​12 Renoprotectiive Natural Plant Compounds You Need To Know

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Part Ⅰ: Potential Therapeutic Effects of Natural Plant Compounds in Kidney Disease

Lorena Avila-Carrasco, Elda Araceli García-Mayorga & et al.

1. Allicin (Diallyl Thiosulfinate)

Renoprotective Plants: Allicin (Diallyl Thiosulfinate)

The main bioactive constituents of garlic (Allium sativum L.)are organosulfur compounds (OSCs). Among these compounds, the most plentiful sulfur composite contained in fresh and dry garlic is allin (S-allyl-1-cysteine sulfoxide) [60,61]. Allin can rapidly change into allicin (diallyl thiosulfinate) [61], which has been described as a major OSC and has been reported to be one of the primary substances responsible for antiviral activity (33), immunomodulatory, anti-inflammatory [62], antioxidant [63], and other pharmacological properties [61]. Allin also contains non-sulfur constituents that probably have synergistic or additive properties with OSCs [64].

A randomized double-blind clinical trial study evaluated the effect of garlic extract on the serum inflammatory markers of 42 subjects undergoing peritoneal dialysis(PD), a renal failure therapy. The patients received a dose of 400mg of a standardized garlic extract, which was made in the shape of tablets including 1 mg (1000 mcg)of allin. The dosing scheme in the cases group (garlic extract group)was twice a day for 8 weeks, while the control group received standard treatments plus a placebo during the same period. The results showed that in the patients who received the garlic extract, the inflammatory markers IL-6, C reactive protein (CRP), and the erythrocyte sedimentation rate (ESR)were all significantly reduced, while in the placebo group, a significant decrease was only observed in I-6. However, the assessment of these effects in larger trials is strongly recommended [4].

2. Astaxanthin

Renoprotective Plants: Astaxanthin

Xanthophyll carotenoid colorant has beneficial properties, including anticancer, antioxidant, and anti-inflammatory properties. The most common source of astaxanthin(AST;3,3'-dihydroxy-β,β'-carotene-4,4'-dione) as used in nutritional supplements is obtained from Haematococcus alga [65]. The Food and Drug Administration (FDA)of the United States of America has accepted astaxanthin as a nutraceutical [66]. Studies in humans have discovered notable decreases in OS, dyslipidemia, and inflammatory markers after oral administration of astaxanthin. A clinical evaluation of gastric inflammatory biomarkers was conducted in subjects with functional dyspepsia treated with astaxanthin and revealed a significant increase in CD4+ cells and a decrease in CD8+T cells in 21 patients with Helicobacter pylori(H.pylori) treated with 40 mg of astaxanthin daily and 23 patients were administered a placebo, so the authors suggested that these differences indicated a greater change to a humoral immune response instead of a cytotoxic response [67]. Moreover, they explained that in animal models, where the diet can be standardized without antioxidants, astaxanthin had a tremendous effect on inflammation and on the density of H. pylori [68].

Likewise, a randomized placebo-controlled trial was conducted to investigate the possible action of astaxanthin administration on lipid peroxidation, adiponectin levels, glycemic control, anthropometric indices, and insulin sensitivity in subjects with T2DM, which is a common cause and driver of kidney damage. In the study group, after 8 weeks of 8 mg of astaxanthin administration, the serum adiponectin concentration increased and there was a reduction in visceral body fat mass (p<0.01), serum triglycerides, very-low-density lipoprotein cholesterol (VLDL-C)levels, and systolic blood pressure [5]. The investigators suggested that astaxanthin may provide vascular benefits and reduce the indicators of OS and inflammation [69]; however, their results showed that 12 mg oral astaxanthin/day for 12 months had no great effect on arterial stiffness, OS, or inflammation in renal transplant recipients |70]. Nevertheless, it has been proven in animal models that astaxanthin has a protective effect on kidney damage by regulating inflammation (inducing CD8+ T cells)[71] and oxidative stress-related NRF2/KEAP1 and ROS pathways [72]. Thus, although astaxanthin has demonstrated antioxidant, anti-inflammatory, and vascular-protective effects on different pathologies, more studies would be interesting to elucidate its capacity to improve CKD pathogenesis in human beings.

3. Baicalin

Renoprotective Plants: Baicalin

It is a flavone glycoside isolated from the roots of Scutellaria baicalensis. Clinical studies with baicalin as an adjunctive treatment have targeted the protective functions in liver fibrosis, ulcerative colitis, and diabetes mellitus [73,74]. Many studies have researched the potential of baicalin in the management of subjects with early diabetic renal injury |75]. The effect of baicalin was analyzed in subjects with diabetic nephropathy at a dose of 800 mg three times per day, whereas the control group received a placebo. Both groups were treated and studied for 6 months. The results indicated that baicalin had the potential to decrease the level of proteinuria and improve the kidney function of the diabetic subjects since after taking baicalin therapy, the superoxide dismutase (SOD)and glutathione peroxidase (GSH-px)concentrations of patients were clearly elevated, and the aldose reductase(AR)activity, NF-kB, and vascular endothelial growth factor (VEGF) content reduced considerably. These results demonstrated that baicalin at a dose of 800 mg three times a day can reduce renal vascular permeability, enhance the kidney function of subjects with diabetic nephropathy, and delay the progress of diabetic nephropathy via the polyol pathway, and the antioxidative stress, anti-inflammatory, and other pathways. Further studies are needed to evaluate the nephroprotective effects of baicalin through other mechanisms [8].

A clinical study aimed to evaluate the actions of baicalin on AKI in pediatric sepsis. This clinical investigation included 50 pediatric patients with a diagnosis of sepsis, 25 of whom were given an adjunctive treatment of oral baicalin for 15 days and the other 25 patients received only standard therapies. Their results showed that neither the blood urea nitrogen (BUN)nor the serum creatinine concentrations of the control group changed significantly after basic therapy, but they decreased considerably in the baicalin adjunctive therapy group. It can be assumed, based on these two indices, that the renal function of the baicalin group improved, probably due to the baicalin adjunctive therapy. Therefore, baicalin may decrease AKI in pediatric patients with sepsis. Although this study demonstrated the protective effect of baicalin against AKIin this study group, shown as a decrease in BUN and creatinine levels, the authors did not report the dose administered and therefore the appropriate dosage and probable complications need to be evaluated in subsequent studies [76].

4. Betalain

Renoprotective Plants: Betalain

Another NPC with interesting properties in renal disease is betalain. Betalains are divided into two groups: betacyanins, which produce red tones and are formed by condensation of a cyclo-DOPA (dihydroxyphenylalanine)structure with betalamic acid, and betaxanthines, which produce yellow coloration and are synthesized from different amino compounds and balsamic acid [77]. A pilot crossover clinical trial evaluated whether dietary administration of a betalain-rich extract from red beetroot and a betacyanin-rich extract of Opuntia stricta fruits had the ability to modulate genes/protein expression in coronary artery disease(CAD) patients. CKD is a major risk factor for CAD. Patients with CKD display a high prevalence of hypertension, and cardiovascular disease(CVD) is the leading cause of morbidity and mortality in these patients. The high prevalence of traditional CAD risk factors, such as diabetes and hypertension, means that such patients are also exposed to other non-traditional uremia-related CVD risk factors, including inflammation, oxidative stress, and abnormal calcium-phosphorus metabolism [78].

In a pilot randomized crossover trial, 48 male coronary artery disease patients received about 50 mg of betalain or betacyanin daily for 2 weeks on three occasions separated by washout periods. Patients were divided into three groups depending on the supplement:a betalain-rich supplement of red beetroot (Beta vulgaris), a betacyanin-rich supplement of prickly pear cactus(Opuntia stricta), and a placebo. The results showed that betalain increased sirtuin-1 (SIRT1) and reduced lectin-like oxidized LDL receptor 1 (LOX1)and highly sensitive C reactive protein (hs-CRP) in the peripheral blood mononuclear cells (PBMCs) of patients. These results may be due to the reduction in OS and inflammation via the antioxidant and anti-inflammatory properties of betalains. Thus, betalains may be promising alternatives for supplementing therapies in OS, inflammation, and aging-associated diseases. However, additional analyses are necessary to gain a deeper understanding of their specific physiological functions [9,79,80].

5. Beetroot Juice

Renoprotective Plants: Beetroot Juice

It's a source of concentrated inorganic nitrates. One study on CKD patients(CKD Stage II-IV according to the K/DOQI (Kidney Outcomes Quality Initiative)guidelines) by Kemmner et al. suggested that the administration of beetroot juice with a nitrate load of 300 mg to nine patients increased nitric oxide(NO) concentrations and reduced the renal resistive index(RRI), which are prognostic markers for cardiovascular mortality, compared with a placebo [10]. This result was more evident among CKD patients with decreased renal function and increased arterial stiffness, who had GFR values below the normal range. This reduced value was mainly caused by diabetic or hypertensive renal impairment, both of which are factors responsible for the subsequent outcome of kidney failure. Compared with the controls, the serum creatinine, potassium, and GFR serum levels did not change considerably after beetroot juice ingestion. The serum potassium concentration/level was similar to the placebo group. The results established the improving action of Beta vulgaris is a helpful therapeutic option on the indicators of renal function, decreasing the gradual rate of kidney damage and subsequent mortality in high-risk groups involving hypertensive and diabetic patients with nephropathy [10].

6. Berberine (BBR)

Renoprotective Plants: Berberine (BBR)

It is an isoquinoline alkaloid and is the main active compound isolated from Rhizoma Coptis and Cortex Phellodendron. New analyses have demonstrated that berberine has numerous pharmacological benefits, such as lowering blood glucose, antioxidant activity, blood lipid regulation, reduced inflammation, and elevated insulin sensitivity, thus improving insulin resistance [81,82]. Recently, it has been described as a potential anti-diabetic nephropathy drug [83]. The urine microalbumin/creatinine ratio (UACR) and GFR are significant indicators used for evaluating the status of diabetic nephropathy. A randomized controlled clinical trial was conducted to look at the effects of berberine affects serum Cys C and UACR in patients with T2DM. The researchers administered berberine at a dose of 0.4 g three times per day for a period of 6 months. Their results showed that berberine improved diabetic kidney disease by reducing UACR and serum Cys C in T2DM patients, and the results were statistically significant. However, the authors mentioned that the number of cases in their study was small and the observation period was not long enough, so it is indispensable to verify the long-term efficacy and safety of berberine in the progression of CKD[11]. Berberine has been shown to protect renal tubular cells against hypoxia/reoxygenation injury via Sirt1 [84].

7.Cordycepin

Renoprotective Plants: Cordycepin

It is a naturally derived active compound produced by Cordyceps militaris, belonging to the Clavicipitaceae family. It is a fungus with a long history of common use in traditional medicine and its specific compound, cordycepin, has several health-promoting properties, including anticancer, anti-inflammatory, immunomodulatory, antidiabetic, and antiobesity effects [85-87]. Furthermore, antidiabetic and nephroprotective effects have been attributed to cordycepin in experimental studies [88]. In a clinical study with CKD patients, Cordyceps militaris was administered at 100 mg daily and compared with a placebo (control group). Cordyceps militaris decreased the protein concentration of TLR4, NF-kB p65, COX2, I-1β, and TNF-α. Their results showed that eGFR was considerably improved compared with the control group after 3 months of treatment. This showed that Cordyceps militaris improved the eGFR of CKD patients, and the outcomes suggested that Cordyceps militaris ameliorated kidney function and controlled blood levels of urinal protein, BUN, and creatinine. This study provided support for the possibility that Cordyceps militaris controlled CKDevolution by controlling the TLR4/NF-kB redox signaling pathway [12].

8. Curcumin

Renoprotective Plants: Curcumin

It is a component of turmeric(Curcuma longa). Curcumin (diferuloylmethane)has been shown to be a TNF blocker in vitro and in vivo; nevertheless, only a limited number of analyses have confirmed that curcumin is efficient at reducing TGF-β, IL-8, and TNF-c levels in preclinical [89] and clinical studies[90]. There are several causes involved in the pathogenesis of diabetic renal damage, but TGF-β is considered to be a key player in the progress of actions towards ESRD.In a randomized double-blind placebo-controlled study, the effects of turmeric on TGF-β, IL-8, and TNF-α levels, as well as proteinuria in the urine and serum, were investigated in patients with T2DM nephropathy (n= 20) and a control group (n=20). Individually, the test group subjects were given one capsule containing 500 mg turmeric,22.1 mg of which was the active component curcumin, administered with each meal(three capsules daily) for 2months. Their results demonstrated that serum TGF-βand IL-8 values were considerably lower post-turmeric administration and that short-term turmeric supplementation can reduce proteinuria. Furthermore, they did not report any adverse effects associated with turmeric intake during the 2-month trial duration [17]. The increased ROS may induce IL-8 production and result in reduced glutathione levels, which may be due to increased OS caused by inflammation in ESRD patients with and without diabetes mellitus 191]. In addition, redox imbalance contributes importantly to TGF-βproduction [47], which has long been considered a key mediator of renal fibrosis.

Another study suggested the possible efficacy and safety of turmeric in reducing uremic pruritus(UP) and hs-CRP in ESRD patients. Nevertheless, the authors described that larger sample size and a longer therapy period would be required to additionally confirm the long-term efficacy and safety of adding turmeric in the hemodialysis (HD)population [18]. A review showed that curcumin, as an antioxidant, decreased renal inflammation and could prevent the deleterious complications of diabetes [92]. It has been shown that it is a secure auxiliary therapy for improving macroscopic proteinuria in T2DM patients [93].

Other studies have also shown that curcumin was an effective adjuvant therapy for decreasing macroscopic proteinuria, as was shown in a randomized double-blind clinical trial performed on 46 patients with T2DM. In this study, the patients received 500 mg (one capsule) of curcumin three times/day after meals for 16 weeks. [94]. The researchers mention that the range of persistent proteinuria was closely associated with the level of deterioration of creatinine clearance; curcumin reduced creatinine clearance, resulting in slower kidney function impairment and, possibly, a reversal of fibrotic injury [94]Supplementation with 6g of turmeric augmented postprandial serum insulin levels but did not seem to affect plasma glucose levels or the glycemic index in healthy persons. These results suggest that turmeric might stimulate insulin secretion [95]. On the other hand, in a pilot study, researchers demonstrated that curcumin reduced lipid peroxidation in the plasma of individuals with non-diabetic or diabetic proteinuric CKD and enhanced the antioxidant activity in subjects with diabetic proteinuric CKD, demonstrating that dietary administration of turmeric has a potential antioxidant effect in patients with non-diabetic or diabetic proteinuric CKD [15].

Additionally, a randomized placebo-controlled trial examined the effects of curcumin and quercetin on early graft function in 43 dialysis-dependent cadaveric renal recipients. A single capsule of curcumin(480 mg) and quercetin (20 mg) was administered to patients for 1 month after the transplant operation. The instigators of this report concluded that curcumin and quercetin may restore early outcomes in cadaveric kidney transplantation, possibly through activation of heme oxygenase-1 (HO-1)[19]. Likely use of the advantageous properties of these bioflavonoids is the activation of HO-1, an inducible enzyme that produces carbon monoxide. Stimulation of HO-1 in organ transplantation has the capacity to decrease ischemia-reperfusion (IR)damage and alloimmunity. Furthermore, curcumin induced HO-1 mRNA in human proximal tubule renal cells [96], and this induction may be dependent on the nuclear factor erythroid 2-related factor 2 (Nrf2) transcription factor [97].

In the same way, short-term turmeric administration may decrease hematuria, proteinuria, and systolic blood pressure in subjects with relapsed or refractory lupus nephritis, as established in a randomized and placebo-controlled trial of 24 patients with this biopsy-proven pathology. Each patient in the test group was given one capsule for 3 months, providing 500 mg turmeric, 22.1 mg of which was the active element curcumin (three capsules daily). Nevertheless, long-term tests with higher doses of turmeric are required to elucidate its outcomes on the renal function of such patients and the rate of development of CKD of different origins[17]. However, further research is recommended to evaluate the short- and long-term safety and efficacy of curcumin in this study group [98].

9. Epicatechin-3-gallate, Epicatechin, Epigallocatechin

Renoprotective Plants: Epicatechin-3-gallate, Epicatechin, Epigallocatechin

Polyphenolic constituents (from tea plant; Camellia sinensis) have high anti-inflammatory, antioxidant, and antimutagenic properties in various biological systems. Polyphenols display potential beneficial health properties for chronic diseases, including CKD [99]. The majority of ingredients in tea (among the 400 chemicals that have been identified) are polyphenolic compounds, especially flavonoids originating from the tea plant (Camellia sinensis), which is high in catechin(flavonoid subtype). Three major catechins found in green tea have been described: epicatechin, epigallocatechin, and epicatechin-3-gallate (EGCG). The most abundant and extensively investigated catechin is EGCG[99]. In recent times, the potential use of EGCG in the treatment and prevention of numerous renal diseases, which are often related to inflammation and oxidative stress, has been reviewed [100].

The antioxidant, anti-inflammatory, and antiapoptotic activities of EGCG hold strong hope for its use as an alternative approach to the management or prevention of several renal diseases. The beneficial effects of EGCG are mediated by the underlying molecular mechanisms, mainly by direct inhibition of stress or stimulus-induced ROS overproduction; in addition, it could impact the Nrf2-Keap1-Cul-3 complex, resulting in nuclear translocation of free Nrf2, subsequently binding to the antioxidant response element(ARE) inside the promoter region of the cytoprotective genes and those encoding antioxidant enzymes, which are likewise modulated by NF-KB signaling pathways. Nevertheless, the majority of all studies using EGCG or green tea in kidney diseases have been in animal models or cell cultures. Therefore, clinical studies are needed to obtain scientific support for the renoprotective properties of EGCG on renal pathologies [101,102].

In other research, the authors evaluated the possibility of using a mixture of EGCG and amla extract(AE) obtained from Emblica officinalis, an Indian gooseberry, in the treatment of uremic subjects with T2DM. An EGCG/AE tablet was administered orally (one tablet three times a day)to uremic diabetic patients for 3 months, using a total daily dose of 300 mg of EGCG and 300 mg of AE/day. The results showed that 1:1 EGCG/AE improved diabetic biomarkers, antioxidant protection, and the atherogenic index in uremic diabetic subjects. Based on these results, the researchers concluded that EGCG and AE have the potential for adjuvant use in the treatment of diabetic patients in a uremic state [21,103].

10. Pomegranate (Punica granatum)

Renoprotective Plants: Pomegranate (Punica granatum)

A fruit designated as"a medicine in itself" that has long been included in traditional remedies for preventive and therapeutic purposes [83]. It has a high content of polyphenols, alkaloids, and anthocyanins (flavonoid antioxidants), which are highly effective at scavenging free radicals [104,105]. The nephroprotective effects of pomegranate extract on calcium-containing lithiasis development in patients aged 18 to 70 years with recurrent stone formation have been medically reviewed. Daily administration of pomegranate extract stimulated a significant increase in serum paraoxonase (PON1)activity, along with a decrease in calcium oxalate supersaturation. PON1 is an anti-atherosclerotic component associated with high-density lipoprotein (HDL). An important function of PON1 is to prevent the oxidation of both HDL and LDL [106]. Low levels of PON1 have been associated with hypercholesterolemia, diabetes, and vascular diseases. Supported by the aforementioned findings, the researchers suggest that this strategy could potentially control the risk of kidney stone development [23].

11.Resveratrol

Renoprotective Plants: Resveratrol

It is a phenolic substance (a non-flavonoid stilbene polyphenol), and the trans-isomer is considered to be the most biologically active form. Numerous preclinical and clinical analyses have recognized the anti-inflammatory, antidiabetic, hepatoprotective, neuroprotective, anticancer, and antioxidant properties of resveratrol(RSV;3,54'-trihydroxystilbene). Like-wise, supporting in vivo and in vitro tests of RSV in renal damage indicated that it can decrease fibrosis, mesangial expansion, OS, and inflammatory cytokine levels while improving renal structure and function [107]. Furthermore, with the aim of evaluating the actions of RSV administration on Nrf2 and NF-kBexpression in non-dialyzed patients with CKD, the investigators performed a randomized double-blind crossover trial in 20 non-dialyzed patients with CKD, and their results showed that RSV administration at a dose of 500 mg per day for a period of 4 weeks had no antioxidant or anti-inflammatory activity in those subjects [108]. On the other hand, in another randomized double-blind trial, peritoneal dialysis patients were administered a low (150 mg/day) or high(450 mg/day)dose of trans-resveratrol over 12 weeks, resulting in intensification in the average net ultrafiltration (UF)volume and level. Moreover, angiogenesis biomarkers, VEGF, fetal liver kinase-1 (Flk-1), and the angiopoietin(Ang)-2 rate in peritoneal dialysate effluent (PDE)became markedly diminished in patients treated with a high dose of RSV, whereas the levels of angiopoietin receptor (Tie-2) and thrombospondin-1 (Tsp-1)in the effluent were augmented with RSV treatment. This information implied that RSV administration had angiogenesis-enhancing results in PD patients and augmented ultrafiltration renal function [26]. Moreover, RSV treatment significantly decreased serum creatinine concentrations and preserved GFR, suggesting improved renal function. Therefore, the researchers suggested that RSVlowered insulin resistance and OS and increased pAkt: Akt levels in platelets and urinary ortho-tyrosine elimination [25].

Likewise, an analysis was conducted of 24 patients diagnosed with hypertension between 45 and 65 years of age and with underlying endothelial damage who participated in a randomized double-blind placebo-controlled crossover trial. Each patient was administered a single dose of trans-resveratrol (300 mg)or a placebo. Measurements of blood pressure(BP), aortic systolic blood pressure (SBP), and brachial flow-mediated dilation (FMD) were monitored before and 1.5 h after the intervention. The key results reported were that FMD was considerably augmented in female but not male patients administered trans-resveratrol. These results suggest that hypertensive patients with endothelial dysfunction, mainly women and those with high LDL-c, showed an improvement in endothelial function with a single dose of trans-resveratrol, although there were no significant improvements in peripheral and central BP ranges [27,109].

Furthermore, in another randomized double-blind placebo-controlled clinical trial conducted in 60 patients with a diagnosis of T2DM and albuminuria, resveratrol was randomly administered at a dose of 500 mg per day or a placebo for a period of 90 days, and losartan was additionally supplemented at a dose of 12.5 mg per day to all research subjects. Their results showed that the mean urine albumin/creatinine concentrations were significantly reduced in the RSV group, and urinary albumin clearance, fasting plasma glucose (FPG), insulin, homeostasis model evaluation of insulin resistance (HOMA-IR), and glycosylated hemoglobin(HbAlc) all decreased considerably in the RSV group compared with the placebo group, while the antioxidant effect of RSV was estimated by measuring serum levels of SOD1, glutathione peroxidase(GSH-Px), and catalase(CAT). Patients treated with RSV showed significant increases in serum levels of SOD1, GSH-Px, CAT, and NO compared with the placebo, confirming its antioxidant actions. The authors concluded that RSV could be effective as an adjunct to angiotensin receptor blockers(ARBs)to diminish urinary albumin excretion in subjects with diabetic nephropathy [24].

As indicated, the health benefits of RSV seem to be extensive, with the reduced side effects of RSV making it an interesting option for therapeutic use targeting renal damage. However, further research and clinical trials are indispensable for completely comprehending the actions of RSV on renal injury [107,110].

12. Sulforaphane

Renoprotective Plants: Sulforaphane

It is a bioactive component that is a precursor of glucosinolate in cruciferous vegetables, particularly in young broccoli sprouts (BS)[111,112]. The probable actions of sulforaphane (SFN;1-isothiocyanate-4-methyl-sulphinyl butane) in CKD involve the prevention or diminution of structural injury and alterations in renal function; the reduction of proteinuria by moderating inflammation through increased mRNA expression of Nrf2, NADPH quinone oxidoreductase 1 (NQO-1), HO-1, and SOD; and decreasing OS. Moreover, the results of many preclinical models of kidney disease suggest that SFN could act on several pathways in kidney damage, particularly in ameliorating inflammation and OS, and thus could represent a strategy of choice to improve the prognosis of CKD patients by preventing the progression of CKD [113-115].

In the same way, BS supplements have long been commercialized for the promising health benefits of SFN, which induces the NrF2 pathway and the downstream chemoprotective genes, including Phase 2 enzymes. Most commercially available BSsupplements contain BS packaged as glucoraphanin(GR), which is hydrolyzed to SFN by the intestinal microbiota, which synchronously augments the serum activities of Phase 2 enzymes such as NQO1 and glutathione S-transferase (GST), and also Nrf2 signaling, in several human tissues. The researchers suggested that low doses (30 mg per day) of GF have favorable chemoprotective actions in humans [99]. Likewise, the antioxidant effects are attributed to SF, as shown in a randomized placebo-controlled double-blind trial in male patients diagnosed with fatty liver. This research suggested that dietary supplementation with BS extract including the SF precursor GRis likely to be successful in enhancing liver function through reduction of the OS pathway [100]. In the same manner, a clinical study was conducted to evaluate the anti-inflammatory effects of BS powder(BSP)with a high sulforaphane content, in which the researchers analyzed the inflammatory biomarkers in patients diagnosed with T2DM, who were randomly assigned to three treatment groups for 4 weeks. The groups received either 10 g/d BSP(n=27),5g/d BSP(n=29), or a placebo(n=25). The results showed that serum high-sensitive C-reactive protein (hs-CRP)and interleukin-6(IL-6)were lower in Group A(10g/d dose) compared with the control group post-intervention. This indicated that sulforaphane-rich BSP had positive effects on inflammatory biomarkers in patients with T2DM [28]. On the other hand, a clinical study assessed the actions of prolonged supplementation with BS on inflammatory parameters (TNF-α, IL-6, IL-1β, and CRP)in 40 healthy overweight subjects. The treatment phase involved BS administration at a dose of 30g per day for 10 weeks and the follow-up phase was 10 weeks of the habitual diet and free ingestion of BS. The results showed that IL-6 and CRP values reduced considerably throughout the control phase and that the inflammatory marker concentrations were kept low [116]. Additionally, the researchers explored the anti-inflammatory effects of SF in a randomized controlled study in healthy young people and demonstrated the effects of cruciferous vegetables with a high SF content on specific serum inflammatory parameters, particularly the decrease in IL-6, CRP, and soluble TNF receptor (sTNFRI), being careful to mention that these concentrations were higher among persons with GSTM1-null genotypes [117].

13. Cistanche

Cistanche is a parasitic herb that grows in a warm and arid desert environment. it contains rich effective compounds phenylethanoid glycosides such as Echinacoside and acteoside as well as the flavonoids polysaccharides and terpene etc. it has the function of anti-fatigue, improve and regulate the immune system, protect kidney and treating kidney disease, protect liver, anti-inflation, prevent neurons and prevent cerebral ischemic and ischemic reperfusion injury, etc. consume cistanche on a long term basis can also anti-aging, prolong life span effects.

cistanche and cistanche extract improves kidney function