Schusdziarra V, Rewes B, Lenz N, Maier V, Pfeiffer E F
Regul Pept. 1983 Aug;6(4):355-61. doi: 10.1016/0167-0115(83)90264-1.
Previously, we have demonstrated the effects of exogenously administered opiates on somatostatin release in dogs and therefore the present study was designed to determine the effect of endogenous opiates via naloxone-induced opiate receptor blockade on somatostatin release. Additionally, plasma insulin and pancreatic polypeptide (PP) levels were determined in response to intragastrically instilled protein, carbohydrate and fat test meals in a group of eight conscious dogs. To all test meals either naloxone (4 mg) or saline was added. The rise of plasma somatostatin levels in response to liver extract, sucrose and fat was attenuated significantly by naloxone. Naloxone had no effect on the rise of postprandial plasma insulin and PP levels. The present data demonstrate that endogenous opiates have a stimulatory effect on postprandial somatostatin release in dogs which indicates a tight interaction that might be of relevance for nutrient homeostasis.
此前,我们已经证明了外源性给予阿片类药物对犬生长抑素释放的影响,因此本研究旨在通过纳洛酮诱导的阿片受体阻断来确定内源性阿片类药物对生长抑素释放的影响。此外,在一组8只清醒犬中,测定了胃内灌注蛋白质、碳水化合物和脂肪试验餐时血浆胰岛素和胰多肽(PP)水平。向所有试验餐中加入纳洛酮(4毫克)或生理盐水。纳洛酮显著减弱了肝脏提取物、蔗糖和脂肪引起的血浆生长抑素水平的升高。纳洛酮对餐后血浆胰岛素和PP水平的升高没有影响。目前的数据表明,内源性阿片类药物对犬餐后生长抑素释放具有刺激作用,这表明存在一种紧密的相互作用,可能与营养稳态相关。