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      Clinical efficacies, underlying mechanisms and molecular targets of Chinese medicines for diabetic nephropathy treatment and management

      review-article
      , , , ,   ,
      Acta Pharmaceutica Sinica. B
      Elsevier
      Chinese medicine, Herbal medicine, Diabetic nephropathy, Diabetic kidney disease, Signaling pathway, Molecular target, α-SMA, α smooth muscle actin, ACEI, angiotensin-converting enzyme inhibitor, ADE, adverse event, AGEs, advanced glycation end-products, ATK, protein kinase B, AM, mesangial area, AMPKα, adenosine monophosphate-activated protein kinase α, ARB, angiotensin receptor blocker, AREs, antioxidant response elements, BAX, BCL-2-associated X protein, BCL-2, B-cell lymphoma 2, BCL-XL, B-cell lymphoma-extra large, BMP-7, bone morphogenetic protein-7, BUN, blood urea nitrogen, BW, body weight, C, control group, cAMP, cyclic adenosine monophosphate, CCR, creatinine clearance rate, CD2AP, CD2-associated protein, CHOP, C/EBP homologous protein, CI, confidence interval, COL-I/IV, collagen I/IV, CRP, C-reactive protein, CTGF, connective tissue growth factor, D, duration, DAG, diacylglycerol, DG, glomerular diameter, DKD, diabetic kidney disease, DM, diabetes mellitus, DN, diabetic nephropathy, eGFR, estimated GFR, eIF2α, eukaryotic initiation factor 2α, EMT, epithelial-to-mesenchymal transition, EP, E-prostanoid receptor, ER, endoplasmic reticulum, ESRD, end-stage renal disease, ET-1, endothelin-1, ETAR, endothelium A receptor, FBG, fasting blood glucose, FN, fibronectin, Gαq, Gq protein alpha subunit, GCK, glucokinase, GCLC, glutamate-cysteine ligase catalytic subunit, GFR, glomerular filtration rate, GLUT4, glucose transporter type 4, GPX, glutathione peroxidase, GRB 10, growth factor receptor-bound protein 10, GRP78, glucose-regulated protein 78, GSK-3, glycogen synthase kinase 3, HbA1c, glycosylated hemoglobin, HDL-C, high density lipoprotein-cholesterol, HO-1, heme oxygenase-1, ICAM-1, intercellular adhesion molecule-1, IGF-1, insulin-like growth factor 1, IGF-1R, insulin-like growth factor 1 receptor, IκB-α, inhibitory protein α, IKK-β, IκB kinase β, IL-1β/6, interleukin 1β/6, IR, insulin receptor, IRE-1α, inositol-requiring enzyme-1α, IRS, insulin receptor substrate, JAK, Janus kinase, JNK, c-Jun N-terminal kinase, LC3, microtubule-associated protein light chain 3, LDL, low-density lipoprotein, LDL-C, low density lipoprotein-cholesterol, LOX1, lectin-like oxidized LDL receptor 1, MAPK, mitogen-activated protein kinase, MCP-1, monocyte chemotactic protein-1, MD, mean difference, MDA, malondialdehyde, MMP-2, matrix metallopeptidase 2, mTOR, mammalian target of rapamycin, MYD88, myeloid differentiation primary response 88, N/A, not applicable, N/O, not observed, NOX-4, nicotinamide adenine dinucleotide phosphate-oxidase-4, NQO1, NAD(P)H:quinone oxidoreductase 1, N/R, not reported, NRF2, nuclear factor erythroid 2-related factor 2, NF-κB, nuclear factor kappa-light-chain-enhancer of activated B cells, OCP, oxidative carbonyl protein, ORP150, 150-kDa oxygen-regulated protein, p62, sequestosome 1 protein, P70S6K, 70-kDa ribosomal protein S6 kinase, PAI-1, plasminogen activator inhibitor-1, PARP, poly(ADP-Ribose) polymerase, PBG, postprandial blood glucose, PERK, protein kinase RNA-like eukaryotic initiation factor 2A kinase, PGC-1α, peroxisome proliferator-activated receptor gamma coactivator 1α, PGE2, prostaglandin E2, PI3K, phosphatidylinositol 3 kinases, PINK1, PTEN-induced putative kinase 1, p-IRS1, phospho-IRS1, PKC, protein kinase C, PTEN, phosphatase and tensin homolog, RAGE, receptors of AGE, RASI, renin-angiotensin system inhibitor, RCT, randomized clinical trial, ROS, reactive oxygen species, SCr, serum creatinine, SD, standard deviation, SD-rat, Sprague–Dawley rat, SIRT1, sirtuin 1, SMAD, small mothers against decapentaplegic, SMD, standard mean difference, SMURF-2, SMAD ubiquitination regulatory factor 2, SOCS, suppressor of cytokine signaling proteins, SOD, superoxide dismutase, STAT, signal transducers and activators of transcription, STZ, streptozotocin, T, treatment group, TBARS, thiobarbituric acid-reactive substance, TC, total cholesterol, TCM, traditional Chinese medicine, TFEB, transcription factor EB, TG, triglyceride, TGBM, thickness of glomerular basement membrane, TGF-β, tumor growth factor β, TGFβR-I/II, TGF-β receptor I/II, TII, tubulointerstitial injury index, TLR-2/4, toll-like receptor 2/4, TNF-α, tumor necrosis factor α, TRAF5, tumor-necrosis factor receptor-associated factor 5, UACR, urinary albumin to creatinine ratio, UAER, urinary albumin excretion rate, UMA, urinary microalbumin, UP, urinary protein, VCAM-1, vascular cell adhesion molecule-1, VEGF, vascular endothelial growth factor, WMD, weight mean difference, XBP-1, spliced X box-binding protein 1

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          Abstract

          Diabetic nephropathy (DN) has been recognized as a severe complication of diabetes mellitus and a dominant pathogeny of end-stage kidney disease, which causes serious health problems and great financial burden to human society worldwide. Conventional strategies, such as renin-angiotensin-aldosterone system blockade, blood glucose level control, and bodyweight reduction, may not achieve satisfactory outcomes in many clinical practices for DN management. Notably, due to the multi-target function, Chinese medicine possesses promising clinical benefits as primary or alternative therapies for DN treatment. Increasing studies have emphasized identifying bioactive compounds and molecular mechanisms of reno-protective effects of Chinese medicines. Signaling pathways involved in glucose/lipid metabolism regulation, antioxidation, anti-inflammation, anti-fibrosis, and podocyte protection have been identified as crucial mechanisms of action. Herein, we summarize the clinical efficacies of Chinese medicines and their bioactive components in treating and managing DN after reviewing the results demonstrated in clinical trials, systematic reviews, and meta-analyses, with a thorough discussion on the relative underlying mechanisms and molecular targets reported in animal and cellular experiments. We aim to provide comprehensive insights into the protective effects of Chinese medicines against DN.

          Graphical abstract

          Diabetic nephropathy is one of the most severe complications of diabetes mellitus. Chinese medicines have been intensively studied in treating diabetic nephropathy. This review comprehensively summarizes and discusses the clinical efficacies and underlying mechanisms of Chinese medicines for diabetic nephropathy, providing deep insights and profound perspectives into this field.

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          Most cited references152

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          Diabetic kidney disease

          The kidney is arguably the most important target of microvascular damage in diabetes. A substantial proportion of individuals with diabetes will develop kidney disease owing to their disease and/or other co-morbidity, including hypertension and ageing-related nephron loss. The presence and severity of chronic kidney disease (CKD) identify individuals who are at increased risk of adverse health outcomes and premature mortality. Consequently, preventing and managing CKD in patients with diabetes is now a key aim of their overall management. Intensive management of patients with diabetes includes controlling blood glucose levels and blood pressure as well as blockade of the renin-angiotensin-aldosterone system; these approaches will reduce the incidence of diabetic kidney disease and slow its progression. Indeed, the major decline in the incidence of diabetic kidney disease (DKD) over the past 30 years and improved patient prognosis are largely attributable to improved diabetes care. However, there remains an unmet need for innovative treatment strategies to prevent, arrest, treat and reverse DKD. In this Primer, we summarize what is now known about the molecular pathogenesis of CKD in patients with diabetes and the key pathways and targets implicated in its progression. In addition, we discuss the current evidence for the prevention and management of DKD as well as the many controversies. Finally, we explore the opportunities to develop new interventions through urgently needed investment in dedicated and focused research. For an illustrated summary of this Primer, visit: http://go.nature.com/NKHDzg.
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            CKD in diabetes: diabetic kidney disease versus nondiabetic kidney disease

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              • Article: not found

              Epigenetics and epigenomics in diabetic kidney disease and metabolic memory

              The development and progression of diabetic kidney disease (DKD), a highly prevalent complication of diabetes mellitus, is influenced by both genetic and environmental factors. DKD is an important contributor to the morbidity of patients with diabetes mellitus, indicating a clear need for an improved understanding of disease aetiology to inform the development of more efficacious treatments. DKD is characterized by an accumulation of extracellular matrix, hypertrophy, and fibrosis in kidney glomerular and tubular cells. Increasing evidence shows that genes associated with these features of DKD are regulated not only by classical signalling pathways, but also by epigenetic mechanisms, involving chromatin histone modifications, DNA methylation, and non-coding RNAs. These mechanisms can respond to changes in the environment and importantly, might mediate the persistent long-term expression of DKD-related genes and phenotypes induced by prior glycaemic exposure, despite subsequent glycaemic control, a phenomenon called metabolic memory. Detection of epigenetic events during the early stages of DKD could be valuable for timely diagnosis and prompt treatment to prevent progression to end-stage renal disease. Identification of epigenetic signatures of DKD via epigenome-wide association studies might also inform precision medicine approaches. Here, we highlight the emerging role of epigenetics and epigenomics in DKD, and the translational potential of candidate epigenetic factors and non-coding RNAs as biomarkers and drug targets for DKD.
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                Author and article information

                Contributors
                Journal
                Acta Pharm Sin B
                Acta Pharm Sin B
                Acta Pharmaceutica Sinica. B
                Elsevier
                2211-3835
                2211-3843
                02 February 2021
                September 2021
                02 February 2021
                : 11
                : 9
                : 2749-2767
                Affiliations
                [1]School of Chinese Medicine, Li Ka Shing Faculty of Medicine, the University of Hong Kong, Hong Kong SAR 999077, China
                Author notes
                []Corresponding author. yfeng@ 123456hku.hk
                Article
                S2211-3835(21)00002-2
                10.1016/j.apsb.2020.12.020
                8463270
                34589395
                6cde21cc-9dfe-499c-a049-2394fc4e6c5e
                © 2021 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 17 August 2020
                : 17 October 2020
                : 25 December 2020
                Categories
                Review

                chinese medicine,herbal medicine,diabetic nephropathy,diabetic kidney disease,signaling pathway,molecular target,α-sma, α smooth muscle actin,acei, angiotensin-converting enzyme inhibitor,ade, adverse event,ages, advanced glycation end-products,atk, protein kinase b,am, mesangial area,ampkα, adenosine monophosphate-activated protein kinase α,arb, angiotensin receptor blocker,ares, antioxidant response elements,bax, bcl-2-associated x protein,bcl-2, b-cell lymphoma 2,bcl-xl, b-cell lymphoma-extra large,bmp-7, bone morphogenetic protein-7,bun, blood urea nitrogen,bw, body weight,c, control group,camp, cyclic adenosine monophosphate,ccr, creatinine clearance rate,cd2ap, cd2-associated protein,chop, c/ebp homologous protein,ci, confidence interval,col-i/iv, collagen i/iv,crp, c-reactive protein,ctgf, connective tissue growth factor,d, duration,dag, diacylglycerol,dg, glomerular diameter,dkd, diabetic kidney disease,dm, diabetes mellitus,dn, diabetic nephropathy,egfr, estimated gfr,eif2α, eukaryotic initiation factor 2α,emt, epithelial-to-mesenchymal transition,ep, e-prostanoid receptor,er, endoplasmic reticulum,esrd, end-stage renal disease,et-1, endothelin-1,etar, endothelium a receptor,fbg, fasting blood glucose,fn, fibronectin,gαq, gq protein alpha subunit,gck, glucokinase,gclc, glutamate-cysteine ligase catalytic subunit,gfr, glomerular filtration rate,glut4, glucose transporter type 4,gpx, glutathione peroxidase,grb 10, growth factor receptor-bound protein 10,grp78, glucose-regulated protein 78,gsk-3, glycogen synthase kinase 3,hba1c, glycosylated hemoglobin,hdl-c, high density lipoprotein-cholesterol,ho-1, heme oxygenase-1,icam-1, intercellular adhesion molecule-1,igf-1, insulin-like growth factor 1,igf-1r, insulin-like growth factor 1 receptor,iκb-α, inhibitory protein α,ikk-β, iκb kinase β,il-1β/6, interleukin 1β/6,ir, insulin receptor,ire-1α, inositol-requiring enzyme-1α,irs, insulin receptor substrate,jak, janus kinase,jnk, c-jun n-terminal kinase,lc3, microtubule-associated protein light chain 3,ldl, low-density lipoprotein,ldl-c, low density lipoprotein-cholesterol,lox1, lectin-like oxidized ldl receptor 1,mapk, mitogen-activated protein kinase,mcp-1, monocyte chemotactic protein-1,md, mean difference,mda, malondialdehyde,mmp-2, matrix metallopeptidase 2,mtor, mammalian target of rapamycin,myd88, myeloid differentiation primary response 88,n/a, not applicable,n/o, not observed,nox-4, nicotinamide adenine dinucleotide phosphate-oxidase-4,nqo1, nad(p)h:quinone oxidoreductase 1,n/r, not reported,nrf2, nuclear factor erythroid 2-related factor 2,nf-κb, nuclear factor kappa-light-chain-enhancer of activated b cells,ocp, oxidative carbonyl protein,orp150, 150-kda oxygen-regulated protein,p62, sequestosome 1 protein,p70s6k, 70-kda ribosomal protein s6 kinase,pai-1, plasminogen activator inhibitor-1,parp, poly(adp-ribose) polymerase,pbg, postprandial blood glucose,perk, protein kinase rna-like eukaryotic initiation factor 2a kinase,pgc-1α, peroxisome proliferator-activated receptor gamma coactivator 1α,pge2, prostaglandin e2,pi3k, phosphatidylinositol 3 kinases,pink1, pten-induced putative kinase 1,p-irs1, phospho-irs1,pkc, protein kinase c,pten, phosphatase and tensin homolog,rage, receptors of age,rasi, renin-angiotensin system inhibitor,rct, randomized clinical trial,ros, reactive oxygen species,scr, serum creatinine,sd, standard deviation,sd-rat, sprague–dawley rat,sirt1, sirtuin 1,smad, small mothers against decapentaplegic,smd, standard mean difference,smurf-2, smad ubiquitination regulatory factor 2,socs, suppressor of cytokine signaling proteins,sod, superoxide dismutase,stat, signal transducers and activators of transcription,stz, streptozotocin,t, treatment group,tbars, thiobarbituric acid-reactive substance,tc, total cholesterol,tcm, traditional chinese medicine,tfeb, transcription factor eb,tg, triglyceride,tgbm, thickness of glomerular basement membrane,tgf-β, tumor growth factor β,tgfβr-i/ii, tgf-β receptor i/ii,tii, tubulointerstitial injury index,tlr-2/4, toll-like receptor 2/4,tnf-α, tumor necrosis factor α,traf5, tumor-necrosis factor receptor-associated factor 5,uacr, urinary albumin to creatinine ratio,uaer, urinary albumin excretion rate,uma, urinary microalbumin,up, urinary protein,vcam-1, vascular cell adhesion molecule-1,vegf, vascular endothelial growth factor,wmd, weight mean difference,xbp-1, spliced x box-binding protein 1
                chinese medicine, herbal medicine, diabetic nephropathy, diabetic kidney disease, signaling pathway, molecular target, α-sma, α smooth muscle actin, acei, angiotensin-converting enzyme inhibitor, ade, adverse event, ages, advanced glycation end-products, atk, protein kinase b, am, mesangial area, ampkα, adenosine monophosphate-activated protein kinase α, arb, angiotensin receptor blocker, ares, antioxidant response elements, bax, bcl-2-associated x protein, bcl-2, b-cell lymphoma 2, bcl-xl, b-cell lymphoma-extra large, bmp-7, bone morphogenetic protein-7, bun, blood urea nitrogen, bw, body weight, c, control group, camp, cyclic adenosine monophosphate, ccr, creatinine clearance rate, cd2ap, cd2-associated protein, chop, c/ebp homologous protein, ci, confidence interval, col-i/iv, collagen i/iv, crp, c-reactive protein, ctgf, connective tissue growth factor, d, duration, dag, diacylglycerol, dg, glomerular diameter, dkd, diabetic kidney disease, dm, diabetes mellitus, dn, diabetic nephropathy, egfr, estimated gfr, eif2α, eukaryotic initiation factor 2α, emt, epithelial-to-mesenchymal transition, ep, e-prostanoid receptor, er, endoplasmic reticulum, esrd, end-stage renal disease, et-1, endothelin-1, etar, endothelium a receptor, fbg, fasting blood glucose, fn, fibronectin, gαq, gq protein alpha subunit, gck, glucokinase, gclc, glutamate-cysteine ligase catalytic subunit, gfr, glomerular filtration rate, glut4, glucose transporter type 4, gpx, glutathione peroxidase, grb 10, growth factor receptor-bound protein 10, grp78, glucose-regulated protein 78, gsk-3, glycogen synthase kinase 3, hba1c, glycosylated hemoglobin, hdl-c, high density lipoprotein-cholesterol, ho-1, heme oxygenase-1, icam-1, intercellular adhesion molecule-1, igf-1, insulin-like growth factor 1, igf-1r, insulin-like growth factor 1 receptor, iκb-α, inhibitory protein α, ikk-β, iκb kinase β, il-1β/6, interleukin 1β/6, ir, insulin receptor, ire-1α, inositol-requiring enzyme-1α, irs, insulin receptor substrate, jak, janus kinase, jnk, c-jun n-terminal kinase, lc3, microtubule-associated protein light chain 3, ldl, low-density lipoprotein, ldl-c, low density lipoprotein-cholesterol, lox1, lectin-like oxidized ldl receptor 1, mapk, mitogen-activated protein kinase, mcp-1, monocyte chemotactic protein-1, md, mean difference, mda, malondialdehyde, mmp-2, matrix metallopeptidase 2, mtor, mammalian target of rapamycin, myd88, myeloid differentiation primary response 88, n/a, not applicable, n/o, not observed, nox-4, nicotinamide adenine dinucleotide phosphate-oxidase-4, nqo1, nad(p)h:quinone oxidoreductase 1, n/r, not reported, nrf2, nuclear factor erythroid 2-related factor 2, nf-κb, nuclear factor kappa-light-chain-enhancer of activated b cells, ocp, oxidative carbonyl protein, orp150, 150-kda oxygen-regulated protein, p62, sequestosome 1 protein, p70s6k, 70-kda ribosomal protein s6 kinase, pai-1, plasminogen activator inhibitor-1, parp, poly(adp-ribose) polymerase, pbg, postprandial blood glucose, perk, protein kinase rna-like eukaryotic initiation factor 2a kinase, pgc-1α, peroxisome proliferator-activated receptor gamma coactivator 1α, pge2, prostaglandin e2, pi3k, phosphatidylinositol 3 kinases, pink1, pten-induced putative kinase 1, p-irs1, phospho-irs1, pkc, protein kinase c, pten, phosphatase and tensin homolog, rage, receptors of age, rasi, renin-angiotensin system inhibitor, rct, randomized clinical trial, ros, reactive oxygen species, scr, serum creatinine, sd, standard deviation, sd-rat, sprague–dawley rat, sirt1, sirtuin 1, smad, small mothers against decapentaplegic, smd, standard mean difference, smurf-2, smad ubiquitination regulatory factor 2, socs, suppressor of cytokine signaling proteins, sod, superoxide dismutase, stat, signal transducers and activators of transcription, stz, streptozotocin, t, treatment group, tbars, thiobarbituric acid-reactive substance, tc, total cholesterol, tcm, traditional chinese medicine, tfeb, transcription factor eb, tg, triglyceride, tgbm, thickness of glomerular basement membrane, tgf-β, tumor growth factor β, tgfβr-i/ii, tgf-β receptor i/ii, tii, tubulointerstitial injury index, tlr-2/4, toll-like receptor 2/4, tnf-α, tumor necrosis factor α, traf5, tumor-necrosis factor receptor-associated factor 5, uacr, urinary albumin to creatinine ratio, uaer, urinary albumin excretion rate, uma, urinary microalbumin, up, urinary protein, vcam-1, vascular cell adhesion molecule-1, vegf, vascular endothelial growth factor, wmd, weight mean difference, xbp-1, spliced x box-binding protein 1

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