Curcumin Reinforces MiR-29a Expression, Reducing Mesangial Fibrosis in a Model of Diabetic Fibrotic Kidney via Modulation of CB1R Signaling

Abstract

Renal fibrosis is a hallmark event in the pathogenesis of diabetic nephropathy. Considerable evidence now supports that multiple intracellular signaling pathways are critically involved in renal fibrosis. Previously, our studies have shown that dysregulation of the MicroRNA 29a (miR-29a)- or cannabinoid type 1 receptor (CB1R)-mediated signaling cascade in renal glomeruli substantially contributes to diabetic renal fibrosis. The purpose of the current study was to explore whether curcumin, a natural polyphenolic compound with potential renoprotective activity, could modulate the miR-29a/CB1R signaling axis to attenuate renal fibrosis. In this study, rat renal mesangial cells cultured in high glucose (HG) and the diabetic db/db mice were used as an in vitro and in vivo model of diabetes, respectively. Our results showed that in rat renal mesangial cells, curcumin treatment substantially counteracted HG-induced changes in the expressions of miR-29a, CB1R, peroxisome proliferator-activated receptor gamma (PPAR-γ), and a profibrotic marker type IV collagen (collagen IV), as assessed by quantitative Real-Time Polymerase chain reaction (RT-PCR). Furthermore, in the db/db mouse model, administration of curcumin markedly lowered urinary albumin excretion, and reduced deposition of extracellular matrices including collagen IV in renal tissues. Importantly, quantitative RT-PCR, in situ hybridization, and immunohistochemical analysis revealed that curcumin treatment consistently blocked diabetes-induced downregulation of miR-29a and upregulation of CB1R in renal glomeruli. Collectively, our study provides novel evidence showing that curcumin can rescue the dysregulated miR-29a/CB1R signaling pathway in glomerular mesangium to ameliorate diabetic renal fibrosis.

1. Introduction

Diabetic nephropathy, one of the complications of diabetes mellitus, is now the leading cause of end-stage renal disease throughout the world [1]. In diabetic nephropathy, renal fibrosis is the most prominent histological feature [2]. Renal fibrosis is characterized by excessive accumulation of extracellular matrix (ECM) proteins in the glomerular mesangium and in tubulointerstitium, which causes thickening of the glomerular and tubular basement membranes, mesangial expansion, and tubulointerstitial fibrosis [3,4]. Particularly, with the progression of glomerular basement membrane thickening and mesangial expansion, glomerular capillaries are gradually occluded and the patency of capillary lumens is then decreased, which ultimately lead to renal failure [5].

It is believed that the development of renal fibrosis is a complicated biological process, which may involve numerous functionally distinct intracellular signaling pathways [6]. Several studies have implicated that the type 1 cannabinoid receptor (CB1R)-mediated signaling participates in promoting fibrosis and inflammation of renal tissue [7,8,9,10,11]. CB1R is a Gi/o protein-coupled receptor that has been reported to mediate various pathophysiological processes including adipogenesis [12], bone remodeling [13], neurite outgrowth [14], and liver fibrosis [15]. In our earlier studies, we also observed that CB1R expression was significantly upregulated in streptozotocin (STZ)-induced diabetic rats, and gain of CB1R function in animal models sufficiently contributed to intense renal fibrosis and inflammation [16]. Our studies further elucidated that the induction of renal fibrosis and inflammation by CB1R signaling was closely associated with decreased expression of peroxisome proliferator-activated receptor gamma (PPAR-γ), a nuclear hormone receptor [16]. Noteworthily, it is generally recognized that activation of PPAR-γ signaling could exert renoprotective effects in different nondiabetic or diabetic animal models [17,18,19,20].

MicroRNAs are short non-coding RNAs that act to silence gene expression via mRNA degradation or translation repression. Notably, a large amount of evidence has shown that microRNAs are involved in various kidney diseases including diabetic nephropathy [21,22]. We previously have showed that decreased miR-29a consistently occurred in high glucose (HG)-treated mouse mesangial cells and in renal glomeruli of STZ-induced diabetic mice [23,24]. In particular, gain of miR-29a function in HG-cultured mesangial cells or in the diabetic mouse model could substantially attenuate renal fibrogenesis [24]. More recently, we found that ectopic expression of miR-29a could downregulate the detrimental CB1R signaling, consequently leading to the restoration of PPAR-γ expression and the amelioration of renal fibrosis in STZ-treated mice [25]. Although the precise molecular mechanism underlying the action of miR-29a in renal injury is still not fully understood, miR-29a may serve as a negative regulator of CB1R signaling, and act to directly or indirectly prevent the expression of proinflammatory and profibrotic genes in renal tissues.

Curcumin, a bioactivepolyphenolic compound derived from the roots of turmeric (Curcuma longa L.), has exhibited antioxidant, anti-inflammation, anticancer, and antifibrotic activities [26,27]. Many studies exhibited that administration of curcumin could help to improve non-diabetic or diabetic renal diseases by alleviating renal inflammation and fibrosis [28]. Curcumin has been demonstrated to influence the expression or activity of several pro-inflammatory molecules such as Nuclear factor-kapa-light-chain-enhancer of activated B cells (NF-κB) [29], Tumor Necrosis Factor-α (TNF-α) [30], caveolin-1 [31], and Interleukin-1β (IL-1β) [32]. Moreover, it has also been shown that under diabetic conditions, curcumin could retard the progression of renal fibrosis by targeting several specific signaling pathways associated with fibrogenesis [28,33]. Although curcumin has been shown to have potent antifibrotic activities, the detailed mechanism of action of curcumin in suppressing diabetic renal fibrosis has not yet been fully elucidated. Herein, we aimed to explore whether curcumin has any effects on the regulation of the miR-29a/CB1R/PPAR-γ signaling axis to prevent renal fibrosis in diabetic mice.

2. Materials and Methods

2.1. Cell Culture Conditions

Rat mesangialcells (ATCC; Manassas, VA, USA #CRL-2573) were maintained in Dulbecco’s modified eagle (DME) medium containing 10% fetal bovine serum at 37 °C with 5% Carbon dioxide. Cells cultured at 5.5 mM D-glucose served as the normal control group. For the high-glucose culture, cells at a density of 1×10⁶ cells per well (6-well plates) were grown in DME medium containing 35 mM D-glucosefor 48 h as described previously [34]. Curcumin powder, derived from Curcuma longa,was purchased from Sigma-Aldrich (catalog #C1386). Curcumin was dissolved in dimethyl sulfoxide (DMSO; #D2438; Sigma-Aldrich, USA)to obtain a concentration of 10 or 50 mM, and then stored in the dark at −20 °C. All dilutions of curcumin were made in DME medium and the final concentration of DMSO was 0.1% in all experiments of cell treatment. For cell viability analysis, mesangial cells(1 × 10⁵ cells per well) were seeded in 96-well plates and treated with normal glucose (5.5 mM D-glucose), high glucose (35 mM D-glucose), or high glucose supplemented withvarious concentrations of curcumin. After 48 h of treatment exposure, The Cell Proliferation Kit (XTT assay) (Roche) was used to measure cell viability according to the manufacturer’s instructions.

2.2. Quantitative Reverse-Transcription (RT)- Polymerase Chain Reaction (PCR)

Total RNA isolation from cells (or tissues), reverse transcription of cellular RNA (Ribonucleic acid), and quantitative PCR analysis were performed as mentioned previously [35]. In brief, total RNAs extracted from cells (or tissues) were reverse-transcribed using the High-Capacity cDNA Reverse Transcription Kits (ThermoFisher Scientific, Lithuania), and the resultant complementary DNAs served as templates for quantitative PCR using the custom TaqMan® Gene Expression Assay Kits (ThermoFisher Scientific, USA) and the ABI 7300 Fast Real-Time PCR System (Applied Biosystems). The change in gene expression was calculated as 2^−ΔΔCt, where ΔΔCt = ΔCt(treatment) − ΔCt(control) and ΔCt = Ct(target) − Ct(β-actin).

2.3. In Vivo Animal Model

A total of 12 6-week-old db/db mice (C57BLKS/J Iar-+Lepr^db/+Lepr^db; Jackson Laboratory) were randomly divided into 2 groups. Curcumin (#C1386; Sigma-Aldrich) was dissolved in 50% DMSO (v/v with Phosphate Buffered Saline). Each group of the db/db mice received intraperitoneal injections of 10 mg curcumin/kg body weight (n = 6) or 50% DMSO/PBS (n = 6) for eight weeks (five times a week). Six age-matched db/m mice were used as the normal control group. Mice were sacrificed with an overdose of pentobarbital sodium, and then kidneys were immediately removed and weighed. The protocols of animal experiments were certified by the Institutional Animal Care and Use Committee of the Chang Gung Memorial Hospital (No. 2019091604) and were conducted following the guideline of National Institutes of Health (Bethesda, MD) and the Animal Protection Law by the Council of Agriculture (Taiwan).

2.4. Measurement of Glycated Hemoglobulin( HbA1c) Levels and Urine Albumin Excretion

After 8-week treatment, serum levels of HbA1c were measured using the assay kit (Primus Diagnostics, Kansas, MO, USA) following the manufacturer’s protocol. The twenty-four-hours urine samples were collected in the metabolism cages and the levels of urinary albumin were measured by the Albumin Assay Kit (Dade Behring, Newark, NJ, USA) following the manufacturer’s instructions.

2.5. Masson’s Trichrome, Periodic Acid-Schiff (PAS), and Immunohistochemicalstaining

For assessment of collagen deposition in renal tissues, Masson’s trichrome staining was performed and evaluated as described elsewhere [36]. Mesangial matrix expansion was assessed by periodic acid-Schiff staining following the manufacturer’s procedures (Sigma-Aldrich, St Louis, MO, USA). For immunohistochemistry staining, kidneysections (5-µm thick) were immunostained with anti-collagen IV antibody (#ab6586; Abcam, USA) or anti-CB1R antibody (#BS2712; BioWorld, USA), together with the use of the immunostaining kits (BioGenex, San Ramon, CA, USA).

2.6. Quantitative Integrated Optical Density (IOD) Analysis

The areas of glomeruli from each stained section were randomly chosen and photographed (×400 magnification). The staining intensity in glomeruli was analyzed using the Image-Pro Plus software (Media Cybernetics, Silver Spring, MD, Version 6.3). For each analysis, at least 25 microscopic fields taken from a total of five sections of kidney from each mouse were quantified.

2.7. Laser Capture Microdissection (LCM) of Kidney Tissues

Kidneys were anatomized from mice, and then perfused with phosphate-buffered saline. Subsequently, kidney tissue slices were fixed with 4% formaldehyde, embedded in paraffin, and sectioned at 4-µm thick under RNase-free conditions. The glomerular compartments in the formaldehyde-fixed renal sections were isolated using the VeritasMicrodissectionInstrument (Arcturus Bioscience, Veritas703, CA, USA) as described previously [35]. We picked glomeruli tissue structures of any shape using a variety of drawing tools and trained the system to automatically target high-contrast labeled cells. Two hundred glomeruli from kidney sections of each mouse were collected for extraction of total RNA.

2.8. In Situ Hybridization

Paraffin-embedded renal sections (5 µm) and the digoxigenin-labeled probe for miR-29a (Exiqon Biotechnology) were used in the insituhybridization as described previously [24]. Briefly, renal sections were first deproteinized with proteinase K (10 µg/mL), incubated with a pre-hybridization solution (50% formamide, 5X saline-sodium citrate (SSC), 0.1% Tween, 50 µg/mL heparin, and 500 µg/mL yeast RNA), and then hybridized with the digoxigenin-labeled probes in a buffer (containing 0.3 M sodium chloride (NaCl), 20 mM Tris-HCl (hydrochloric acid), 0.5 mM EDTA (ethylenediaminetetraacetic acid), 10 mM NaPO4, 10% dextran sulfate, 1XDenhardt, and 0.5 mg/mL yeast RNA). The hybrid was subsequently detected with anti-digoxigenin antibody.

2.9. Statistical Analysis

All data are expressed as means ± standard errors. For in vitro studies, data were derived from more than three independent experiments. An independent-sample t-test was utilized to evaluate the difference between the control and treatment groups. A parametric analysis of variance and Bonferroni post hoc test were used to analyze differences among different groups. p < 0.05 was considered statistically significant.

3. Results

3.1. Curcumin Blocks High Glucose-Induced Changes in the Expressions of Collagen IV, CB1R, PPAR-γ, and MiR-29a in Cultured Rat Mesangial Cells

To explore the potential mechanism by which curcumin alleviates diabetic renal fibrosis, we initially evaluated the cytotoxic effects of different concentrations of curcumin on rat mesangial cells(Figure 1a). The cell viability of rat mesangial cells cultured in normal glucose (NC), high glucose (HG), or HG in combination with different concentrations (0.1, 1, 10, and 50 μM) of curcumin (HG + Cur) for 48 h were assessed by XTT assay (Figure 1a). As compared to the control HG group without curcumin, the rat mesangial cells treated with 0.1, 1.0, or 10 μM of curcumin did not show significant changes in cell viability (Figure 1a). However, treatment with curcumin at a concentration of 50 μM markedly reduced cell viability. Therefore, we used 10 μM curcumin for further experiments.

Next, rat mesangial cells were cultured in the normal medium or HG medium with or without the addition of 10 μM curcumin. At 48 h after culture, total RNAs isolated from these treated mesangial cells were used for analyzing target gene expression by quantitative RT-PCR. These specific fibrosis-related genes included collagen IV, CB1R, PPAR-γ, and miR-29a. Consistent with our previous studies [25], HG treatment significantly increased the levels of collagen IV and CB1R mRNAs (Figure 1b,c), but decreased the levels of PPAR-γ mRNA and miR-29a RNA in mesangial cells (Figure 1d,e). In particular, curcumin treatment substantially attenuated HG-mediated upregulation of collagen IV and CB1R, and downregulation of PPAR-γ and miR-29a in mesangial cells (Figure 1b–e). These results indicated that curcumin could suppress HG-induced mesangialfibrogenesis through modulating the miR-29a/CB1R/PPAR-γ signaling axis.

3.2. Curcumin Treatment Improves Urinary Albumin Excretion in Diabetic Mice

To determine whether curcumin indeed improved diabetes-induced renal dysfunction in vivo, the diabetic db/db mice were injected intraperitoneally with curcumin (10 mg/kg) five times a week and for a total of eight weeks. In comparison with the age-matched db/m (nondiabetic) mice, the db/db mice displayed substantially elevated levels of HbA1c, a common glycemic marker (Figure 2a). However, treatment of the db/db mice with curcumin (db/db + Cur) did not affect HbA1c levels (Figure 2a). Although the body and kidney weights in the db/db mice with or without curcumin treatment were much heavier than those in the control db/m mice, no significant difference was detected for the ratio of kidney weight to body weight among these groups (Figure 2b). Analysis of proteinuria showed that urinary albumin excretion in the db/db mice was about 18-fold higher than that in the db/m mice (Figure 2c). Elevated urinary albumin excretion in the db/db mice could be markedly reduced by curcumin treatment (Figure 2c). These results indicated that curcumin could remarkably improve the urinary albumin excretion in db/db mice, which was beyond blood sugar levels (HbA1c levels).

3.3. Renal Fibrosis in Diabetic Mice Is Alleviated by Curcumin

To look into the effect of curcumin on kidney fibrosis in diabetic mice, deposition of collagens in renal glomeruli was evaluated by Masson’s trichrome staining and by immunohistochemistry (IHC) with anti-collagen IV antibody. As compared to the control db/m mice, the db/db mice exhibited high degrees of collagen deposition (Masson’s trichrome staining) and intense collagen IV stain (IHC staining) in renal glomeruli (Figure 3a–c). The accumulation of collagens in diabetic renal glomeruli could be significantly attenuated by administration of curcumin (Figure 3a–c). To further confirm the expression levels of collagen IV in renal glomeruli, total RNAs extracted from renal glomeruli, which were isolated from kidney sections by laser capture microdissection, were subjected to real-time RT-PCR analysis. Results from the quantitative RT-PCR assay indeed showed that the mRNA levels of collagen IV were significantly reduced in the curcumin-treated db/db mice as compared to the untreated db/db mice (Figure 3d). Together, our results supported that curcumin treatment could attenuate renal fibrosis in the db/db mice.

3.4. Curcumin Treatment Suppresses CB1R Upregulation in Renal Glomeruli of Diabetic Mice

To further examine the effect of curcumin on glomerular matrix expansion in diabetic mice, the periodic acid-Schiff (PAS) staining that delineates mesangial matrix expansion was also performed. Notably, marked mesangial matrix expansion was observed in renal glomeruli of the db/db mice, which could be significantly attenuated by curcumin (Figure 4a,b). Since CB1R upregulation critically contributed to renal fibrosis, the expression of CB1R in renal glomeruli was also evaluated by IHC staining. Results from the IHC analysis revealed that intense CB1R stain was observed in renal glomeruli of the db/db mice as compared to the db/m mice (Figure 4a,c).Curcumin administration remarkably decreased the levels of CB1R in the db/dbmice (Figure 4a,c). Additionally, the mRNA expression of CB1R in renal glomeruli isolated using the laser-capture microdissection was also analyzed by quantitative RT-PCR (Figure 4d). Consistent with the results of IHC stains, the quantitative RT-PCR analysis also demonstrated that curcumin treatment significantly reduced the glomerular CB1R expression in the db/dbmice (Figure 4d).

3.5. Curcumin Treatment Restores Mir-29a Levels in Renal Glomeruli of Diabetic Mice

Due to the critical role of miR-29a in renal fibrosis, the expression levels of miR-29a were examined in the db/m mice and in the db/db mice with or without curcumin treatment. In situ hybridization confirmed that the expression levels of miR-29a were significantly lower in the db/db mice than in the control db/m mice (Figure 5a,b). However, curcumin treatment substantially restored the expression of miR-29a in glomeruli of the db/db mice (Figure 5a,b). These results indicated that miR-29a might be involve in curcumin-mediated restoration of kidney function in the diabetic db/db mice. To further confirm the expression of miR-29a in renal glomeruli, levels of miR-29a RNA were evaluated by quantitative RT-PCR. In the experiments, glomerular compartments were obtained by laser capture microdissection (Figure 5c), and total RNAs extracted from these samples were used to analyze the expression level of miR-29a RNA. As compared to the db/m mice, the db/db mice consistently exhibited reduced levels of the glomerular miR-29a (Figure 5d). Treatment of the db/db mice with curcumin substantially restored the glomerular miR-29a expression (Figure 5d).

4. Discussion

Our earlier studies have shown that dysregulation of the miR-29a- and CB1R-mediated signaling pathways in renal glomeruli critically contributes to diabetic renal fibrosis [16,24,25]. In this report, we confirmed that decreased expression of miR-29a and increased expression of CB1R, along with upregulation of fibrotic markers (such as collagen IV), were consistently observed in HG-cultured renal mesangial cells and in renal glomeruli of the diabetic db/db mice (summary in Figure 6). Importantly, we showed that curcumin treatment could efficiently rescue the dysregulated miR-29a/CB1R signaling axis to alleviate fibrogenesis in HG-cultured mesangial cells and in renal glomeruli of the db/db mice (Figure 6). Overall, our findings suggest that targeting the miR-29a/CB1R signaling pathway in the glomerular mesangium may be a new action mechanism of curcumin to attenuate diabetic renal fibrosis.

Curcumin has attracted great attention as a potential agent for treating renal fibrosis, mainly due to its safety, cheapness, and renoprotective efficacy [28,37,38]. According to previous studies, curcumin could resolve renal fibrosis via preventing the release of pro-inflammatory molecules (such as Monocyte Chemoattractant Protein-1 (MCP-1), TNF-α, and IL-1β), maintaining the oxidant/antioxidant balance, inhibiting myofibroblast activation, and reducing extracellular matrix accumulation [28]. Although curcumin has been demonstrated to target several specific signaling pathways (such as transforming growth factor-β/Smads, Extracellular Regulated protein Kinases, and Peroxisome Proliferator-activated Receptor-γ pathways) in various renal disease models [28], the action of curcumin in preventing glomerulosclerosis and renal fibrosis is still not yet fully understood. Due to the fact that different cell types or animal models of diabetes could potentially have differential responses to curcumin, we here tested the effect of curcumin in diabetic db/db mice, a model of type 2 diabetic mellitus, and especially focused on the structural and functional alterations of the glomerular mesangium. Consistent with previous studies using the Streptozotocin (STZ)-induced diabetic animal models, we here showed that curcumin treatment remarkably prevented fibrogenesis in renal glomeruli of the db/db mice.

Despite extensive studies, the current medications are still not enough to prevent the progression of diabetic nephropathy. The lack of effective treatment for diabetic nephropathy is partly due to the lack of detailed understanding of the molecular mechanisms underlying fibrogenesis. Although numerous intracellular signaling pathways and microRNAs that participate in diabetic renal fibrosis have been increasingly reported in various in vitro and animalmodels [6,21,39], cross-regulation of these identified signaling cascades still remains to be further explored. Previously, we revealed that miR-29a acts as a potent antifibrotic factor in renal tissues, and the action of miR-29a in preventing diabetes-induced glomerulosclerosis could be mainly attributed to downregulation of the detrimental CB1R signaling [25]. Interestingly, we additionally found that miR-29a could positively regulate the Wnt/β-catenin signaling pathway, consequently resulting in the prevention of diabetic glomerular dysfunction [24]. From the present study and previous studies, it seems likely that miR-29a plays a central role in controlling multiple fibrogenic signaling pathways. Although we have shown that curcumin could modulate the dysregulated miR-29a/CB1R/PPAR-γ signaling pathway in diabetic db/db mice, it may be important for future research to determine whether curcumin could affect the Wnt/β-catenin signaling or other known downstream signaling of miR-29a to alleviate renal fibrosis in the db/db mice.

Although miR-29a has been demonstrated as an important regulator for renal fibrosis in diabetic animals, how miR-29a expression is regulated remains poorly understood. It is possible that curcumin may function to target signaling pathways upstream of miR-29a expression to alleviate diabetic renal fibrosis. Interestingly, we here noticed that the expression level of miR-29a in mesangial cells treated with HG and 10 μM curcumin (Figure 1e, HG + Cur) was significantly higher than that in the normal control group (Figure 1e, NC). These results strongly imply that curcumin may be a potent inducer for miR-29a expression and may exert “dominant influence” over the effect of high glucose on the expression of miR-29a in cultured mesangial cells.Therefore, understanding the regulation of miR-29a expression could be an important issue to further elucidate the molecular action of curcumin in attenuating renal fibrosis. Based on the notion, crosstalk among multiple signaling pathways could be potentially required for the regulation of miR-29a expression. TGF-β is known as a key regulator of several microRNAs in diabetic nephropathy and renal fibrosis [22,39,40]. It has been reported that TGF-β1 signaling may participate in the regulation of miR-29a expression. In primary mesangial cells or podocytes, TGF-β1 signaling could suppress the expression of miR-29 family under high glucose conditions [41]. In the established unilateral ureteral obstruction nephropathy model, TGF-β/smad3 signaling has also been shown to negatively regulate miR-29 expression, which is critical for promoting renal fibrosis [42]. In future work, it will be interesting to know the detailed association between these complicated signaling networks, and whether curcumin treatment could modulate these signal transduction processes in some way.

Despite promising results for the use of curcumin in treating diabetic fibrosis in our studies, there are at least two issues that need to be addressed in future. First, due to the poor bioavailability of curcumin in humans, its clinical application has been greatly limited [43]. Currently, several strategies that counteract curcumin poor absorption and rapid metabolism and elimination from the body have been increasingly attempted, such as curcumin in hydrophilic nanoparticles, in the lipid-based formulation, or in a micellar system [43]. The improvement of the pharmacokinetic profile and the cellular uptake of curcumin is still challenging. On the other hand, although oral administration is the most common route for the delivery of curcumin, some studies have shown that as compared to oral administration, mice administered curcumin by intraperitoneal injection displayed higher concentrations of curcumin reached in target tissues such as brain [43,44,45]. Thus, intraperitoneal injection of curcumin in animals was chosen in the present study.In the future, improving bioavailability of curcuminand selectinga proper administration routewould be important for its application in treating diabetic kidney disease. Second, growing evidence has shown that the sleep circadian rhythm significantly associates withthe expression of mircoRNA including mir-29a [46]. Due to the fact that miR-29a is rhythmically expressed and involves the regulation of core clock components, mice that were intraperitoneally injected with curcumin or were sacrificed at different Zeitgeber times (ZT) or circadian times (CT) may probably lead to differential outcomes. In our study, we routinely perform animal experiments (including the intraperitoneal injection of curcumin or animal sacrifice) at a specific time period (from 10:00 a.m. to 3:00 p.m.). Therefore, to avoid animal research confounded by temporal expression of miR-29a, it may be necessary to include circadian interventions into our experimental design in the future.

5. Conclusions

In summary, our study presents a new mechanism of action for curcumin as an antifibrotic agent. We demonstrate that curcumin can rescue the dysregulated miR-29a/CB1R signaling pathway in renal glomeruli of diabetic mice to ameliorate renal fibrosis. These findings may be helpful in providing further insights into the complicated actions of curcumin as a renoprotective drug.