Yakabi Koji, Kawashima Junichi, Kato Shingo
Department of Gastroentorlogy and Hepatology, Saitama Medical Center, Saitama Medical University, 1821 Kamoda Tsujido-machi, Kawagoe-city, Saitama 350-8550, Japan.
World J Gastroenterol. 2008 Nov 7;14(41):6334-8. doi: 10.3748/wjg.14.6334.
Ghrelin, a novel growth hormone-releasing peptide, was originally isolated from rat and human stomach. Ghrelin has been known to increase the secretion of growth hormone (GH), food intake, and body weight gain when administered peripherally or centrally. Ghrelin is also known to stimulate the gastric motility and the secretion of gastric acid. In the previous studies, the action of ghrelin on acid secretion was shown to be as strong as that of histamine and gastrin in in-vivo experiment. In the studies, the mechanism for the action of ghrelin was also investigated. It was shown that vagotomy completely inhibited the action of ghrelin on the secretion of gastric acid suggesting that vagal nerve is involved in the mechanism for the action of ghrelin on acid secretion. As famotidine did not inhibit ghrelin-induced acid secretion in the study by Masuda et al, they concluded that histamine was not involved in the action of ghrelin on acid secretion. However, we have shown that famotidine completely inhibited ghrelin-induced acid secretion and histidine decarboxylase (HDC) mRNA was increased in gastric mucosa by ghrelin injection which is inhibited by vagotomy Our results indicate that histamine is involved in the action of ghrelin on acid secretion. Furthermore synergistic action of gastrin and ghrelin on gastric acid secretion was shown. Although gastrin has important roles in postprandial secretion of gastric acid, ghrelin may be related to acid secretion during fasting period or at night. However, further studies are needed to elucidate the physiological role of ghrelin in acid secretion.
胃饥饿素是一种新型的生长激素释放肽,最初是从大鼠和人类的胃中分离出来的。已知胃饥饿素经外周或中枢给药时,会增加生长激素(GH)的分泌、食物摄入量和体重增加。胃饥饿素还能刺激胃蠕动和胃酸分泌。在之前的研究中,在体内实验中显示胃饥饿素对胃酸分泌的作用与组胺和胃泌素的作用一样强。在这些研究中,还对胃饥饿素的作用机制进行了研究。结果表明,迷走神经切断术完全抑制了胃饥饿素对胃酸分泌的作用,这表明迷走神经参与了胃饥饿素对胃酸分泌的作用机制。由于在增田等人的研究中,法莫替丁并未抑制胃饥饿素诱导的胃酸分泌,他们得出结论,组胺不参与胃饥饿素对胃酸分泌的作用。然而,我们已经表明,法莫替丁完全抑制了胃饥饿素诱导的胃酸分泌,并且通过注射胃饥饿素,胃黏膜中的组氨酸脱羧酶(HDC)mRNA增加,而迷走神经切断术可抑制这种增加。我们的结果表明,组胺参与了胃饥饿素对胃酸分泌的作用。此外,还显示了胃泌素和胃饥饿素对胃酸分泌的协同作用。虽然胃泌素在餐后胃酸分泌中起重要作用,但胃饥饿素可能与禁食期或夜间的胃酸分泌有关。然而,需要进一步研究来阐明胃饥饿素在胃酸分泌中的生理作用。