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Endocrinology Vol. 141, No. 8 2854-2860
Copyright © 2000 by The Endocrine Society


ARTICLES

Cocaine-Amphetamine-Regulated Transcript (CART) Acts in the Central Nervous System to Inhibit Gastric Acid Secretion via Brain Corticotropin-Releasing Factor System1

Toshikatsu Okumura, Hiroto Yamada, Wataru Motomura and Yutaka Kohgo

Third Department of Internal Medicine, Asahikawa Medical College, Asahikawa 078-8510, Japan

Address all correspondence and requests for reprints to: Toshikatsu Okumura, M.D., Third Department of Internal Medicine, Asahikawa Medical College, Asahikawa 078-8510, Japan. E-mail: okumurat{at}asahikawa-med.ac.jp

Recent study has indicated that cocaine-amphetamine-regulated transcript (CART) is an anorectic chemical in the brain. In the present study, we examined the hypothesis that CART may act in the central nervous system to alter gastric function. Food consumption, gastric acid secretion, and gastric emptying were measured after injection of CART into the cerebrospinal fluid in 24-h fasted Sprague Dawley rats. Central injection of CART inhibited food intake, gastric acid secretion, and gastric emptying. In contrast, ip injection of CART failed to inhibit gastric acid secretion and gastric emptying, suggesting that CART acts in the brain to suppress gastric acid secretion and gastric emptying. In the vagotomized animals, centrally administered CART did inhibit pentagastrin-stimulated gastric acid secretion. The CART-induced acid inhibition was also observed in rats treated with indomethacin, a cyclooxygenase inhibitor. In contrast, pretreatment with central administration of a CRF receptor antagonist, {alpha}-helical CRF9–41, completely blocked the central CART-induced inhibition of gastric acid secretion. All these results suggest that CART acts in the brain to inhibit gastric function via brain CRF system. The vagal pathway and the prostaglandin system are not involved in the acid inhibition.




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