Background
Diabetic nephropathy (DN) is a major microvascular complication of diabetes and the leading cause of end-stage renal disease (ESRD) in many developed countries [
1]. DN is characterized by the increase in the glomerular filtration rate with intraglomerular hypertension and clinically progressive albuminuria followed by eventual loss of renal function [
2,
3]. Podocyte is an important component of the glomerular filtration barrier and plays a critical role in renal function injuries in DN [
4]. Podocyte damage is mainly manifested as the retraction of their foot processes, detachment, and abnormal expression of key proteins such as nephrin and podocin, which lead to a series of renal structure abnormalities including glomerular basement thickening, mesangial expansion and glomerulosclerosis [
5‐
9]. The general clinical use of multitudinous interventions focused on managing hyperglycemia and high blood pressure do not efficiently lower or reverse the progression of nephropathy, and a considerable proportion of diabetic patients still suffer from progressive and severe renal injury [
10‐
12]. Therefore, there is an urgent need to develop new and effective renoprotective approaches to the treatment of DN.
In China, traditional Chinese medicine (TCM) has been in practice for thousands of years in the treatment of diabetes and its complications [
13], showing a number of remarkable results and becoming more popular worldwide [
14,
15]. Wenshen Jianpi recipe (WSJPR) is a TCM preparation developed from famous and experienced TCM doctors, which consists of seven herbs (
Aconiti Lateralis Radix Praeparata,
Zingiber officinale Roscoe,
Radix Codonopsis, Rhizoma
Atractylodis macrocephalae,
Poria cocos, Radix
Paeoniae Alba,
Glycyrrhiza uralensis)
. In our earlier investigation, the therapeutic effects of four kinds of TCM on streptozotocin (STZ) induced DN rats were observed and WSJPR has shown significant effect on decreasing proteinuria. However, the therapeutic mechanisms of this herbal combination are not clear.
In the current investigation, the STZ induced DN rat model was used to evaluate the effects of WSJPR on renal function and renal pathological changes and the potential causal mechanisms.
Methods
Drugs
WSJPR is composed of seven raw materials listed in Table
1 [
16] and the dried herbs were provided by Ningbo Municipal Hospital of Traditional Chinese Medicine, Zhejiang, China. The herbal materials were morphologically identified by Dr. Wenbo Gong. Voucher specimen of each species was deposited at Ningbo Municipal Hospital of Traditional Chinese Medicine. The crude drugs were boiled with distilled water for 5 h and filtered. The filtered liquid was condensed to a concentration of approximately 3 g/ml, stored at 4 °C and diluted with distilled water before use [
16].
Table 1
The composition of WSJPR
Aconitum lycoctonum
| 6-11 g |
Zingiber officinale
| 6 g |
Codonopsis pilosula
| 15 g |
Atractylodes macrocephala
| 15 g |
Wolfiporia extensa
| 15 g |
Paeonia lactiflora
| 15 g |
Glycyrrhiza uralensis
| 3 g |
Animals
Male, 6-week-old healthy Sprague Dawley (SD) rats (240 g–280 g) were purchased from Shanghai Experimental Animal Centre, Chinese Academy of Sciences. All animals were housed in a specific-pathogen-free facility with ad libitum access to food and water under a constant temperature (23 ± 1 °C) and a 12-h light/dark cycle. This study was carried out in accordance with the recommendations of the Guidelines for the Care and Use of Laboratory Animals of the Ministry of Science and Technology of China. The protocol was approved by the Institutional Animal Care and Use Committee at Zhejiang Chinese Medical University Laboratory Animal Research Center (Zhejiang, China) (Approval Number: IACUC-20190225-05).
Experimental procedures
Streptozotocin (STZ, Sigma, USA) was used to induce diabetes as described previously [
17‐
19]. All the 58 rats were limited to water access for 12 h before the experiments. 50 rats were administered by a single intraperitoneal injection of 60 mg/kg body weight of STZ dissolved in citrate buffer (0.1 mol/L, pH 4.5). On day 15, the fasting blood glucose (FBG) levels of diabetic animals were measured and those with persistent hyperglycemia over 16.7 mmol/L were selected as diabetes. 40 randomly selected diabetic rats were then divided into five groups: STZ control; STZ + WSJPR 7.5 g/kg; STZ + WSJPR 15 g/kg; STZ + WSJPR 30 g/kg; STZ + valsartan 25 mg/kg (positive control group). The remaining eight rats received one dose intraperitoneal injection of citrate buffer only were used as normal control group. The rats were then administrated saline 10 mL/kg (normal and STZ controls), three different concentration of WSJPR or valsartan 25 mg/kg by an oral gavage method once a day for 8 weeks. Body weight, urinary volume, and biochemical parameters were monitored every 2 weeks. The rats were anaesthetized by intraperitoneal injection of 3% pentobarbital sodium (45 mg/kg) for the measurements of microcirculatory blood flow in the renal cortex. At the end of the experiments, rats were sacrificed by cervical dislocation and kidneys were excised and kept in liquid nitrogen before tests.
Biochemical analysis
Body weight of rats was measured at one week intervals. Blood was sampled at 2-week intervals for measurement of FBG, blood urea nitrogen (BUN), serum creatinine (Cr), total protein (TP) and albumin (ALB). The measurements of these indexes were conducted by using standard biochemical kits (Jiancheng, Institute of Biotechnology, China), respectively. 24-h urine of each rat was collected individually by metabolic cage at 2-week intervals. Susequently, the urine volume, urine-glucose (U-GLU), urine-UN (UUN), urine-TP (U-TP) and urine-ALB (U-ALB) were tested and the excretion rate was assessed as: concentration * urine volume/24 h.
Measurements of blood flow and Hemorheology index
The microcirculatory blood flow measurements were performed in the renal cortex in each animal by laser doppler flowmeter (Moor, UK) and it was expressed as ml·min
− 1·g
− 1 [
20]. The blood samples were obtained from heart and heparin anticoagulant tubes were used as the sampling tubes. The systematical changes of hemorheology of all rats were investigated by SA-5600 automatic hemorheology detector (Succeeder, China) [
21].
Renal histological analysis
Kidney sections were fixed in 4% buffered paraformaldehyde, embedded in paraffin, sectioned at 4 μm thickness and stained with hematoxylin and eosin (HE) and periodic acid schiff (PAS) to assess the alterations of glomerular. The sections were examined with light microscopy (Olympus, Japan) and micrographs were obtained randomly with magnification of 400 × .
Reverse transcriptase polymerase chain reaction (RT-PCR)
Total RNA was extracted from the kidney tissue of SD rats with Trizol Reagent (Invitrogen, USA), quantitated by measuring the OD260 and OD280 ratio, and then digested with gDNA Eraser (Takara, China) to remove genomic DNA. RNA was reverse-transcribed using oligo-dT random primers, with the superscript II reverse transcriptase (Invitrogen, USA), following the manufacturer’s instructions. Aliquots of cDNA were amplified by PCR using primers specific for rat nephrin, podocin and a constitutively expressed housekeeping gene, β-actin. Primers for PCR were designed by primer 5.0 according to the Genebank sequence and synthesized by Sangon Biotech Co., Ltd. (Shanghai, China). PCR reactions were performed in 7500 Real-Time PCR system (Applied Biosystems, USA) using the following conditions: 95 °C for 30 s followed by 40 cycles of 95 °C for 5 s, 60 °C for 34 s, 72 °C for 40 s, and a final extension step at 72 °C for 10 min. The quantity of specific mRNA was normalized to the expression level of internal control β-actin mRNA.
Statistical analysis
Data were expressed as mean ± SD. Statistical comparisons were performed with one-way analysis of variance by GraphPad Prism 5.0. Differences with P value < 0.05 were considered statistically significant.
Discussion
The treatment of diabetes and its complications usually focus on insulin, angiotensin-converting enzyme inhibitor and angiotensin receptor blocker due to their approved efficacy in clinical and animal researches [
22,
23]. But these methods are also connected with side effects such as hypovolemia and high proportion of DN patients still progress to ESRD and require everlasting and costly dialysis [
24,
25]. Traditional herbal compounds offer a significant advantage and utility for the management of DN via diverse ways and are recognized as effective alternatives to conventional medicine [
26,
27]. The present research investigated the effect of a Chinese herbal formulation on structure and function in the kidney of DN rats and valsartan was used as positive control.
In the current study, we used the diabetic rats induced by STZ injection to examine the efficacy and therapeutic mechanisms of WSJPR in DN. The results indicated that FBG, BUN, and the excretion rate of U-GLU, U-TP, U-ALB, UUN were significantly increased and body weight, serum TP, ALB, Cr were significantly decreased in STZ-induced DN rats, and mesangial matrix expansion was observed in the glomeruli by HE and PAS staining. These data demonstrated the successful induction of DN. In the WSJPR treatment group, WSJPR efficiently attenuated diabetic renal injury via improvement of the serum TP and ALB, reduction of the excretion rate of U-TP, U-ALB, UUN and alleviation of mesangial matrix expansion and glomerular basement thickening. The results indicated that WSJPR could effectively improve renal function and ameliorate protein metabolism disorder in DN rats.
Hemodynamic and hemorheological changes are closely related to the progression of nephropathy. In the early stage of DN, renal hemodynamics were abnormal with high filtration, high perfusion and high internal pressure, which are important causes of urinary protein leakage and glomerular sclerosis [
28]. Measurement of blood flow in renal cortex can reflect the state of renal peripheral blood circulation and blood perfusion. Normally, the interlobar artery, arcuate artery and interlobular artery are successively decreased in renal cortical blood flow. The closer to the cortex endings, the lower the blood flow [
29]. In our study, the microcirculatory blood flow of renal cortex was significantly increased in STZ control group, which suggested that DN rats showed hemodynamic abnormalities with high glomerular filtration and perfusion. Treatment with WSJPR could strongly reduce blood flow and ameliorate microcirculation.
Hemorheological changes such as hypercoagulability, hyperviscosity and slow blood flow could accelerate renal impairment [
21]. This study showed that hematocrit, erythrocyte aggregation index and erythrocyte count were significantly increased in DN rats. Hematocrit is closely associated with whole blood viscosity. The elevated level of erythrocytre aggregation can make erythrocyte easily aggregate in a string and cause elevation of blood viscosity [
30]. Treatment with WSJPR (30 g/kg) could markedly decrease erythrocyte aggregation index and the pharmacological mechanism might be connected with the reduction of blood viscosity.
Interestingly, the significant effect of WSJPR on hyperglycemia was not observed in diabetic rats. A study has shown that protecting podocytes from hyperglycemia with podocyte-specific deletion of glucose transporter member 4 can prevent the progression of glomerular disease and diabetes-associated albuminuria independently of glucose uptake [
31]. The underlying mechanism of the effect of WSJPR on DN observed in the present study is, however, still unclear and needs further study. These results suggested that WSJPR had potential for use in the protection against DN with prevention of albuminuria and amelioration of renal function independent of blood glucose lowering pathways.
Nephrin and podocin are podocyte-associated proteins and have been proven to be an integral membrane protein of the slit diaphragm. Nephrin, expressed on lateral aspect extending into the slit diaphragm, regulates the cytoskeletal architecture and affects the shape and viability of podocytes, while podocin colocalizes and interacts with cytosolic tail of nephrin in the lipid rafts of the podocyte foot process cell membrane [
32‐
35]. In the present study, results showed that the down regulated expressions of renal nephrin and podocin mRNA were observed in STZ control rat compared to normal control and their transcriptional levels were increased significantly after the 8-week period treatment with WSJPR, which is in accordance with the protein expression trends of nephrin and podocin in STZ control and WSJPR treatment groups in our previous immunohistochemistry assay. These results suggested that the increased mRNA and protein levels of nephrin and podocin in WSJPR treatment group might be a main contributor reducing podocyte injury in STZ-induced DN rat. Furthermore, glomerular hypertrophy and hyperglycemia were also detrimental to podocytes [
36]. WSJPR treatment can attenuate glomerular hypertrophy and improve hyperglycemia, resulting in multiple protective effects against podocyte injury.
The present study has limitations as follows. First, the present work focused only on the critical associated proteins of the podocyte and did not further evaluate the signaling pathways involved in repairing podocyte injuries such as the mammalian target of rapamycin (mTOR) signaling pathway, which has been proven to be related to pathological damages in podocyte [
37]. Second, the level and effect of autophagy in podocyte injuries was not studied in the present work. Autophagy is a bulk degradation process involved in cytosol recycling and the disassembly of superfluous or damaged organelles that plays a key role in the repair of injured podocytes and contributes to maintaining podocyte function [
38]. Insufficient autophagy was involved in the pathogenesis of podocyte loss and significant proteinuria in DN [
39]. More studies should investigate the effects of WSJPR on mTOR/autophagy to explore the further therapeutic mechanism for DN.
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