Bryce G F, Jacoby J H
Eur J Pharmacol. 1979 Mar 15;54(4):349-57. doi: 10.1016/0014-2999(79)90064-5.
The administration of cyproheptadine (25 mg/kg; i.p.) resulted in an increase of plasma insulin and glucagon (measured using 30 K antibody) 30, 60 and 120 min after injection to fasted rats. This dose of cyproheptadine also induced a hyperglycemia whereas a lower dose (5 mg/kg; i.p.), which did not alter plasma hormone levels, was associated with a hypoglycemia. Fed rats showed a reduction of plasma insulin with a similar elevation of blood glucose after cyproheptadine. Administration of an exogenous load of arginine resulted in increases of plasma insulin and glucagon of a greater magnitude than induced by cyproheptadine, however, cyproheptadine pretreatment (25 mg/kg) completely suppressed the pancreatic response to the amino acid, resulting in blood hormone levels similar to values seen after cyproheptadine administered alone. Cyproheptadine pretreatment also prevented the hyperinsulinemia and hypoglucagonemia resulting from glucose loading. alpha-Adrenergic receptor blockade (with phentolamine), beta adrenergic receptor blockade (with propranolol) and adrenodemedullation did not alter pancreatic responsiveness to the drug.
给禁食大鼠腹腔注射赛庚啶(25毫克/千克)后30、60和120分钟,血浆胰岛素和胰高血糖素(使用30K抗体测量)水平升高。该剂量的赛庚啶还诱发了高血糖,而较低剂量(5毫克/千克;腹腔注射)未改变血浆激素水平,却导致了低血糖。喂食大鼠在注射赛庚啶后血浆胰岛素降低,血糖有类似程度的升高。给予外源性精氨酸负荷后,血浆胰岛素和胰高血糖素的升高幅度大于赛庚啶诱导的幅度,然而,赛庚啶预处理(25毫克/千克)完全抑制了胰腺对氨基酸的反应,导致血液激素水平与单独注射赛庚啶后的数值相似。赛庚啶预处理还可预防葡萄糖负荷引起的高胰岛素血症和低胰高血糖素血症。α-肾上腺素能受体阻断(使用酚妥拉明)、β-肾上腺素能受体阻断(使用普萘洛尔)和肾上腺髓质切除均未改变胰腺对该药物的反应性。