Alteration of M3subtype muscarinic receptors in the diabetic rat urinary bladder

Yat-Ching Tong, Juei Tang Cheng

Research output: Contribution to journalArticle

36 Citations (Scopus)

Abstract

The M3 receptor (M3-mAChR) is the major muscarinic subtype in the animal bladder responsible for detrusor contraction. The alterations in its protein quantity and biosynthesis during diabetic cystopathy were investigated. 3-month-old male Wistar rats were divided into two groups: (1) 2-week diabetic rats and (2) normoglycemic control rats. Diabetes was induced by a single intravenous injection of 60 mg/kg streptozotocin. The amount of M3 receptor protein in the rat bladder body tissue was measured by Western immunoblotting using monoclonal antibodies. For determination of M3 muscarinic receptor mRNA in the bladder tissue, the method of Northern blotting was employed. The results of the Western immunoblotting showed that the amount of M3-mAChR protein in the diabetic bladder was significantly increased by about 70.2 ± 8.5% when compared to the control bladder (p < 0.05, n = 8). Northern blotting demonstrated a 54.7 ± 6.0% increase of M3-mAChR mRNA in the diabetic bladder (p < 0.05, n = 8). The findings of the present study demonstrated an upregulation of M3-mAChR biosynthesis in the diabetic urinary bladder. This phenomenon offers an explanation of the increased contractility after muscarinic stimulation of the detrusor muscle of diabetic animals.

Original languageEnglish
Pages (from-to)148-151
Number of pages4
JournalPharmacology
Volume64
Issue number3
DOIs
Publication statusPublished - 2002 Feb 20

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Muscarinic Receptors
Urinary Bladder
Northern Blotting
Cholinergic Agents
Western Blotting
Muscarinic M3 Receptors
Messenger RNA
Protein Biosynthesis
Streptozocin
Intravenous Injections
Wistar Rats
Proteins
Up-Regulation
Monoclonal Antibodies
Muscles

All Science Journal Classification (ASJC) codes

  • Pharmacology

Cite this

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abstract = "The M3 receptor (M3-mAChR) is the major muscarinic subtype in the animal bladder responsible for detrusor contraction. The alterations in its protein quantity and biosynthesis during diabetic cystopathy were investigated. 3-month-old male Wistar rats were divided into two groups: (1) 2-week diabetic rats and (2) normoglycemic control rats. Diabetes was induced by a single intravenous injection of 60 mg/kg streptozotocin. The amount of M3 receptor protein in the rat bladder body tissue was measured by Western immunoblotting using monoclonal antibodies. For determination of M3 muscarinic receptor mRNA in the bladder tissue, the method of Northern blotting was employed. The results of the Western immunoblotting showed that the amount of M3-mAChR protein in the diabetic bladder was significantly increased by about 70.2 ± 8.5{\%} when compared to the control bladder (p < 0.05, n = 8). Northern blotting demonstrated a 54.7 ± 6.0{\%} increase of M3-mAChR mRNA in the diabetic bladder (p < 0.05, n = 8). The findings of the present study demonstrated an upregulation of M3-mAChR biosynthesis in the diabetic urinary bladder. This phenomenon offers an explanation of the increased contractility after muscarinic stimulation of the detrusor muscle of diabetic animals.",
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Alteration of M3subtype muscarinic receptors in the diabetic rat urinary bladder. / Tong, Yat-Ching; Cheng, Juei Tang.

In: Pharmacology, Vol. 64, No. 3, 20.02.2002, p. 148-151.

Research output: Contribution to journalArticle

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