Schirmer B D, Kortz W J, Miller R J, Jones R S
J Surg Res. 1985 Sep;39(3):237-45. doi: 10.1016/0022-4804(85)90148-9.
Previous experiments have demonstrated the cholestatic effects of somatostatin administration in several animal species. These effects were confirmed in the rat. Nine pairs of intact awake rats received intravenous sodium taurocholate (23 mg hr-1) to stabilize bile flow, and half were later given somatostatin at doses of 185 micrograms hr-1. After 1 hr of somatostatin the experimental group showed a significant decrease in bile flow compared to the control group. Cholestasis reversed when somatostatin infusion was stopped. An in situ isolated perfused rat liver technique was used to assess the direct effects of somatostatin on biliary flow. In 10 pairs of rat livers, after achieving stable bile flow, half of those perfused (the "experimentals") received continuous (370 micrograms hr-1) somatostatin infusion, while the controls received saline. The percentage change in bile flow from baseline in the somatostatin group was not significantly different from that in controls for any test period. Bile analysis revealed no significant differences between groups for cholesterol, phospholipid, or bile salt concentrations or outputs. These data suggest that somatostatin inhibits bile secretion by some mechanism other than direct inhibition of bile secretory mechanisms.
先前的实验已证明,在几种动物物种中给予生长抑素会产生胆汁淤积作用。这些作用在大鼠中得到了证实。九对完整清醒的大鼠接受静脉注射牛磺胆酸钠(23毫克/小时)以稳定胆汁流量,其中一半大鼠随后以185微克/小时的剂量给予生长抑素。在给予生长抑素1小时后,与对照组相比,实验组的胆汁流量显著降低。当停止输注生长抑素时,胆汁淤积得到逆转。采用原位离体灌注大鼠肝脏技术来评估生长抑素对胆汁流动的直接作用。在10对大鼠肝脏中,在实现稳定胆汁流量后,一半灌注肝脏(“实验组”)接受持续(370微克/小时)的生长抑素输注,而对照组接受生理盐水。在任何测试期间,生长抑素组胆汁流量相对于基线的百分比变化与对照组相比均无显著差异。胆汁分析显示,两组之间的胆固醇、磷脂或胆汁盐浓度及输出量均无显著差异。这些数据表明,生长抑素通过直接抑制胆汁分泌机制以外的某种机制抑制胆汁分泌。