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Astragalus Polysaccharides Ameliorate Diabetic Bladder Dysfunction via Normalization of Neuromuscular Conduction
Shaochan Liang1, Siyuan Xu1,2,3, ShengLian Ye1
1School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Astragalus polysaccharides (APS) effectively treat diabetic underactive bladder (UAB) by normalizing neuromuscular conduction. This study shows APS improves bladder function and neurotransmission in diabetic mice.
Area of Science:
- Pharmacology
- Urology
- Diabetology
Background:
- Underactive bladder (UAB) is a complication of diabetes mellitus (DM).
- Current pharmacological treatments for diabetic UAB are limited.
- Astragalus polysaccharides (APS) from *Astragalus membranaceus* show promise for diabetes and its complications.
Purpose of the Study:
- To investigate the effects and mechanism of APS on high-fat-diet-induced (HFD) diabetic UAB in mice.
- To evaluate APS's impact on neuromuscular conduction and neurotransmission in diabetic UAB.
Main Methods:
- Induction of diabetic UAB in mice using a high-fat diet (HFD).
- Administration of APS to HFD-induced diabetic mice.
- Assessment of glycemic control (fasting plasma glucose, insulin, HOMA-IR).
- Evaluation of bladder function parameters (capacity, residual volume, compliance, pressures, voiding efficiency).
- Analysis of detrusor muscle neuromuscular contraction and neurotransmitter levels (nNOS, VIP, ChAT, SP).
Main Results:
- APS significantly reduced hyperglycemia and improved insulin resistance in HFD mice.
- APS treatment normalized bladder capacity, compliance, pressures, and voiding efficiency.
- APS ameliorated hyporesponsiveness in purinergic and cholinergic-mediated detrusor contractions.
- APS modulated neurotransmission by downregulating nNOS and VIP, and upregulating ChAT and SP.
Conclusions:
- Astragalus polysaccharides ameliorate diabetic-induced underactive bladder.
- APS normalizes neuromuscular conduction, improving detrusor muscle function and neurotransmission.
- APS represents a potential therapeutic agent for managing diabetic UAB.
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