Metoclopramide Causes Airway Smooth Muscle Relaxation Through Inhibition of Muscarinic M3 Receptor in the Rat Trachea
Autor: | Noboru Harada, Koji Sumikawa, Masakazu Yamaguchi, Osamu Shibata, Masataka Saito, Masami Niwa, Maki Yoshimura, Tetsuji Makita |
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Rok vydání: | 2004 |
Předmět: |
Male
medicine.medical_specialty Contraction (grammar) Carbachol Metoclopramide medicine.drug_class Muscle Relaxation Inositol 1 4 5-Trisphosphate Muscarinic Antagonists In Vitro Techniques Muscarinic Agonists Phosphatidylinositols Radioligand Assay chemistry.chemical_compound Piperidines Internal medicine Muscarinic acetylcholine receptor medicine Animals Phosphatidylinositol Rats Wistar Receptor Receptor Muscarinic M3 business.industry Muscarinic acetylcholine receptor M3 Muscle Smooth Receptor antagonist Rats Trachea Anesthesiology and Pain Medicine Endocrinology chemistry Antiemetics business Muscle Contraction medicine.drug |
Zdroj: | Anesthesia & Analgesia. :1325-1329 |
ISSN: | 0003-2999 |
DOI: | 10.1213/01.ane.0000111104.33104.51 |
Popis: | UNLABELLED Although metoclopramide, often used as an antiemetic, is reported to have an anticholinesterase action, the effect on airway smooth muscle remains unclear. We investigated the effect of metoclopramide on the contraction, phosphatidylinositol response, and binding affinity of muscarinic M(3) receptors in rat trachea preparations. Male Wistar rats were anesthetized and their tracheas excised and chopped into 3-mm-wide rings, 1-mm-wide slices, or frozen 10- microm-thick sections. Contraction was induced with 0.55 microM carbachol (CCh) and, 30 min later, metoclopramide (10 microM to 1 mM) was added. The slices were incubated with (3)[H]myo-inositol, 0.55 microM CCh, and metoclopramide, and the formation of (3)[H] inositol monophosphate was measured. A radioligand binding study was conducted to examine the effects of metoclopramide using [(3)H] 4-diphenylacetoxy-N-methyl-piperidine methobromide (4-DAMP), a muscarinic M(3) receptor antagonist, in sections of the trachea. Metoclopramide concentration dependently attenuated CCh-induced contraction and inositol monophosphate accumulation, and also attenuated the binding affinity of 4-DAMP to muscarinic M(3) receptors. The 50% inhibitory concentration of metoclopramide against the binding affinity of 4-DAMP to muscarinic M(3) receptors of rat trachea was 24 micro M. These findings suggest that the attenuation by metoclopramide of CCh-induced contraction and phosphatidylinositol response may be mediated through the muscarinic M(3) receptors. IMPLICATIONS We investigated the effect of metoclopramide on the contraction, phosphatidylinositol response, and binding affinity of muscarinic M(3) receptors in rat trachea preparations. Our findings suggest that the attenuation by metoclopramide of carbachol-induced contraction and phosphatidylinositol response may be mediated through the muscarinic M(3) receptors. |
Databáze: | OpenAIRE |
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