Astragaloside IV Inhibits Mitochondrial-Dependent Apoptosis of the Dorsal Root Ganglion in Diabetic Peripheral Neuropathy Rats Through Modulation of the SIRT1/p53 Signaling Pathway

Abstract

Purpose

To investigate the effect of astragaloside IV (AS-IV) on mitochondrial-dependent apoptosis in the dorsal root ganglion of diabetic peripheral neuropathy (DPN) rats through the SIRT1/p53 pathway.

Methods

Diabetic rat model was induced by high-carbohydrate/high-fat diet and intraperitoneal injection of STZ. Diabetic rats were divided into three groups (n =16 per group): DPN group, AS-IV group (60mg/kg/d) and α-lipoic acid (ALA) group (60mg/kg/d). Weight and blood glucose levels were monitored every 4 weeks for 12 weeks. DPN was evaluated using the Von Frey Filaments Test and nerve conduction velocity. The dorsal root ganglia of rats were isolated and the pathological changes of mitochondria were observed by electron microscopy. The activity of mitochondrial electron transport chain complex, mitochondrial membrane potential, malonaldehyde (MDA) and glutathione (GSH) levels were measured. Neural apoptosis was detected using the Terminal Deoxynucleotidyl Nick-End Labeling (TUNEL) assay kit. The cleaved caspase-3, major proteins in the SIRT1/p53 pathway, including SIRT1, acetyl p53, Drp1, BAX, and BCL-2, were detected using immunohistochemistry and Western blot. Gene expression of major proteins in the SIRT1/p53 pathway was also detected.

Results

After 12 weeks of treatment, AS-IV and ALA did not significantly affect body weight or fasting glucose levels, but reduced mechanical abnormal pain in DPN and improved nerve conduction velocity. AS-IV and ALA increased the level of GSH and decreased the level of MDA. Both AS-IV and ALA can reduce mitochondrial damage, improve mitochondrial electron transport chain complex activity and mitochondrial membrane potential, and reduce the percentages of positive cells with DNA fragmentation and the expression of cleaved caspase-3 protein. AS-IV and ALA up-regulated the expression of SIRT1 and down-regulated the expression of acetyl-p53, Drp1 and the ratio of BAX to BCL-2. Changes in gene expression were similar.

Conclusion

AS-IV can reduce the occurrence of mitochondrial-dependent apoptosis by regulating the SIRT1/p53 pathway. It has a similar therapeutic effect as ALA and is therefore a promising drug for the potential treatment of DPN.

Introduction

Diabetic peripheral neuropathy (DPN) is one of the most common chronic complications in diabetic patients, and its prevalence can reach 50%.¹ This condition is characterized by pain, paresthesia, and sensory loss. In severe cases, refractory ulcers may appear, which may eventually lead to amputation of the affected limb. Unfortunately, successful treatment and prevention remain challenging due to a lack of knowledge regarding the mechanisms of DPN development.² Studies have shown that strict glycemic control ameliorates but does not reverse neuropathy in type 1 patients.^3,4 By contrast, glycemic control is relatively ineffective in preventing diabetic neuropathy in type 2 diabetes.⁵

Mitochondrial damage in dorsal root ganglion (DRG) neurons, axons and Schwann cells has been proposed as a unifying mechanism for diabetic neuropathy.^6–10 Studies have shown that p53 promotes apoptosis by regulating mitochondrial fission.¹¹ p53 can be transported from the nucleus to the cytoplasm, where it assists in translocating Drp1 to the mitochondrial surface,¹² causing the mitochondria to split into several fragments and affecting its function.¹³ At the same time, p53 can upregulate BAX expression downregulate BCL-2 expression, increase the permeability of the mitochondrial outer membrane, and induce cytochrome C release from the mitochondrial intermembrane space to initiate apoptosis.

Sirtuin 1 (SIRT1) is a protein deacetylase that depends on nicotinamide adenine dinucleotide (NAD+). SIRT1 catalyzes the deacetylation of p53 at K382.^14,15 Based on recent studies, the generally held view is that the function of p53 is inhibited by deacetylation of K382 at the C-terminus.^16,17 The inhibition of p53 function may be a major mechanism for the anti-aging and cell survival-promoting function of SIRT1.^8,18–20

Astragaloside IV (AS-IV) is a biologically active saponin isolated from Astragalus root. Some studies on neurodegenerative diseases (such as Parkinson’s disease and Alzheimer’s disease) have shown that AS-IV has a protective effect on mitochondrial damage and can inhibit neuronal apoptosis.^21–23 In addition, AS-IV also has a strong anti-oxidative stress effect.^24,25 α-Lipoic acid (ALA) is a well-known antioxidant and has been widely used to treat DPN.^26,27 Studies have found that it can up-regulate SIRT1 expression.^28,29 Based on the above beneficial effects, we speculate that AS-IV can protect mitochondria and inhibit the apoptosis of dorsal root ganglion neurons through the SIRT1/p53 pathway. Therefore, in this experiment, we used ALA as a positive control to study the beneficial effects of AS-IV on the dorsal root ganglia of diabetic rats induced by streptozotocin adjuvant and a high-carbohydrate/high-fat diet. Our research aimed to provide some clues to prove that AS-IV may be an effective and feasible drug candidate for the treatment of diabetic peripheral neuropathy.

Materials and Methods

Animals

Sixty-four male Sprague Dawley rats (3 weeks old, 110±10 g) were purchased from Vital Rive Experimental Animal Technology Co., Ltd. (Beijing, China) SCXK [Beijing] 2016-0006. The animals were placed in a 12 h/12 h artificial light–dark cycle environment with a temperature of 22–24 °C and a humidity of 40%. The animals were kept in 16 cages with 4 rats in each cage, and the bedding was changed daily. All of the following experiments complied with the “Guiding Principles for the Care and Use of Laboratory Animals” promulgated by the National Science and Technology Commission of China.

Induction of Diabetes and Drug Treatment

Sixteen rats were randomly selected as the control group and given a standard diet. The remaining 48 rats were fed a high-carbohydrate/high-fat diet (67% standard diet, 10% lard, 20% sucrose, 2.5% cholesterol, and 0.5% sodium cholate) for 6 weeks and were then intraperitoneally injected with streptozotocin (STZ) (Sigma-Aldrich, St Louis, MO, USA) (25 mg/kg) twice with an interval of 2 days. One week after the injection of STZ, animals with fasting blood glucose levels of ≥16.7 mmol/L were used as diabetic animals and continued to be fed a high-carbohydrate/high-fat diet. Forty-eight diabetic rats were randomly divided into the DPN group, DPN plus ALA group, and DPN plus AS-IV group, with 16 rats in each group. The DPN plus ALA group was given 60 mg/kg of ALA (Sigma-Aldrich, St Louis, MO, USA) by intragastric administration daily, while the DPN plus AS-IV group was given 60 mg/kg of AS-IV (Chengdu Herbpurify Co., Ltd. Chengdu, China) daily; the control group and DPN group received the same amount of normal saline by intragastric administration every day. The drug treatment lasted 12 weeks.

Fasting Blood Glucose and Weight

The successful induction of diabetes was recorded as week 0. The fasting blood glucose and body weight of the rats in each group were measured at the 4th, 8th and 12th week, respectively.

Mechanical Hyperalgesia

As described in Ueda and Neyama,³⁰ the electronic von Frey anesthesia instrument was used to detect the pain threshold of the experimental rats (type 2390, 90 g probe, 0.8 mm diameter; IITC Life Science Inc., Woodland Hills, CA, USA). The rigid tip was used to mechanically stimulated the middle of the plantar surface of the rat hind paw, and the pressure required to induce the withdrawal response was defined as the pain threshold, which was recorded in grams. The test was repeated once every 5 minutes, with five measurements for each animal, and the average value was calculated.

Nerve Conduction Velocity (NCV)

After the experimental rats were anesthetized with 3% by volume isoflurane, 1e1.2% isoflurane was added to oxygen through a mask to maintain anesthesia, and the rats were fixed in the prone position. Stimulating and recording platinum wire electrodes were placed directly under the sciatic nerve trunk of right leg. A piece of skin between the biceps femoris and semitendinous muscles was incised and detached to expose sciatic nerve at two sites to attach electrodes. Stimulation electrode was placed at the sciatic nerve notch. Sciatic nerve was stimulated with single square waves pluses (1.2 V in intensity, 1 ms in width) through the Functional Experiment System (BL-420s, Taimeng, Sichuan, China). Action potential latency (L) of sciatic nerve and the distance (D) between the two electrodes were measured to calculate the motor NCV (MNCV), MNCV = D/L(m/s). Sensory NCV (SNCV) was measured and recorded by exchanging the electrode of stimulation and that of recording. Stimulation parameters and SNCV calculation procedure were the same as MNCV methods.

Histopathology and Immunohistochemistry

Electron microscopy: The L4-5 dorsal root ganglia were fixed in 4% glutaraldehyde and treated with 1% OsO4 in 0.1 M PBS. The samples were dehydrated through successive application of graded acetone solutions and embedded in EPON 812. Ultrathin sections (70 nm) were placed on a copper grid and stained with uranyl acetate and lead citrate. The samples were observed by transmission electron microscopy (TEM, JEM-1230, Tokyo, Japan). Pathological changes of mitochondria in neurons were assessed. The level of intact mitochondria was determined using the published Mitochondrial Quality Index (MQI).³¹ Briefly, individual mitochondria were assigned one of the following grades: 1 – fully intact, 2 – disruption of the cristae (typically from swelling or loss of integrity of the inner membrane), 3 – disruption of the outer mitochondrial membrane, and 4 – disruption of the cristae and the outer membrane.

Immunohistochemistry: The L4-5 dorsal root ganglia were quickly collected and fixed in 4% paraformaldehyde overnight. The tissue was then paraffinized and cut into 4 μm sections. The sections were deparaffinized, the antigen was repaired with citric acid solution (0.01 mol/L, pH 6.0), and the sections were then incubated with 3% H₂O₂ to reduce nonspecific background staining caused by endogenous peroxidase. The sections were blocked with non-immunoreactive serum and then incubated with antibodies against SIRT1, acetyl-p53, Drp1, BAX, BCL-2, and cleaved-caspase-3 at 4 °C overnight. The next day, the sections were incubated with goat anti-rabbit (Beijing noble Ryder Technology Co., Ltd., Beijing, China), stained with diaminobenzidine (DAB) chromogen, and then counterstained with hematoxylin. We observed and analyzed the sections using an optical microscope (Olympus, Bx53F, Tokyo, Japan). The primary antibodies were used in the following dilutions: SIRT1, 1:200 (Abcam, Cambridge, UK); acetyl-p53, 1:200 (Abcam, Cambridge, UK); Drp1, 1:400 (Abcam, Cambridge, UK); BAX, 1:400 (Protaintech, Rosemont, IL, USA); BCL-2, 1:200 (Affinity Bioscience, Cincinnati, OH, USA); and cleaved caspase-3, 1:200 (Cell Signaling, Danvers, MA, USA).

Mitochondrial Function

The mitochondria were extracted from the dorsal root ganglion according to the method of the Animal Tissue Active Mitochondria Isolation Kit (Genmed Scientifics Inc., Ellington, TX, USA).

The activity of complex I, II, III and IV in the mitochondrial electron transport chain was detected by chemical colorimetry (Genmed Scientifics Inc., Ellington, TX, USA). Complex I activity was measured by the oxidation of NADH by ubiquinone-1 at 340 nm, complex II activity was measured by the oxidation of succinate by ubiquinone-2 at 600 nm, complex III activity was assayed by the reduction of cytochrome C by ubiquinol-2 at 550 nm, and complex IV activity was assayed by the oxidation of dithionite-reduced cytochrome C at 550 nm. Assays for complexes I and III were done in the presence and absence of the specific inhibitors rotenone and antimycin A, respectively, to evaluate the contribution of contaminant activities. The final concentration of total proteins was determined by the method of Lowry et al.³² The activity of the complex was expressed as the rate at which each complex in the unit protein reduced the substrate in the catalytic reaction (U/mg/min).

The measurement of mitochondrial membrane potential was performed according to the protocol of the Mitochondrial Membrane Potential Detection Kit (Genmed Scientifics Inc., Ellington, TX, USA). The mitochondrial samples were incubated with 5,5ʹ,6,6ʹ-tetrachloro-1,1ʹ,3ʹ-tetraethylbenzimidazolcarbocyanine iodide staining working solution at room temperature for 10 minutes. Relative fluorescence units (RFUs) were obtained by measuring the excitation/emission wavelengths at 490/590 nm with a fluorescence microplate reader (BioTek, Synergy H4, Winooski, VT, USA). The mitochondrial membrane potential was expressed as RFU per mg of protein (RFU/mg).

Oxidative Stress Markers

As markers of oxidative stress, glutathione (GSH), and malondialdehyde (MDA) levels of the dorsal root ganglion were measured by a microplate reader (BioTek, Synergy H4, Winooski, VT, USA) using the assay kits (Nanjing Jiancheng Bioengineering Research Institute, Nanjing, China) according to the procedure recommended by the manufacturer.

Apoptosis

Neuronal apoptosis was determined using a terminal deoxynucleotidyl nick-end labeling (TUNEL) assay kit according to the manufacturer’s protocol (Roche, Basel, Switzerland). The percentage of TUNEL-positive cells was calculated by dividing the number of nuclei that stained positive by the total number of nuclei in a given field of view (under 400× microscope magnification).

Western Blot Analysis

The protein of the isolated L4-5 dorsal root ganglia was extracted and separated by 8–12% sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and further transferred to polyvinylidene fluoride (PVDF) membranes. After blocking with 5% nonfat milk for 2 h, the PVDF membranes were incubated with specific primary antibodies at 4°Cover-night and washed. Membranes were incubated with secondary antibodies for 1 h. Detection was visualized using the Odyssey Infrared Imaging System (LI-COR, Inc., Lincoln, NA, USA) and analyzed with Image J software. The basal levels of proteins were normalized to levels of β-actin protein. The primary antibodies were used in the following dilutions: SIRT1, 1:400 (Abcam, Cambridge, UK); acetyl-p53, 1:500 (Abcam, Cambridge, UK); Drp1, 1:1000 (Abcam, Cambridge, UK); BAX, 1:2000 (Protaintech, Rosemont, IL, USA); BCL-2, 1:500 (Affinity Bioscience, Cincinnati, OH, USA); and cleaved caspase-3, 1:1000 (Cell Signaling, Danvers, MA, USA); β-actin,1:5000 (Abways, Shanghai, China).

Reverse Transcription-Quantitative Polymerase Chain Reaction Analysis (qPCR)

Total RNA was extracted from dorsal root ganglion using TRIzol (Invitrogen, Thermo Fisher Scientific, Inc., Waltham, MA, USA) according to the manufacturer’s protocol. cDNA was synthesized from mRNA using a RevertAid First Strand cDNA Synthesis Kit (Thermo Fisher Scientific, Inc. Waltham, MA, USA), followed by qPCR using a SYBR^® Green PCR Master Mix (Applied Biosystems; Thermo Fisher Scientific, Inc. Waltham, MA, USA) and the StepOnePlus sequence detection system (Applied Biosystems; Thermo Fisher Scientific, Inc. Waltham, MA, USA). Cycling conditions of the reactions were as follows: 10 min of predenaturation at 95 °C followed by 40 cycles of 15 s denaturation at 95 °C and 60 s of annealing at 60 °C. The sequences of the primers used are listed in Table 1. The housekeeping gene β-actin was used for normalization.

Table 1.

Primer Information for the RT-PCR

Gene	Database Accession Number	Forward Primer (5ʹ–3ʹ)	Reverse Primer (5ʹ–3ʹ)
SIRT1	NM_001372090.1	AGATTTCAAGGCTGTTGGTTCC	CAGCATCATCTTCCAAGCCATT
p53	XM_006246594.3	CAGCGACAGGGTCACCTAATTC	GGCAGAACAGCTTATTGAGGGA
Drp1	NM_053655.3	TCCAGCTCATTACCAAGTTTGC	CAGATTCTAAGGTTCGCCCAAA
BAX	NM_017059.2	GGCGATGAACTGGACAACAAC	CCCAGTTGAAGTTGCCGTCT
BCL-2	NM_016993.1	TTGTGGCCTTCTTTGAGTTCG	GCATCCCAGCCTCCGTTAT
β-Actin	NM_031144	TGCTATGTTGCCCTAGACTTCG	GTTGGCATAGAGGTCTTTACGG

Statistical Analysis

The statistical analysis software SPSS 24.0 was used to analyze the data, and the measurement data were described by the mean ± standard deviation (SD). First, analysis of variance was performed for the comparison of multiple groups, and then the Tukey’s test was used for multiple comparisons. Statistical tests were performed using two-sided tests, and P ≤ 0.05 was considered to indicate statistically significant differences.

Results

The Fasting Blood Glucose and Weight

As shown in Figure 1A, STZ-injected rats displayed hyperglycemia. Diabetic rats had significantly higher fasting blood glucose levels compared to rats in the control group (p < 0.001). ALA or AS-IV treatment did not bring about any significant changes in the fasting blood glucose levels of DPN rats. As shown in Figure 1B, the weights of diabetic rats at the 4th, 8th and 12th week were not significantly different from that of the control group.

Figure 1.

Effects of AS-IV on fasting blood glucose and body weight in diabetic rats at 12 weeks.

Notes: Fasting blood glucose levels (A) and body weight (B) were measured every 4 weeks. Data are represented as mean ± SD. ***P < 0.001 vs control group.

Abbreviations: SD, standard deviation; DPN, diabetic peripheral neuropathy; AS-IV, astragaloside IV; ALA, α-lipoic acid.

Pain Thresholds

STZ-injected rats displayed mechanical hyperalgesia. Diabetic rats were less tolerant to pressure applied to the paw as compared to rats in the control group. ALA or AS-IV treatment was able to significantly reduce mechanical hyperalgesia of the hind paws of DPN rats (p < 0.01), as shown in Figure 2.

Figure 2.

Effects of AS-IV on paw withdrawal thresholds.

Notes: Data are represented as mean ± SD. *P < 0.05, **P < 0.01, ***P < 0.001 vs control group. ^##P < 0.01 vs DPN group.

Abbreviations: SD, standard deviation; DPN, diabetic peripheral neuropathy; AS-IV, astragaloside IV; ALA, α-lipoic acid.

Nerve Conduction Velocity

The DPN group rats had significant decreases in the MNCV and SNCV compared with the control group rats. The MNCV and SNCV of the two groups of rats treated with ALA and AS-IV were higher than those in the DPN group (Figure 3A and B).

Figure 3.

Effect of AS-IV on NCV.

Notes: (A) MNCV; (B) SNCV. Data are represented as mean ± SD. *P < 0.05, **P < 0.01; ***P < 0.001  vs control group. ^#P < 0.05, ^##P < 0.01 vs DPN group.

Abbreviations: NCV, nerve conduction velocity; MNCV, motor nerve conduction velocity; SNCV, sensory nerve conduction velocity; SD, standard deviation; DPN, diabetic peripheral neuropathy; AS-IV, astragaloside IV; ALA, α-lipoic acid.

The decrease of NCV and the mechanical hyperalgesia validated the DPN model.³³

Mitochondrial Morphology

In the control group, dorsal root ganglion neurons were rich in mitochondria and had normal structures. The inner and outer mitochondrial membranes and mitochondrial cristae were intact and well distributed. In the DPN group, the mitochondria of dorsal root ganglion neurons were swollen and degenerated, the outer mitochondrial membrane was damaged, and the mitochondrial cristae were broken, sparse, or had even disappeared, and most showed vacuolar changes. Mitochondria are the most destructive, with the highest MQI score (4 points). The mitochondria of DRG neurons in the DPN plus ALA and DPN plus AS-IV groups were slightly swollen, with a relatively complete structure and clear mitochondrial cristae. The MQI score of most mitochondria was 2–3. The mitochondrial damage in rats treated with ALA and AS-IV was alleviated compared with the DPN group (Figure 4A and B).

Figure 4.

Effect of AS-IV on mitochondrial pathomorphology.

Notes: (A) Electron micrographs illustrated the intact mitochondria (white arrows). Scale bar, 1 µm. (B) Mitochondria quality index score. Data are represented as mean ± SD. *P < 0.05, **P < 0.01, ***P < 0.001 vs control group. ^##P < 0.01, ^###P < 0.001 vs control group.

Abbreviations: SD, standard deviation; DPN, diabetic peripheral neuropathy; AS-IV, astragaloside IV; ALA, α-lipoic acid.

Mitochondrial Function

The measured activity of complex I, II, III, and IV in the mitochondrial electron transport chain is shown in Figure 5A–D. Complex I, II, III, and IV activities were significantly lower in the DPN than the control group (p < 0.01). The levels of the two groups of rats treated with ALA and AS-IV were restored and were higher than those in DPN animals (p < 0.05). The activities of complex I, II, III of the two groups of rats treated with ALA and AS-IV were not statistically different from that of the control group, and the activity of compound IV was lower than that of the control group (p < 0.05).

Figure 5.

Effect of AS-IV on mitochondrial electron transport chain complex activity.

Notes: (A) Mitochondrial electron transport chain complex I activity. (B) Mitochondrial electron transport chain complex II activity. (C) Mitochondrial electron transport chain complex III activity. (D) Mitochondrial electron transport chain complex IV activity. Data are represented as mean ± SD. *P < 0.05, **P < 0.01, ***P < 0.001 vs control group. ^#P < 0.05 vs DPN group.

Abbreviations: SD, standard deviation; DPN, diabetic peripheral neuropathy; AS-IV, astragaloside IV; ALA, α-lipoic acid.

As shown in Figure 6, the mitochondrial membrane potential of the dorsal root ganglion of DPN rats was significantly decreased compared with control rats (p < 0.001), and that of the ALA or AS-IV treatment group also decreased (p < 0.01). The mitochondrial membrane potential was higher in the two groups of animals treated with ALA and AS-IV than in DPN animals (p < 0.05).

Figure 6.

Effect of AS-IV on mitochondrial membrane potential.

Notes: Data are represented as mean ± SD. **P < 0.01, ***P < 0.001  vs control group. ^#P < 0.05 vs DPN group.

Abbreviations: SD, standard deviation; DPN, diabetic peripheral neuropathy; AS-IV, astragaloside IV; ALA, α-lipoic acid.

Oxidative Stress Markers

As shown in Figure 7A, the content of MDA in the dorsal root ganglia of diabetes rats was higher than that in the control group. The MDA content of the two groups of rats treated with ALA and AS-IV was lower than that of the DPN group (p < 0.01).

Figure 7.

Effect of AS-IV on oxidative stress.

Notes: (A) MDA, (B) GSH. Data are represented as mean ± SD.*P < 0.05, **P < 0.01; ***P < 0.001 vs control group.  ^#P < 0.05, ^##P < 0.01 vs DPN group.

Abbreviations: MDA, malonaldehyde; GSH, glutathione; SD, standard deviation; DPN, diabetic peripheral neuropathy; AS-IV, astragaloside IV; ALA, α-lipoic acid.

As shown in Figure 7B, compared with the control group, the level of GSH in the dorsal root ganglia of the DPN group decreased (p < 0.05). The GSH levels of the two groups of rats treated with ALA and AS-IV were lower than those in the DPN group (p < 0.05).

Neuronal Apoptosis

As can be seen from Figure 8A and B, TUNEL staining micrographs showed an increased percentage of positive cells with DNA fragmentation in the DPN group (p < 0.001), with a comparatively lower percentage of positive cells with DNA fragmentation observed in the two groups of rats treated with ALA and AS-IV (p < 0.05). As shown in Figure 8C and D, the expression of cleaved caspase-3 in diabetic rats was significantly up-regulated compared with the control group (p < 0.001). Compared with the DPN group, the expression of cleaved caspase-3 was down-regulated in the two groups of rats treated with ALA and AS-IV (p < 0.001).

Figure 8.

Effect of AS-IV on apoptosis.

Notes: (A and B) The results of TUNEL staining. Scale bar, 50 µm. (C) Immunohistochemical staining of cleaved caspase-3. Scale bar, 50 µm. (D) The cleaved caspase-3 expression was measured by Western blot. Data are represented as mean ± SD. *P < 0.05, ***P < 0.001 vs control group.  ^###P < 0.001, ^#P < 0.05 vs DPN group.

Abbreviations: TUNEL, terminal deoxynucleotidyl nick-end labeling; SD, standard deviation; DPN, diabetic peripheral neuropathy; AS-IV, astragaloside IV; ALA, α-lipoic acid.

SIRT1/p53 Signaling Pathway

The expression of related proteins in the SIRT1/p53 signaling pathway was evaluated by IHC. The positive expression of SIRT1 was mainly observed in the nucleus and partly in the cytoplasm. Acetyl-p53, Drp1, BAX, and BCL-2 were observed in the cytoplasm (Figure 9).

Figure 9.

Immunohistochemical staining of SIRT1, acetyl-p53, Drp1, BAX, BCL-2. Scale bar: 50 µm.

Abbreviations: DPN, diabetic peripheral neuropathy; AS-IV, astragaloside IV; ALA, α-lipoic acid.

As shown in Figure 10A and B, Western blot analysis showed that the expression of SIRT1 in the two groups of rats treated with ALA and AS-IV was significantly up-regulated compared with the DPN group (p <0.05). As shown in Figure 10A and C, compared with the control group, the expression of acetyl-p53 in diabetic rats was significantly up-regulated (p <0.001). The expression of acetyl-p53 in the two groups treated with ALA and AS-IV was significantly lower than that in the DPN group. As shown in Figure 10A and D, the expression of Drp1 in DPN group and ALA group was higher than that in the control group. Compared with the DPN group, the expression of Drp1 was down-regulated in the two groups treated with ALA and AS-IV. Analysis of the ratio of BAX to BCL-2 showed that the ratio in the DPN group was higher than that in the control group (p <0.001). Compared with the DPN group, the ratio of BAX to BCL-2 in the two groups treated with ALA and AS-IV decreased (Figure 10A and E).

Figure 10.

Western blot analysis of SIRT1, acetyl-p53, Drp1, BAX, BCL-2.

Notes: (A) Films of SIRT1, acetyl-p53, Drp1, BAX, BCL-2, and β-actin bands. (B–D) Levels of SIRT1 (B), acetyl-p53 (C), Drp1 (D) expressed as the optical density value normalized to β-actin. (E) Ratio of optical density value of BAX to BCL-2. Data are represented as mean ± SD. *P < 0.05, ***P < 0.001  vs control group. ^#P < 0.05, ^##P < 0.01, ^###P < 0.001 vs DPN group.

Abbreviations: SD, standard deviation; DPN, diabetic peripheral neuropathy; AS IV, astragaloside IV; ALA, α-lipoic acid.

To explore the underlying mechanism of AS-IV inhibiting cell apoptosis, the expression of genes involved in the SIRT1/p53 pathway was assessed. The expression of SIRT1 in the two groups of rats treated with ALA and AS-IV was significantly up-regulated compared with the DPN group (p <0.01) (Figure 11A). Compared with the control group, the expression of p53 in the DPN group was up-regulated (p <0.001). The p53 expression of the two groups of rats treated with ALA and AS-IV was lower than that of the DPN group (p <0.001). (Figure 11B) Compared with the control group, the expression of Drp1 in the DPN group was significantly up-regulated (p <0.001). The expression of Drp1 in the two groups of rats treated with ALA and AS-IV was significantly lower than that in the DPN group (p <0.001) (Figure 11C). The expressions of BAX and BCL-2 in diabetic rats were higher than those in the control group. Compared with the DPN group, the expression of BAX in the two groups of rats treated with ALA and AS-IV was significantly down-regulated, while the expression of BCL-2 was up-regulated (p <0.001) (Figure 11D and E).

Figure 11.

mRNA expression of SIRT1, acetyl-p53, Drp1, BAX, BCL-2.

Notes: (A) SIRT1 mRNA expression, (B) p53 mRNA expression, (C) Drp1 mRNA expression, (D) BAX mRNA expression, (E) BCL-2 mRNA expression. Data are represented as mean ± SD. *P < 0.05, **P < 0.01, ***P < 0.001  vs control group. ^##P < 0.01, ^###P < 0.001 vs DPN group.

Abbreviations: SD, standard deviation; DPN, diabetic peripheral neuropathy; AS IV, astragaloside IV; ALA, α-lipoic acid.

Discussion

The main purpose of the experiment was to explore the therapeutic effect of AS-IV on DPN rats and its molecular mechanism. The current study evaluated the effect of AS-IV on the development of DPN rats induced by STZ. We found that AS-IV has a neuroprotective effect similar to ALA. Both of them can significantly alleviates hyperalgesia, increase nerve conduction velocity, and play a therapeutic role by regulating the SIRT1/p53 pathway to reduce mitochondria-dependent apoptosis.

Neuropathic pain is the most common impediment associated with DPN. Thus, measurement of allodynia and hyperalgesia in response to mechanical stimuli is considered an important, reliable, and sensitive index for neuropathic pain during DPN.³⁴ An array of researchers used various methods to evaluate allodynia and hyperalgesia during the experimental DPN, such as von Frey filaments test (Paw withdrawal response to light touch of plantar surface), Hargreaves method (Paw withdrawal response latency to escalating heat applied to the plantar surface), Paw intradermal formalin-evoked responses, Randall–Selitto test, etc.^34–36 In the present investigation, the results of the von Frey filaments test showed that the mechanical pain threshold of the DPN group was reduced, confirming the neuropathic pain of DPN, and the treatment of AS-IV and ALA can increase the mechanical pain threshold of DPN rats and reduce allodynia and hyperalgesia.

Electrophysiological assessment of nerve function in diabetic patients provides a quantitative measure of nerve integrity and a means to monitor disease onset and progression.³⁷ In rodent models of diabetic neuropathy, NCV measurements are commonly used to define the extent of nerve dysfunction as well as providing an endpoint in studies of putative treatments.³³ Our research results showed that the NCV of the DPN group decreased, which proved that STZ and high-carbohydrate/high-fat diet-induced diabetic rats had obvious neurological dysfunction. Interestingly, AS-IV and ALA can improve MNCV and SNCV in DPN rats, and their effects are similar.

Some evidence suggests that mitochondria play an important role in sensory neurons in the pathophysiology of abnormal pain.^38–40 In nerve cells, the position of mitochondria is particularly important. Mitochondria provide energy for various activities of neurons and are almost the exclusive providers of energy. Mitochondria are considered to be a key regulator of neuron-related complications in diabetes.⁴¹ A decrease in mitochondrial membrane potential is the key event initiating mitochondrial-dependent apoptosis. We observed that the mitochondria of DRG neurons in DPN rats were swollen and vacuolated, and the mitochondrial cristae disappeared. At the same time, the activity of complex I–IV in the mitochondrial electron transport chain and the mitochondrial membrane potential decreased, the expression of cleaved caspase-3 up-regulated, and the number of apoptotic cells increased. These are consistent with the results of other researchers.^6,7,42 AS-IV and ALA treatment can significantly reduce the structural damage of mitochondria, enhance the activity of the mitochondrial electron transport chain complex, protect and maintain the mitochondrial membrane potential, and improve mitochondrial function, thereby reducing cell apoptosis.

p53 is induced in damaged neurons and has a neurotoxic function in animal models of neurodegenerative disease.⁴³ p53 can cause the excessive fission of mitochondria mediated by Drp1. Excessive fission severely damages the mitochondrial genome, resulting in damage of the mtDNA that encodes the 13 polypeptides involved in oxidative phosphorylation and mitochondrial structure,⁴⁴ opening of the mitochondrial permeability transition pore (mPTP), and increased reactive oxygen species (ROS) production.⁴⁵ p53 can also reduce the mitochondrial membrane potential through the pro-apoptotic protein BAX, increase mitochondrial membrane permeability, release mitochondrial-related pro-apoptotic factors, and initiate the caspase cascade reaction to induce apoptosis.^46,47 In this study, acetyl-p53 was significantly expressed in DPN rats, downstream Drp1 and BAX expression was upregulated, and anti-apoptotic protein BCL-2 expression was downregulated. This suggests that apoptosis induced by p53-mediated mitochondrial destruction is an important molecular mechanism leading to DPN.

SIRT1 acts as a negative regulator of p53 to inhibit cell apoptosis.⁴⁸ The data of Shi et al showed that high concentrations of glucose can induce hippocampal neuronal apoptosis by downregulating SIRT1 and increasing p53 acetylation.⁴⁹ Studies have shown that ALA can activate SIRT1 and protect cardiomyocytes.⁵⁰ In our study, SIRT1 expression was up-regulated in DPN rats treated with AS-IV and ALA, indicating that SIRT1 is a neuroprotective target for AS-IV and ALA. The down-regulation of acetyl-p53 and Drp1 and the ratio of BAX to BCL-2 further confirmed that AS-IV and ALA can increase mitochondrial bioenergy and mitochondrial membrane potential through the SITR1/p53 pathway, and partially reverse the neuronal apoptosis induced by hyperglycemia.

ALA has been examined quite extensively as a treatment for diabetic neuropathy. Moreover, ALA was effective in the treatment of distal sensory motor neuropathy, as well as in the modulation of peripheral neuropathy and pain reduction in diabetic patients.⁵¹ Experimental evidence suggested that ALA could restore the glutathione levels, prevent lipid peroxidation, increase the activity of antioxidant enzymes (such as catalase and superoxide dismutase in peripheral nerves), increase the blood flow, along with NCV.^52–54 AS-IV is a natural bioactive compound isolated from Astragalus membranaceus Bunge, regarded as the critical marker to evaluate the quality of Astragalus membranaceus in the Chinese Pharmacopeia. Studies have found that AS-IV can prevent mitochondrial dysfunction of central neuron by increasing superoxide dismutase (SOD) and GSH, reducing MDA, and inhibiting oxidative stress.^55–57 In our experiments, both ALA and AS-IV reduced the MDA content in the dorsal root ganglia of DPN rats and increased the GSH level, and there was no significant difference in their antioxidant effects. At the same time, they have similar functions of protecting mitochondria and inhibiting neuronal apoptosis.

Conclusion

Our results showed that AS-IV can protect mitochondrial function and structure through the SIRT1/p53 pathway, reduce cell apoptosis, and protect peripheral nerves in diabetic rats (Figure 12). It has a similar therapeutic effect as ALA and is therefore a promising drug for the potential treatment of DPN.

Figure 12.

As-IV inhibits mitochondrial-dependent apoptosis through modulation of the SIRT1/p53 signaling pathway.

Funding Statement

This research was funded by the National Natural Science Foundation of China [grant number 81803922].

Institutional Review Board Statement

The study was approved by the Ethics Committee of Hebei University of Chinese Medicine (protocol code DWLL2018042, Dec 28, 2018).

Data Sharing Statement

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Disclosure

The authors declare no conflicts of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.