Review Article

Review of Herbal Traditional Chinese Medicine for the Treatment of Diabetic Nephropathy

Table 1

Applications of herbal TCM Preparations in DN.

NameOriginsMethodsResultsPathways

CHYSRadix astragali, Dioscorea nipponica, radix bupleuri, Angelica sinensis, Pyrrosia petiolosa, Polyporus umbellatus, and Hirudo nipponica Type 1 diabetic animal study (STZ + nephrectomized rat)Inhibiting 24 h proteinuria and progressive renal fibrosis (glomerulosclerosis index, tubulointerstitial fibrosis index, and upregulation of ECM), upregulating Smad7, and downregulating TGF-β1, TGF-βR, Smad3 activation, and miRNA-21 [20]

CRCCRhizoma coptidis, Kudzu root, dwarf lilyturf, and loquat leafType 1 diabetic animal study (STZ induced rats)Reducing FBG, BUN, Cr, Upro levels and TGF-β1, and collagen IV expressions and alleviating pathological lesions of kidneyThrough TGF-β1 pathway [21]

CSTRadix astragali, fructus ligustri lucidi,Rhizoma  zedoaria, and honeysuckleType 1 diabetic animal study (STZ induced rats)Decreasing urine mAlb, Scr, BUN, Glu, TG, and TC [22]

DBTAngelica sinensis and Astragalus membranaceus Type 1 diabetic animal study (STZ induced rats)Attenuating the increases in blood glucose, TG and CHO, and TGF-β1 expression in kidneyThrough TGF-β1 way [23, 24]
Cellular study (mesangial cells)Inhibit cell proliferation and expression of LN, FN, and collagen IV

DSSRadix Paeoniae Alba, radix Angelica sinensis, rhizoma Chuanxiong, Poria cocos, rhizoma Atractylodis macrocephala,and Alismatis rhizomeType 1 diabetic animal study (STZ induced rats)Decreasing FBG and attenuating AGEs expression in diabetic glomeruliThrough modulating oxidative stress via AGEs expression [25]

FXSTSanQi, DanShen, XuanShen, and HuangQiType 2 diabetic animal study (HFD + STZ induced rats)Preventing glomerular hypertrophy and mesangial matrix expansionThrough regulating oxidative stress [26]

HJGRehmanniae radix, Corni fructus, Dioscorea rhizome, Hoelen, Alismatis rhizome, Moutan cortex, Cinnamomi cortex, and Aconiti tuberType 1 diabetic animal study (STZ + nephrectomized rat)Reducing blood glucose and urinary protein excretion and increasing creatinine clearance, ameliorating oxidative stress and AGEs formation associated with DN, and preventing the development of renal lesions including glomerular sclerosis, tubulointerstitial lesions, mesangial expansions, and atherosclerosisInhibiting AGEs formation and sorbitol levels in kidney [27]
Type 1 diabetic animal study (WBN/Kob rats) Preventing diabetic kidney damageReducing renal oxidative injury and expression of FN/TGF-β1 proteins [28, 29]

HLBWTrigonella foenum-graecum L. (TFG) and Psoralea corylifolia L. (PC)Type 2 diabetic animal study (HFD + STZ induced rats)Improving hyperglycemia, hyperlipidemia, and proteinuriaThrough attenuating renal oxidative stress via PKC-α/NADPH oxidative pathway [31]

LDPRehmannia glutinosa, Cornel (manufactured), Moutancortex, Yam, Poria cocos, and Alisma Human study (DN patients)Improving symptoms and signs of DN, inhibiting EAR activity, lowering UAER levels, β2-microglobulin in blood, and urine, and relieving DN [32, 33]

OryeongsanPoria, Alismatis rhizoma, Polyporus umbellatus (Pers.) Fries, rhizoma Atractylodis macrocephala, and Ramulus Cinnamomi CassiaeType 1 diabetic animal study (STZ induced rats)Decreasing plasma glucose, UAER, and Ccr, attenuating mesangial matrix expansion, and downregulating increased NF-κB, TGF-β1 expression, elevated AGEs, and FN accumulation Through attenuating increased NF-κB and TGF-β1 expression [34]
Type 2 diabetic animal study (db/db mice)Decreasing TC and TG, improving blood glucose, insulin, glucose tolerance, and HOMA-IR, Ccr, urine albumin, and BUN, and reducing TGF-β1, Smad2/4, collagen IV, CTGF, and TIMPThrough disturbing the TGF-β1/Smads pathway [35]

QJCRadix astragali, Hirudo, Rehmannia root, and rhizoma PolygonatiHuman study (DN patients)Decreasing SBP and DBS, increasing ALB, and slowing down the increase of Scr and decrease of eGFR [36]

QWGRadix astragali, radix Rehmanniae, Euonymus  alatus, and RhubarbType 2 diabetic animal study (KK-Ay mice)Alleviate renal pathological changes and decreasing TGF-β1 expressionThrough inhibiting TGF-β1 expression [37]

SKWRadix astragali, Herba LeonuriType 1 diabetic animal study (STZ induced rats) Protecting renal function Through increasing NO and decreasing TGF-β1 excretion; affecting podocytes special proteins expression [38]
Type 1 diabetic animal study (STZ induced rats) Alleviating morphological damage of kidney Through reducing Ang II in plasma and kidney and inhibiting renal AT()R [39]
Cellular study (mesangial cells)Suppressing FN secretion Through TGF-β1 way [38]

SQABCRadix astragali and Salvia miltiorrhiza Type 1 diabetic animal study (STZ induced rats)Reducing 24 h UP excretion and improving reabsorption functionThrough enhancing antioxidative activity and upregulating megalin [40, 41]
Cellular study (NRK-52E cells)Protecting HG injured NRK-52E cells and improving protein uptake

TSFAstragalus, raw Rehmannia root, sanchi root, euonymus branchlet, rhubarb, bitter orange, anddogwood fruitHuman study (DN patients)Regulating and improving phospholipids metabolism
Decreasing in vivo Cys, Hcy, SAM, and SAH
Through inhibiting PKC pathway and reducing phospholipids metabolism; improving in vivo hypomethylation and oxidative stress [42, 43]
Type 2 diabetic animal study (db/db mice)Upregulating JAK1, JAK2, and STAT3 and downregulating STAT4 Regulating the JAK/STAT/SOCS pathway [44]

TSLRadix astragali, radix Rehmannia, leech, bile south star, Artemisia anomala, and Ze lanType 1 diabetic animal study (STZ + nephrectomized rat)Decreasing ECM componentsThrough downregulating TGF-β1 and TIMP-2 and upregulating MMP-2 expression [45]

TXLScorpion, leech, Centipede, groundbeetle, Cicada, Borneol, radix paeoniae rubra, and ginseng Human study (DN patients)Improving renal function, repairing the renal tubular interstitial damage, and delaying the progression of DNThrough reducing plasma ET-1 and UAER [46]
Cellular study (HKCs)Lowering miRNA-21 expression in tissue, serum, and cells, increasing E-cadherin and decreasing α-SMA expression, and decreasing collagen IV and FN and increasing Ccr Through regulating miRNA-21-induced EMT [47]
Type 2 diabetic animal study (KK-Ay mice)Reducing TGF-β1 and Smad3 expressions, restoring Smad7, decreasing collagen IV, FN,and 24 h UAER, BUN, and increasing Ccr

XCHTRadixbupleuri, Scutellaria baicalensis Georgi radix, Panax ginseng, Pinellia ternata tuber, Glycyrrhiza glabra, Ginger slice, and Zizyphus vulgaris Lam.  fructus Type 1 diabetic animal study (STZ induced rats)
Cellular study (mesangial cells)
Decreasing the expression of TGF-β1, FN, and collagen IV and increasing BMP-7 expressionThrough decreasing oxidative stress and productions of TGF-β1, FN, and collagen IV [48]

XKGRadix astragali, Mountain Cornus, leech, and winged euonymus twigType 1 diabetic animal study (STZ + nephrectomized rat)Decreasing fasting blood pressure and urinary protein in 24 hrsThrough downregulating TGF-β1 expression [49, 50]
Cellular study (mesangial cells)Inhibiting high glucose induced RMC proliferation

XXDRadix et rhizoma rhei, rhizoma coptidis, and radix Scutellaria Type 2 animal studies (HFD + STZ induced rats, db/db mice)Attenuating albuminuria and renal pathological changes, reducing AGEs, and inhibiting RAGE and inflammation factors expressionThrough downregulating NF-κB pathway and reducing renal AGEs and RAGE [51, 52]

XZTRadix astragali, radix Rehmannia, fructus ligustri lucidi, Scutellaria baicalensis Georgi, rhizoma coptidis, dodder weed, fairy spleen, and Salvia miltiorrhiza Type 1 diabetic animal study (STZ induced rats)Decreasing blood glucose and HbA1C, improving renal function, ameliorating proteinuria, and reducing glomerular extracellular matrix expansionThrough inhibiting AGEs accumulation and RAGE mRNA levels renal cortex [53]

ZDPRhizoma anemarrhenae, cortex phellodendri, radix Rehmannia preparata, rhizoma dioscorea, fructus corni, Moutan cortex, Alismatis rhizoma, and Poria Type 1 diabetic animal study (STZ induced rats)Ameliorating DNThrough inhibiting glucose and lipid metabolism and enhancing methylamine metabolism [54]

ZHMSargassum and rhizoma rheiCellular study (human mesangial cells)Preventing the process of DNThrough decreasing TGF-β1 and collagen IV expression [55]

ZQRfructus ligustri lucidi, eclipta Prostrata, and Dioscorea opposita Type 2 diabetic animal study (HFD + STZ induced rats)Inhibiting TGF-β1 and FN overexpression in the renal cortexThrough inhibiting SREBP-1c overexpression and its target [17]

ZSTLRaw Astragalus, Angelica, safflower, zedoary turmeric, dodder, radix Rehmannia, dogwood, Poria, Epimedium, earthworm, and Schisandra Human study (DN patients)Improving HbA1c and FBG, TC, TG, UAER, Scr, ANP, ET-1, and VEGF Through modifying ANP, ET-1, and VEGF [56]