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논문 기본 정보

자료유형
학술저널
저자정보
Shin, Chang-Yell (Department of Pharmacology, College of Pharmacy, Chung Ang University) Lee, Yul-Pyo (Department of Pharmacology, College of Pharmacy, Chung Ang University) Song, Hyun-Ju (Department of Pharmacology, College of Pharmacy, Chung Ang University) Je, Hyun-Dong (Catholic University of Daegu) Sohn, Uy-Dong (Department of Pharmacology, College of Pharmacy, Chung Ang University)
저널정보
대한약학회 Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea 제30권 제6호
발행연도
2007.1
수록면
715 - 722 (8page)

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We investigated whether the signal mechanism for relaxation may be affected by inflammation of the cat esophagus. Acute esophagitis was induced by perfusion with 0.1N HCI at a rate of 1mL/min for 45 min over three consecutive days. We then isolated esophageal smooth muscle cells by enzymatic digestion with collagenase. We pre-contracted the isolated smooth cells with acetylcholine (ACh) (10$^{-5}$ M) and compared the agonist-induced relaxation of pre-contracted normal cells with those of esophagitic cells. Vasoactive intestinal polypeptide (VIP)caused a dose-dependent relaxation in normal cells, and this curve was down shifted in esophagitic cells. Sodium nitroprusside (SNP) or SIN-1 (NO donor) produced dose-dependent relaxation in normal cells, which was not affected by esophagitis. 8-Br-cGMP (a cGMP analog) also induced dose-dependent relaxation to a similar extort in both normal and esophagitic cells. Forskolin (a cAMP activator) or db-cAMP (a CAMP analog) produced dose-dependent relaxation in normal cells, and this relaxation curve was down shifted in esophagitic cells. Western blotting was used to determine what subtype of adenylyl cyclase was involved in the CAMP pathway. Western blot analysis of homogenates derived from esophageal smooth muscle using antibodies against adenylyl cyclase types II, III, IV and V/VI revealed the presence of type V and/or type VI only. This result suggests that relaxation via a cAMP-dependent pathway rather than a cGMP dependent-pathway is down regulated in cat acute esophagitis. This subsensitivity of the cAMP related pathway may be related to the activity of adenylyl cyclase V/VI.

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