCM, Yang-Qi Kidney-Yang Deficiency Syndrome (KDS-Yang) is caused by insuffiffifficient “Yang-Qi” in the kidney. Brieflfly, Yang-Qi is a TCM term and likely indicates mitochondrion-driven biological activities of the human body in the view of biomedical research (Leong et al., 2015). In H9c2 cardiomyocytes, Herba Cistanche was proven to enhance mitochondrial respiration and glutathione antioxidant status (Wong and Ko, 2013). Yang-Qi's deficiencies in TCM resemble those of chronic fatigue syndrome in Western medicine. KDS-Yang symptoms include soreness and weakness of the waist and knees, cold chills, deafness, and tinnitus. Modern studies showed that damage and functional disorders of the hypothalamic-pituitary-target gland axis, including the adrenal gland, thyroid, and gonad, are the main pathological mechanisms of KDS-Yang (Zhao et al., 2013). Gong et al. (2008) investigated the intervention effect of C. deserticola (decoction, 10 g/kg·d) in hydrocortisone-induced KDS-Yang model rats and found that C. deserticola extract could increase body weight, autonomic activity, and swimming time while decreasing post-exercise blood lactic acid (LAC) and blood urea nitrogen (BUN). As described in the Compendium of Materia Medica, Herba Cistanche is mild and would not be extremely abrupt or harsh when treating KDS-Yang. Interestingly, KDS-Yang also leads to low and disordered immune function, and thus, there is a close relationship between treating KDS-Yang and improving immune function (Yim and Ko, 2002). 

Immune-Boosting Effect 

Besides its traditional use, the daily consumption of Herba Cistanche is believed to be the key to people with longevity in some regions of China and Japan where known for longevity oases. Studies have shown that both C. salsa extract and C. tubulosa extract can activate lymphoid cells and increase the killed rate of cancer cells (Maruyama et al., 2009). C. deserticola extract can activate the phagocytic function of macrophages in mice and enhance body immunity (Li et al., 2009). Carbohydrates account for a high proportion of the dry mass of Herba Cistanche. The polysaccharides of C. deserticola are closely related to immunity-enhancing and anti-cancer functions (Xu et al., 2011). Galactitol is one of the monosaccharides in Herba Cistanche with laxative activity (Baishun et al., 2003). Individual compounds such as oligosaccharides present an excellent effect on the spleen activity of mice, increase the phagocytotic activity of macrophages and stimulate the proliferation of antibody-producing cells (Maruyama et al., 2008). Acteoside (10 or 50 mg/kg subcutaneously) significantly inhibits hepatic apoptosis, hepatitis, and lethality in mice with hepatic apoptosis and liver failure induced by D-galactosamine (DGalN) and lipopolysaccharide (LPS) (Xiong et al., 1999). Echinacosideenriched extract of C. tubulosa is effective in preventing dextran sulfate sodium (DSS)-induced colitis in mice (Jia et al., 2014).

Recently, Zhang et al. (2014) discovered that C. deserticola extract could antagonize immune-related senescence and extend the lifespan in SAM-P8 mice. In Zhang’s et al. (2014) study, dietary supplementation with C. deserticola extract can decrease the level of peripheral memory T cells and enhance levels of naive T cells. Additionally, Herba Cistanche aqueous extract was proven to prevent bone loss caused by ovarian hormone deficiency by regulating some bone metabolism-related genes (e.g., Smad1, Smad5, TGF-b1, and TIEG1) (Liang et al., 2011, 2013), and a monoterpene from C. salsa has been identifified as an anti-osteoporotic compound (Yamaguchi et al., 1999). Herba Cistanche helps people better understand the synergistic effect mechanisms of the effective components in TCM. 

Cistanche

REFERENCES 

Baishun, Z., Shuanghou, C., and Xuewen, Z. (2003). Study on the dosage-effect

    relationship of laxative action of galactitol from cistanche deserticola [J]. Chin.

   J. Inform. 12:15.

Chen, H., Jing, F. C., Li, C. L., Tu, P. F., Zheng, Q. S., and Wang,

   Z. H. (2007). Echinacoside prevents the striatal extracellular levels of monoamine neurotransmitters from diminution in 6-hydroxydopamine lesion rats. J. Ethnopharmacol. 114, 285–289. doi: 10.1016/j.jep.2007.07.035 

Chiou, W. F., Lin, L. C., and Chen, C. F. (2004). Acteoside protects endothelial cells against free radical-induced oxidative stress. J. Pharm. Pharmacol. 56, 743–748. doi: 10.1211/0022357023501

Choi, J. G., Moon, M., Jeong, H. U., Kim, M. C., Kim, S. Y., and Oh, M. S. (2011). 

     Cistanches Herba enhances learning and memory by inducing nerve growth factors. Behav. Brain Res. 216, 652–658. doi: 10.1016/j.bbr.2010.09.008

Deng, M., Zhao, J. Y., Ju, X. D., Tu, P. F., Jiang, Y., and Li, Z. B. (2004a). Protective effect of tubuloside B on TNF alpha-induced apoptosis in neuronal cells. Acta Pharmacol. Sin. 25, 1276–1284.

Deng, M., Zhao, J. Y., Tu, P. F., Jiang, Y., Li, Z. B., and Wang, Y. H. (2004b). Echinacoside rescues the SHSY5Y neuronal cells from TNFα-induced apoptosis. Eur. J. Pharmacol. 505, 11–18. doi: 10.1016/j.ejphar.2004.09.059 

Geng, X., Tian, X., Tu, P., and Pu, X. (2007). Neuroprotective effects of echinacoside in the mouse MPTP model of Parkinson’s disease. Eur. J. Pharmacol. 564, 66–74. doi: 10.1016/j.ejphar.2007.01.084 

Gong, M. J., Liu, X. M., and Wang, L. W. (2008). Study on the antifatigue effect of caulis distances on the mice with yang Asthenia. Guid. J. 13, 8–10.

Gu, L., Xiong, W. T., Wang, C., Sun, H. X., Li, G. F., and Liu, X. (2013). Cistanche deserticola decoction alleviates the testicular toxicity induced by hydroxyurea in male mice. Asian J. Androl. 15, 838–840. doi: 10.1038/Aja.2013.73 

Guo, Q., Zhou, Y., Wang, C. J., Huang, Y. M., Lee, Y. T., Su, M. H., et al. (2013). An open-label, nonplacebo-controlled study on Cistanche tubulosa glycoside capsules (Memoregain(R)) for treating moderate Alzheimer’s Disease. Am. J. Alzheimer's Dis. Other Demen. 28, 363–370. doi: 10.1177/1533317513488907 

He, W., Fang, T., and Tu, P. (2009a). Research progress on pharmacological activities of echinacoside. Zhongguo Zhong Yao Za Zhi 34, 476–479. 

He, W. J., Fang, T. H., Ma, X., Zhang, K., Ma, Z. Z., and Tu, P. F. (2009b). Echinacoside elicits endothelium-dependent relaxation in rat aortic rings via a NO-cGMP pathway. Planta Med. 75, 1400–1404. doi: 10.1055/s-0029-1185745 

Jia, Y., Guan, Q., Jiang, Y., Salh, B., Guo, Y., Tu, P., et al. (2014). Amelioration of dextran sulfate sodium-induced colitis in mice by echinacoside-enriched extract of Cistanche tubulosa. Phytother. Res. 28, 110–119. doi: 10.1002/ptr.4967

Jiang, Y., and Tu, P. F. (2009). Analysis of chemical constituents in Cistanche species. J. Chromatogr. 1216, 1970–1979. doi: 10.1016/j.chroma.2008.07.031 

Jin, X. L., and Zhang, Q. R. (1994). Recent progress in the study on chemical constituents of herba Cistanche. Zhongguo Zhong Yao Za Zhi 19, 695–697. 

Karalliedde, L. D., and Kappagoda, C. T. (2009). The challenge of traditional Chinese medicines for allopathic practitioners. Am. J. Physiol. Heart Circ. Physiol. 297, H1967–H1969. doi: 10.1152/ajpheart.00944.2009 

Leong, P. K., Wong, H. S., Chen, J., and Ko, K. M. (2015). Yang/Qi invigoration: an herbal therapy for chronic fatigue syndrome with yang deficiency? Evid. Based Comp. Alternat. Med. 2015:945901. doi: 10.1155/2015/945901 

Li, F., Yang, X., Yang, Y., Guo, C., Zhang, C., Yang, Z., et al. (2013a). The antiosteoporotic activity of echinacoside in ovariectomized rats. Phytomedicine 20, 549–557. doi: 10.1016/j.phymed.2013.01.001

Li, J., Huang, D., and He, L. (2014). Effect of roucongrong (Herba Cistanches Deserticolae) on reproductive toxicity in mice induced by glycoside of Leigongteng (Radix et Rhizoma Tripterygii). J. Tradit. Chin. Med. 34, 324–328. doi: 10.1016/S0254-6272(14)60097-2

Li, X., Ma, Y. Q., Song, Y. X., Shui, J. F., and Li, X. W. (2009). Effect of difffferent plant growth regulators on transplanting survival ratio of Haloxylon ammo dendron seedling and parasitic ratio of Cistanche deserticola. Zhong Yao Cai 32, 1651– 1654. 

Li, X., Zhang, T. C., Qiao, Q., Ren, Z., Zhao, J., Yonezawa, T., et al. (2013b). The complete chloroplast genome sequence of holoparasite Cistanche deserticola (Orobanchaceae) reveals gene loss and horizontal gene transfer from its host Haloxylon ammo dendron (Chenopodiaceae). PLoS ONE 8:e58747. doi: 10.1371/journal.pone.0058747 

Li, Y., Wang, X., Chen, T., Yao, F., Li, C., Tang, Q., et al. (2015). RNA-Seq based de novo transcriptome assembly and gene discovery of cistanche deserticola flfleshy stem. PLoS ONE 10:e0125722. doi: 10.1371/journal.pone.0125722 

Liang, H., Yu, F., Tong, Z., and Huang, Z. (2011). Effect of Cistanches Herba aqueous extract on bone loss in ovariectomized rat. Int. J. Mol. Sci. 12, 5060– 5069. doi: 10.3390/ijms12085060 

Liang, H. D., Yu, F., Tong, Z. H., Zhang, H. Q., and Liang, W. (2013). Cistanches Herba aqueous extract affecting serum BGP and TRAP and bone marrow Smad1 mRNA, Smad5 mRNA, TGF-beta1 mRNA, and TIEG1 mRNA expression levels in osteoporosis disease. Mol. Biol. Rep. 40, 757–763. doi: 10.1007/s11033-012-2065-2 

Lin, L.-W., Hsieh, M.-T., Tsai, F.-H., Wang, W.-H., and Wu, C.-R. (2002). The antinociceptive and anti-inflammatory activity caused by Cistanche deserticola in rodents. J. Ethnopharmacol. 83, 177–182. doi: 10.1016/S0378-8741(02)00147-2

Lin, S., Ye, S., Huang, J., Tian, Y., Xu, Y., Wu, M., et al. (2013). How do Chinese medicines that tonify the kidney inhibit dopaminergic neuron apoptosis? Neural Regen. Res. 8, 2820–2826. 

Luo, L., Aerziguli, T., and Wang, X. W. (2010). Protective effects of glycosides of cistanche on apoptosis of PC12 cells induced by aggregated β-amyloid protein 25-35. Chin J. New Drugs Clin. Rem. 29, 115–118.

Ma, J. J., Zhao, F., and Sun, Y. (2009). The effects of acteoside on nourishing kidney and strengthening Yang in Yang deficient mice. J. Yangzhou Univ. 30, 22–25.

Maruyama, S., Akasaka, T., Yamada, K., and Tachibana, H. (2009). Bioactivity of high-molecular-weight constituents of Cistanche tubulosa. Pharmacology 1, 913–921. 

Maruyama, S., Hashizume, S., Tanji, T., Yamada, K., and Tachibana, H. (2008). Cistanche salsa extract enhanced antibody production in human lymph node lymphocytes. Pharmacology 2, 341–348. 

Motojima, H., Villareal, M. O., Iijima, R., Han, J., and Isoda, H. (2013). Acteoside inhibits type Iota allergy through the down-regulation of Ca/NFAT and JNK MAPK signaling pathways in basophilic cells. J. Nat. Med. 67, 790–798. doi: 10.1007/s11418-013-0753-4

Nan, Z. D., Zeng, K. W., Shi, S. P., Zhao, M. B., Jiang, Y., and Tu, P. F. (2013). Phenylethanoid glycosides with anti-inflammatory activities from the stems of Cistanche deserticola cultured in the Tarim desert. Fitoterapia 89, 167–174. doi: 10.1016/j.fifitote.2013.05.008 

Pan, Y. R., and Min, F. Y. (2004). The influence of the adrenal gland of kidney Yang deficiency animal model after treating Cistanche alcohol extract. J. Pract. Tradit. Chin. Med. 20, 357–357. 

Pharmacopoeia, N. C. O. C. (2000). Pharmacopoeia of the People’s Republic of China. Beijing: The Chemical Industry Publishing House. 

Pharmacopoeia, N. C. O. C. (2005). Pharmacopoeia of the People’s Republic of China. Beijing: The Chemical Industry Publishing House. 

Plant Institute of Chinese Academy of Science (1994). Taxonomical Index of Chinese Higher Plants. Beijing: Publisher of Science, 401. 

Pu, X. P., Song, Z. H., Li, Y. Y., Tu, P. F., and Li, H. N. (2003). Acteoside from Cistanche salsa inhibits apoptosis by 1-methyl-4-phenyl pyridinium ion in cerebellar granule neurons. Planta Med. 69, 65–66. doi: 10.1055/s-2003- 37029 

Qiao, X. Y., Wang, H. L., and Guo, Y. H. (2007). Study on conditions of seed germination of Cistanche. Zhongguo Zhong Yao Za Zhi 32, 1848–1850. 

Sato, T., Kozima, S., Kobayashi, K., and Kobayashi, H. (1985). Pharmacological studies on Cistanchis Herba. I. Effffects of the constituents of distances herba on sex and learning behavior in chronic stress mice (1). Yakugaku Zasshi 105, 1131–1144. 

Shen, H. M., Wang, X. W., Gu, D. T., Li, L. L., and Wang, X. F. (1995). Morphological changes of peripheral blood corpuscles of radiated rats fed with Cistanche. J. Xinjiang Med. Coll. 18, 83–89.

Sheng, G. Q., Pu, X. P., Lei, L., Tu, P. F., and Li, C. L. (2002). Tubuloside B from Cistanche salsa rescues the PC12 neuronal cells from 1-methyl-4- phenyl pyridinium ion-induced apoptosis and oxidative stress. Planta Med. 68, 966–970. doi: 10.1055/s-2002-35667 

Shimoda, H., Tanaka, J., Takahara, Y., Takemoto, K., Shan, S. J., and Su, M. H. (2009). The hypocholesterolemic effects of Cistanche tubulosa extract, a Chinese traditional crude medicine, in mice. Am. J. Chin. Med. 37, 1125–1138. doi: 10.1142/S0192415X09007545 

Snytnikova, O. A., Tsentalovich, Y. P., Stefanova, N. A., Fursova, A., Kaptein, R., Sagdeev, R. Z., et al. (2012). The therapeutic effect of mitochondria-targeted antioxidants SkQ1 and Cistanche deserticola is associated with increased levels of tryptophan and kynurenine in the rat lens. Dokl. Biochem. Biophys. 447, 300–303. doi: 10.1134/S1607672912060087 

Tian, X.-F., and Pu, X.-P. (2005). Phenylethanoid glycosides from Cistanches salsa inhibit apoptosis induced by 1-methyl-4-phenyl pyridinium ion in neurons. J. Ethnopharmacol. 97, 59–63. doi: 10.1016/j.jep.2004.10.014 

Wang, T., Chen, C., Yang, M., Deng, B., Kirby, G. M., and Zhang, X. (2015). Cistanche tubulosa ethanol extract mediates rat sex hormone levels by induction of testicular steroidogenic enzymes. Pharm. Biol. 54, 481–487. doi: 10.3109/13880209.2015.1050114 

Wang, X., Meng, X., and Jiang, X. (2004). Protective effects of glycosides of cistanche on cerebral ischemia-reperfusion damage of brain tissue in CA_1 region of the hippocampus in awake mice. Stroke Nerv. Dis. 10, 325–328. 

Wang, X. W., Jiang, X. Y., Wu, L.-Y., Wang, X. F., and Abdulrahim-Yusup. (2001). Scavenging effects of glycosides of Cistanche on free radicals and its protection against OH·-induced DNA damage in vitro. J. Clin. Pharmacol. 36:4.

Wong, H. S., and Ko, K. M. (2013). Herba Cistanches stimulates cellular glutathione redox cycling by reactive oxygen species generated from mitochondrial respiration in H9c2 cardiomyocytes. Pharm. Biol. 51, 64–73. doi: 10.3109/13880209.2012.710242 

Wu, C. R., Lin, H. C., and Su, M. H. (2014). Reversal by aqueous extracts of Cistanche tubulosa from behavioral deficits in Alzheimer’s disease-like rat model: relevance for amyloid deposition and central neurotransmitter function. BMC Comp. Altern. Med. 14:202. doi: 10.1186/1472-6882-14-202 

Xie, H., Morikawa, T., Matsuda, H., Nakamura, S., Muraoka, O., and Yoshikawa, M. (2006). Monoterpene constituents from Cistanche tubulosachemical structures of kankanosides A-E and alkanol. Chem. Pharm. Bull. (Tokyo) 54, 669–675. doi: 10.1248/CPB.54.669 

Xiong, Q., Hase, K., Tezuka, Y., Namba, T., and Kadota, S. (1999). Acteoside inhibits apoptosis in D-galactosamine and lipopolysaccharide-induced liver injury. Life Sci. 65, 421–430. doi: 10.1016/S0024-3205(99) 00263-5 

Xiong, Q. B., Hase, K., Tezuka, Y., Tani, T., Namba, T., and Kadota, S. (1998). Hepatoprotective activity of phenylethanoids from Cistanche deserticola. Planta Med. 64, 120–125. doi: 10.1055/s-2006-957387 

Xiong, Q. B., Kadota, S., Tani, T., and Namba, T. (1996). Antioxidative effects of phenylethanoids from Cistanche deserticola. Biol. Pharm. Bull. 19, 1580–1585. doi: 10.1248/bob.19.1580

Xu, H., Wei, X. D., Ou, Q., Li, Y., Xu, X. X., Wang, J. T., et al. (2011). Desertliving Cistanche anti-aging action: a comparative study. Heilongjiang Med. Pharm. 34, 1–2.

Yamaguchi, K., Shinohara, C., Kojima, S., Sodeoka, M., and Tsuji, T. (1999). (2E,6R)-8-hydroxy-2,6-dimethyl-2-octanoic acid, a novel anti-osteoporotic monoterpene, isolated from Cistanche salsa. Biosci. Biotechnol. Biochem. 63, 731–735. doi: 10.1271/BBB.63.731 

Yim, T., and Ko, K. (2002). Antioxidant and immunomodulatory activities of Chinese tonifying herbs. Pharm. Biol. 40, 329–335. doi: 10.1076/phbi.40.5.329.8457 

Yoshikawa, M., Matsuda, H., Morikawa, T., Xie, H., Nakamura, S., and Muraoka, O. (2006). Phenylethanoid aminoglycosides and acylated oligo sugars with vasorelaxant activity from Cistanche tubulosa. Bioorg. Med. Chem. 14, 7468–7475. doi: 10.1016/j.bmc.2006.07.018

Zhang, C. Z., Wang, S. X., Zhang, Y., Chen, J. P., and Liang, X. M. (2005). In vitro estrogenic activities of Chinese medicinal plants traditionally used for the management of menopausal symptoms. J. Ethnopharmacol. 98, 295–300. doi: 10.1016/j.jep.2005.01.033 

Zhang, K., Ma, X., He, W., Li, H., Han, S., Jiang, Y., et al. (2014). Extracts of Cistanche deserticola can antagonize immunosenescence and extend the life span in senescence-accelerated mouse prone 8 (SAM-P8) Mice. Evid. Based Comp. Altern. Med. 2014:601383. doi: 10.1155/2014/ 601383 

Zhang, X., Wu, F., Lin, R., Zhang, X., Liu, N., Li, J., et al. (2012). Changes of lung, spleen, and kidney aquaporin-1 in rats with Kidney Yang Deficiency: the “water metabolism theory” in traditional Chinese medicine. Nan Fang Yi Ke Da Xue Xue Bao 32, 1507–1510.

Zhao, L., Wu, H., Qiu, M., Sun, W., Wei, R., Zheng, X., et al. (2013). Metabolic signatures of kidney yang deficiency syndrome and protective effects of two herbal extracts in rats using GC/TOF MS. Evid. Based Comp. Alternat. Med. 2013:540957. doi: 10.1155/2013/540957 

Zhao, Q., Gao, J., Li, W., and Cai, D. (2010). Neurotrophic and neurorescue effects of Echinacoside in the subacute MPTP mouse model of Parkinson’s disease. Brain Res. 1346, 224–236. doi: 10.1016/j.brainres.2010. 05.018 

Zhong, M., Chen, H., Jiang, Y., Tu, P. F., Liu, C. L., Zhang, W. X., et al. (2012). Effects of echinacoside on striatal extracellular levels of amino acid neurotransmitter in cerebral ischemia rats. Chin. Pharmacol. Bull. 28, 361–365. 

CONCLUSION 

Herba Cistanche has been commonly used traditionally for enhancing immunity, sexual health, antioxidation, neuroprotection, and tonic. Various Herba Cistanche products and its derivative are widely used in modern China. The uses of this drug have evolved over nearly 2,000 years, and the demand for Herba Cistanche has grown rapidly in recent years. After long-term use, those compounds with proven pharmacological activity, such as octreotide, and echinacoside, deserve more in-depth study before they truly could improve patient quality of life. With further study, this important TCM is believed to have profound prospects. 

AUTHOR CONTRIBUTIONS 

HL drafted the table. LG and JG designed the figure. ZL and CT drafted and revised the manuscript. 

SUPPLEMENTARY MATERIAL 

The Supplementary Material for this article can be found online at: http://journal.frontiersin.org/article/10.3389/fphar. 2016.00041 

FIGURE S1 | Main biological functions and mechanisms of the active components of Herba Cistanche

The active ingredients isolated from Herba Cistanche have three main biological functions: improvement of brain function, immune-boosting effect, and nourishing aphrodisiac effect. Herba Cistanche extracts are mixtures of multiple active compounds, and a typical traditional Chinese medicine (TCM) recognizes multiple biological targets. Phenylethanoid glycosides (PhGs) have neuroprotective properties in neurodegenerative disease based on their free radical scavenging ability, anti-apoptosis activity, anti-inflammation activity, the increasing amount of brain neurotransmitters, and enhanced SOD activity. A modern use of Herba Cistanche in Chinese herbalism is to treat KDS-Yang, which contributes to fertility problems (including impotence and female infertility) because Herba Cistanche is different from other herbs that often have a more vigorous action. Herba Cistanche regulates the hypothalamic-pituitary-gonad (HPG) and hypothalamic-pituitary-adrenal (PHA) axes, which may induce a smooth and balanced sexual vitality effect. Moreover, phenylethanoid aminoglycosides and acylated oligosaccharides from Herba Cistanche have vasorelaxant activity via the NO-cGMP pathway. Based on clinical and experimental data, activation of the HPA axis increases plasma cytokines and acute-phase protein concentrations. Thus, it can increase phytohemagglutinin-stimulated lymphocyte proliferation and enhance antibody production in response to T-dependent antigens in spleen cells. 

REFERENCES 

Baishun, Z., Shuanghou, C., and Xuewen, Z. (2003). Study on the dosage-effect relationship of laxative action of galactitol from cistanche deserticola [J]. Chin. J. Inform. 12:15.

Chen, H., Jing, F. C., Li, C. L., Tu, P. F., Zheng, Q. S., and Wang, Z. H. (2007). Echinacoside prevents the striatal extracellular levels of monoamine neurotransmitters from diminution in 6-hydroxydopamine lesion rats. J. Ethnopharmacol. 114, 285–289. doi: 10.1016/j.jep.2007.07.035 

Chiou, W. F., Lin, L. C., and Chen, C. F. (2004). Acteoside protects endothelial cells against free radical-induced oxidative stress. J. Pharm. Pharmacol. 56, 743–748. doi: 10.1211/0022357023501 

Choi, J. G., Moon, M., Jeong, H. U., Kim, M. C., Kim, S. Y., and Oh, M. S. (2011). Cistanches Herba enhances learning and memory by inducing nerve growth factors. Behav. Brain Res. 216, 652–658. doi: 10.1016/j.bbr.2010.09.008 

Deng, M., Zhao, J. Y., Ju, X. D., Tu, P. F., Jiang, Y., and Li, Z. B. (2004a). Protective effect of tubuloside B on TNF alpha-induced apoptosis in neuronal cells. Acta Pharmacol. Sin. 25, 1276–1284.

Deng, M., Zhao, J. Y., Tu, P. F., Jiang, Y., Li, Z. B., and Wang, Y. H. (2004b). Echinacoside rescues the SHSY5Y neuronal cells from TNFα-induced apoptosis. Eur. J. Pharmacol. 505, 11–18. doi: 10.1016/j.ejphar.2004.09.059 

Geng, X., Tian, X., Tu, P., and Pu, X. (2007). Neuroprotective effects of echinacoside in the mouse MPTP model of Parkinson’s disease. Eur. J. Pharmacol. 564, 66–74. doi: 10.1016/j.ejphar.2007.01.084 

Gong, M. J., Liu, X. M., and Wang, L. W. (2008). Study on the antifatigue effect of caulis distances on the mice with yang Asthenia. Guid. J. 13, 8–10.

Gu, L., Xiong, W. T., Wang, C., Sun, H. X., Li, G. F., and Liu, X. (2013). Cistanche deserticola decoction alleviates the testicular toxicity induced by hydroxyurea in male mice. Asian J. Androl. 15, 838–840. doi: 10.1038/Aja.2013.73

Guo, Q., Zhou, Y., Wang, C. J., Huang, Y. M., Lee, Y. T., Su, M. H., et al. (2013). An open-label, nonplacebo-controlled study on Cistanche tubulosa glycoside capsules (Memoregain(R)) for treating moderate Alzheimer’s Disease. Am. J. Alzheimer's Dis. Other Demen. 28, 363–370. doi: 10.1177/1533317513488907 

He, W., Fang, T., and Tu, P. (2009a). Research progress on pharmacological activities of echinacoside. Zhongguo Zhong Yao Za Zhi 34, 476–479.

He, W. J., Fang, T. H., Ma, X., Zhang, K., Ma, Z. Z., and Tu, P. F. (2009b). Echinacoside elicits endothelium-dependent relaxation in rat aortic rings via a NO-cGMP pathway. Planta Med. 75, 1400–1404. doi: 10.1055/s-0029-1185745

Jia, Y., Guan, Q., Jiang, Y., Salh, B., Guo, Y., Tu, P., et al. (2014). Amelioration of dextran sulfate sodium-induced colitis in mice by echinacoside-enriched extract of Cistanche tubulosa. Phytother. Res. 28, 110–119. doi: 10.1002/ptr.4967 

Jiang, Y., and Tu, P. F. (2009). Analysis of chemical constituents in Cistanche species. J. Chromatogr. 1216, 1970–1979. doi: 10.1016/j.chroma.2008.07.031

Jin, X. L., and Zhang, Q. R. (1994). Recent progress in the study on chemical constituents of herba Cistanche. Zhongguo Zhong Yao Za Zhi 19, 695–697. 

Karalliedde, L. D., and Kappagoda, C. T. (2009). The challenge of traditional Chinese medicines for allopathic practitioners. Am. J. Physiol. Heart Circ. Physiol. 297, H1967–H1969. doi: 10.1152/ajpheart.00944.2009 

Leong, P. K., Wong, H. S., Chen, J., and Ko, K. M. (2015). Yang/Qi invigoration: an herbal therapy for chronic fatigue syndrome with yang deficiency? Evid. Based Comp. Alternat. Med. 2015:945901. doi: 10.1155/2015/945901

Li, F., Yang, X., Yang, Y., Guo, C., Zhang, C., Yang, Z., et al. (2013a). The antiosteoporotic activity of echinacoside in ovariectomized rats. Phytomedicine 20, 549–557. doi: 10.1016/j.phymed.2013.01.001 

Li, J., Huang, D., and He, L. (2014). Effect of roucongrong (Herba Cistanches Deserticolae) on reproductive toxicity in mice induced by glycoside of Leigongteng (Radix et Rhizoma Tripterygii). J. Tradit. Chin. Med. 34, 324–328. doi: 10.1016/S0254-6272(14)60097-2 

Li, X., Zhang, T. C., Qiao, Q., Ren, Z., Zhao, J., Yonezawa, T., et al. (2013b). The complete chloroplast genome sequence of holoparasite Cistanche deserticola (Orobanchaceae) reveals gene loss and horizontal gene transfer from its host Haloxylon ammo dendron (Chenopodiaceae). PLoS ONE 8:e58747. doi: 10.1371/journal.pone.0058747 

Li, Y., Wang, X., Chen, T., Yao, F., Li, C., Tang, Q., et al. (2015). RNA-Seq based de novo transcriptome assembly and gene discovery of cistanche deserticola flfleshy stem. PLoS ONE 10:e0125722. doi: 10.1371/journal.pone.0125722 

Liang, H., Yu, F., Tong, Z., and Huang, Z. (2011). Effect of Cistanches Herba aqueous extract on bone loss in ovariectomized rat. Int. J. Mol. Sci. 12, 5060– 5069. doi: 10.3390/ijms12085060 

Liang, H. D., Yu, F., Tong, Z. H., Zhang, H. Q., and Liang, W. (2013). Cistanches Herba aqueous extract affecting serum BGP and TRAP and bone marrow Smad1 mRNA, Smad5 mRNA, TGF-beta1 mRNA, and TIEG1 mRNA expression levels in osteoporosis disease. Mol. Biol. Rep. 40, 757–763. doi: 10.1007/s11033-012-2065-2

Lin, L.-W., Hsieh, M.-T., Tsai, F.-H., Wang, W.-H., and Wu, C.-R. (2002). The antinociceptive and anti-inflammatory activity caused by Cistanche deserticola in rodents. J. Ethnopharmacol. 83, 177–182. doi: 10.1016/S0378-8741(02)00147-2

Lin, S., Ye, S., Huang, J., Tian, Y., Xu, Y., Wu, M., et al. (2013). How do Chinese medicines that tonify the kidney inhibit dopaminergic neuron apoptosis? Neural Regen. Res. 8, 2820–2826.

Luo, L., Aerziguli, T., and Wang, X. W. (2010). Protective effects of glycosides of cistanche on apoptosis of PC12 cells induced by aggregated β-amyloid protein 25-35. Chin J. New Drugs Clin. Rem. 29, 115–118. 

Ma, J. J., Zhao, F., and Sun, Y. (2009). The effects of acteoside on nourishing kidney and strengthening Yang in Yang deficient mice. J. Yangzhou Univ. 30, 22–25.

Maruyama, S., Akasaka, T., Yamada, K., and Tachibana, H. (2009). Bioactivity of high-molecular-weight constituents of Cistanche tubulosa. Pharmacology 1, 913–921. 

Maruyama, S., Hashizume, S., Tanji, T., Yamada, K., and Tachibana, H. (2008). Cistanche salsa extract enhanced antibody production in human lymph node lymphocytes. Pharmacology 2, 341–348. 

Motojima, H., Villareal, M. O., Iijima, R., Han, J., and Isoda, H. (2013). Acteoside inhibits type Iota allergy through the down-regulation of Ca/NFAT and JNK MAPK signaling pathways in basophilic cells. J. Nat. Med. 67, 790–798. doi: 10.1007/s11418-013-0753-4

Nan, Z. D., Zeng, K. W., Shi, S. P., Zhao, M. B., Jiang, Y., and Tu, P. F. (2013). Phenylethanoid glycosides with anti-inflammatory activities from the stems of Cistanche deserticola cultured in the Tarim desert. Fitoterapia 89, 167–174. doi: 10.1016/j.fifitote.2013.05.008

Pan, Y. R., and Min, F. Y. (2004). The influence of the adrenal gland of kidney Yang deficiency animal model after treating Cistanche alcohol extract. J. Pract. Tradit. Chin. Med. 20, 357–357. 

Pharmacopoeia, N. C. O. C. (2000). Pharmacopoeia of the People’s Republic of China. Beijing: The Chemical Industry Publishing House. 

Pharmacopoeia, N. C. O. C. (2005). Pharmacopoeia of the People’s Republic of China. Beijing: The Chemical Industry Publishing House. 

Plant Institute of Chinese Academy of Science (1994). Taxonomical Index of Chinese Higher Plants. Beijing: Publisher of Science, 401. 

Pu, X. P., Song, Z. H., Li, Y. Y., Tu, P. F., and Li, H. N. (2003). Acteoside from Cistanche salsa inhibits apoptosis by 1-methyl-4-phenyl pyridinium ion in cerebellar granule neurons. Planta Med. 69, 65–66. doi: 10.1055/s-2003- 37029 

Qiao, X. Y., Wang, H. L., and Guo, Y. H. (2007). Study on conditions of seed germination of Cistanche. Zhongguo Zhong Yao Za Zhi 32, 1848–1850.

Sato, T., Kozima, S., Kobayashi, K., and Kobayashi, H. (1985). Pharmacological studies on Cistanchis Herba. I. Effffects of the constituents of distances herba on sex and learning behavior in chronic stress mice (1). Yakugaku Zasshi 105, 1131–1144.

Shen, H. M., Wang, X. W., Gu, D. T., Li, L. L., and Wang, X. F. (1995). Morphological changes of peripheral blood corpuscles of radiated rats fed with Cistanche. J. Xinjiang Med. Coll. 18, 83–89. 

Sheng, G. Q., Pu, X. P., Lei, L., Tu, P. F., and Li, C. L. (2002). Tubuloside B from Cistanche salsa rescues the PC12 neuronal cells from 1-methyl-4- phenyl pyridinium ion-induced apoptosis and oxidative stress. Planta Med. 68, 966–970. doi: 10.1055/s-2002-35667

Shimoda, H., Tanaka, J., Takahara, Y., Takemoto, K., Shan, S. J., and Su, M. H. (2009). The hypocholesterolemic effects of Cistanche tubulosa extract, a Chinese traditional crude medicine, in mice. Am. J. Chin. Med. 37, 1125–1138. doi: 10.1142/S0192415X09007545

Snytnikova, O. A., Tsentalovich, Y. P., Stefanova, N. A., Fursova, A., Kaptein, R., Sagdeev, R. Z., et al. (2012). The therapeutic effect of mitochondria-targeted antioxidants SkQ1 and Cistanche deserticola is associated with increased levels of tryptophan and kynurenine in the rat lens. Dokl. Biochem. Biophys. 447, 300–303. doi: 10.1134/S1607672912060087

Tian, X.-F., and Pu, X.-P. (2005). Phenylethanoid glycosides from Cistanches salsa inhibit apoptosis induced by 1-methyl-4-phenyl pyridinium ion in neurons. J. Ethnopharmacol. 97, 59–63. doi: 10.1016/j.jep.2004.10.014 

Wang, T., Chen, C., Yang, M., Deng, B., Kirby, G. M., and Zhang, X. (2015). Cistanche tubulosa ethanol extract mediates rat sex hormone levels by induction of testicular steroidogenic enzymes. Pharm. Biol. 54, 481–487. doi: 10.3109/13880209.2015.1050114 

Wang, X., Meng, X., and Jiang, X. (2004). Protective effects of glycosides of cistanche on cerebral ischemia-reperfusion damage of brain tissue in CA_1 region of the hippocampus in awake mice. Stroke Nerv. Dis. 10, 325–328.

Wang, X. W., Jiang, X. Y., Wu, L.-Y., Wang, X. F., and Abdulrahim-Yusup. (2001). Scavenging effects of glycosides of Cistanche on free radicals and its protection against OH·-induced DNA damage in vitro. J. Clin. Pharmacol. 36:4. 

Wong, H. S., and Ko, K. M. (2013). Herba Cistanches stimulates cellular glutathione redox cycling by reactive oxygen species generated from mitochondrial respiration in H9c2 cardiomyocytes. Pharm. Biol. 51, 64–73. doi: 10.3109/13880209.2012.710242 

Wu, C. R., Lin, H. C., and Su, M. H. (2014). Reversal by aqueous extracts of Cistanche tubulosa from behavioral deficits in Alzheimer’s disease-like rat model: relevance for amyloid deposition and central neurotransmitter function. BMC Comp. Altern. Med. 14:202. doi: 10.1186/1472-6882-14-202 

cistanche

How do Chinese medicines that tonify the kidney inhibit dopaminergic neuron apoptosis? Neural Regen. Res. 8, 2820–2826. Luo, L., Aerziguli, T., and Wang, X. W. (2010). 

Protective effects of glycosides of cistanche on apoptosis of PC12 cells induced by aggregated β-amyloid protein 25-35. Chin J. New Drugs Clin. Rem. 29, 115–118. Ma, J. J., Zhao, F., and Sun, Y. (2009). 

The effects of acteoside on nourishing kidney and strengthening Yang in Yang deficient mice. J. Yangzhou Univ. 30, 22–25. Maruyama, S., Akasaka, T., Yamada, K., and Tachibana, H. (2009). Bioactivity of high-molecular-weight constituents of Cistanche tubulosa. Pharmacology 1, 913–921. 

Maruyama, S., Hashizume, S., Tanji, T., Yamada, K., and Tachibana, H. (2008). Cistanche salsa extract enhanced antibody production in human lymph node lymphocytes. 

Pharmacology 2, 341–348. Motojima, H., Villareal, M. O., Iijima, R., Han, J., and Isoda, H. (2013).

 Acteoside inhibits type Iota allergy through the down-regulation of Ca/NFAT and JNK MAPK signaling pathways in basophilic cells. J. Nat. Med. 67, 790–798. doi: 10.1007/s11418-013-0753-4 Nan, Z. D., Zeng, K. W., Shi, S. P., Zhao, M. B., Jiang, Y., and Tu, P. F. (2013). 

Phenylethanoid glycosides with anti-inflammatory activities from the stems of Cistanche deserticola cultured in the Tarim desert. Fitoterapia 89, 167–174. doi: 10.1016/j.fifitote.2013.05.008 Pan, Y. R., and Min, F. Y. (2004). 

The influence of the adrenal gland of kidney Yang deficiency animal model after treating Cistanche alcohol extract. J. Pract. Tradit. Chin. Med. 20, 357–357. Pharmacopoeia, N. C. O. C. (2000). Pharmacopoeia of the People’s Republic of China. Beijing: The Chemical Industry Publishing House. Pharmacopoeia, N. C. O. C. (2005). 

Pharmacopoeia of the People’s Republic of China. Beijing: The Chemical Industry Publishing House. Plant Institute of Chinese Academy of Science (1994). 

Taxonomical Index of Chinese Higher Plants. Beijing: Publisher of Science, 401. Pu, X. P., Song, Z. H., Li, Y. Y., Tu, P. F., and Li, H. N. (2003). Acteoside from Cistanche salsa inhibits apoptosis by 1-methyl-4-phenyl pyridinium ion in cerebellar granule neurons. Planta Med. 69, 65–66. doi: 10.1055/s-2003- 37029 Qiao, X. Y., Wang, H. L., and Guo, Y. H. (2007). 

Study on conditions of seed germination of Cistanche. Zhongguo Zhong Yao Za Zhi 32, 1848–1850. Sato, T., Kozima, S., Kobayashi, K., and Kobayashi, H. (1985). Pharmacological studies on Cistanchis Herba. I. Effffects of the constituents of distances herba on sex and learning behavior in chronic stress mice (1). 

Yakugaku Zasshi 105, 1131–1144. Shen, H. M., Wang, X. W., Gu, D. T., Li, L. L., and Wang, X. F. (1995). Morphological changes of peripheral blood corpuscles of radiated rats fed with Cistanche. J. Xinjiang Med. Coll. 18, 83–89. Sheng, G. Q., Pu, X. P., Lei, L., Tu, P. F., and Li, C. L. (2002). Tubuloside B from Cistanche salsa rescues the PC12 neuronal cells from 1-methyl-4- phenyl pyridinium ion-induced apoptosis and oxidative stress. Planta Med. 68, 966–970. doi: 10.1055/s-2002-35667 Shimoda, H., Tanaka, J., Takahara, Y., Takemoto, K., Shan, S. J., and Su, M. H. (2009).

 The hypocholesterolemic effects of Cistanche tubulosa extract, a Chinese traditional crude medicine, in mice. 

Am. J. Chin. Med. 37, 1125–1138. doi: 10.1142/S0192415X09007545 Snytnikova, O. A., Tsentalovich, Y. P., Stefanova, N. A., Fursova, A., Kaptein, R., Sagdeev, R. Z., et al. (2012). 

The therapeutic effect of mitochondria-targeted antioxidants SkQ1 and Cistanche deserticola is associated with increased levels of tryptophan and kynurenine in the rat lens. Dokl. Biochem. Biophys. 447, 300–303. doi: 10.1134/S1607672912060087 Tian, X.-F., and Pu, X.-P. (2005).

 Phenylethanoid glycosides from Cistanches salsa inhibit apoptosis induced by 1-methyl-4-phenyl pyridinium ion in neurons. J. Ethnopharmacol. 97, 59–63. doi: 10.1016/j.jep.2004.10.014 Wang, T., Chen, C., Yang, M., Deng, B., Kirby, G. M., and Zhang, X. (2015). 

Cistanche tubulosa ethanol extract mediates rat sex hormone levels by induction of testicular steroidogenic enzymes. 

Pharm. Biol. 54, 481–487. doi: 10.3109/13880209.2015.1050114 Wang, X., Meng, X., and Jiang, X. (2004). Protective effects of glycosides of cistanche on cerebral ischemia-reperfusion damage of brain tissue in CA_1 region of the hippocampus in awake mice.

Stroke Nerv. Dis. 10, 325–328. Wang, X. W., Jiang, X. Y., Wu, L.-Y., Wang, X. F., and Abdulrahim-Yusup. (2001). Scavenging effects of glycosides of Cistanche on free radicals and its protection against OH·-induced DNA damage in vitro. J. Clin. Pharmacol. 36:4. Wong, H. S., and Ko, K. M. (2013). 

Herba Cistanches stimulates cellular glutathione redox cycling by reactive oxygen species generated from mitochondrial respiration in H9c2 cardiomyocytes. Pharm. Biol. 51, 64–73. doi: 10.3109/13880209.2012.710242 Wu, C. R., Lin, H. C., and Su, M. H. (2014). 

Reversal by aqueous extracts of Cistanche tubulosa from behavioral deficits in Alzheimer’s disease-like rat model: relevance for amyloid deposition and central neurotransmitter function. BMC Comp. Altern. Med. 14:202. doi: 10.1186/1472-6882-14-202 

Xie, H., Morikawa, T., Matsuda, H., Nakamura, S., Muraoka, O., and Yoshikawa, M. (2006). Monoterpene constituents from Cistanche tubulosachemical structures of kankanosides A-E and alkanol. Chem. Pharm. Bull. (Tokyo) 54, 669–675. doi: 10.1248/CPB.54.669 Xiong, Q., Hase, K., Tezuka, Y., Namba, T., and Kadota, S. (1999).

Acteoside inhibits apoptosis in D-galactosamine and lipopolysaccharide-induced liver injury. Life Sci. 65, 421–430. doi: 10.1016/S0024-3205(99) 00263-5 Xiong, Q. B., Hase, K., Tezuka, Y., Tani, T., Namba, T., and Kadota, S. (1998). 

Hepatoprotective activity of phenylethanoids from Cistanche deserticola. Planta Med. 64, 120–125. doi: 10.1055/s-2006-957387 Xiong, Q. B., Kadota, S., Tani, T., and Namba, T. (1996). Antioxidative effects of phenylethanoids from Cistanche deserticola. Biol. Pharm. Bull. 19, 1580–1585. doi: 10.1248/bob.19.1580 Xu, H., Wei, X. D., Ou, Q., Li, Y., Xu, X. X., Wang, J. T., et al. (2011). 

Desertliving Cistanche anti-aging action: a comparative study. Heilongjiang Med. Pharm. 34, 1–2. Yamaguchi, K., Shinohara, C., Kojima, S., Sodeoka, M., and Tsuji, T. (1999). (2E,6R)-8-hydroxy-2,6-dimethyl-2-octanoic acid, a novel anti-osteoporotic monoterpene, isolated from Cistanche salsa. Biosci. Biotechnol. Biochem. 63, 731–735. doi: 10.1271/BBB.63.731 Yim, T., and Ko, K. (2002). Antioxidant and immunomodulatory activities of Chinese tonifying herbs. Pharm. Biol. 40, 329–335. doi: 10.1076/phobia.40.5.329.8457 Yoshikawa, M., Matsuda, H., Morikawa, T., Xie, H., Nakamura, S., and Muraoka, O. (2006).

 Phenylethanoid aminoglycosides and acylated oligo sugars with vasorelaxant activity from Cistanche tubulosa. Bioorg. Med. Chem. 14, 7468–7475. doi: 10.1016/j.bmc.2006.07.018 Zhang, C. Z., Wang, S. X., Zhang, Y., Chen, J. P., and Liang, X. M. (2005). 

In vitro estrogenic activities of Chinese medicinal plants traditionally used for the management of menopausal symptoms.

J. Ethnopharmacol. 98, 295–300. doi: 10.1016/j.jep.2005.01.033 Zhang, K., Ma, X., He, W., Li, H., Han, S., Jiang, Y., et al. (2014). Extracts of Cistanche deserticola can antagonize immunosenescence and extend the life span in senescence-accelerated mouse prone 8 (SAM-P8) Mice. Evid. Based Comp. Altern. Med. 2014:601383. doi: 10.1155/2014/ 601383 Zhang, X., Wu, F., Lin, R., Zhang, X., Liu, N., Li, J., et al. (2012). Changes of lung, spleen, and kidney aquaporin-1 in rats with Kidney Yang Deficiency: the “water metabolism theory” in traditional Chinese medicine. 

Nan Fang Yi Ke Da Xue Xue Bao 32, 1507–1510. Zhao, L., Wu, H., Qiu, M., Sun, W., Wei, R., Zheng, X., et al. (2013). Metabolic signatures of kidney yang deficiency syndrome and protective effects of two herbal extracts in rats using GC/TOF MS. Evid. Based Comp. Alternat. Med. 2013:540957. doi: 10.1155/2013/540957 Zhao, Q., Gao, J., Li, W., and Cai, D. (2010). 

Neurotrophic and neurorescue effects of Echinacoside in the subacute MPTP mouse model of Parkinson’s disease. Brain Res. 1346, 224–236. doi: 10.1016/j.brainres.2010. 05.018 Zhong, M., Chen, H., Jiang, Y., Tu, P. F., Liu, C. L., Zhang, W. X., et al. (2012). Effects of echinacoside on striatal extracellular levels of amino acid neurotransmitter in cerebral ischemia rats. Chin. Pharmacol. Bull. 28, 361–365. 

Conflflict of Interest Statement: 

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. Copyright © 2016 Li, Lin, Gu, Gao and Tzeng. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution, or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, following accepted academic practice. No use, distribution, or reproduction is permitted which does not comply with these terms. 


For more information:1950477648nn@gmail.com

You Might Also Like