首页> 外文期刊>Life sciences >THE SOMATOSTATIN RECEPTOR-ADENYLATE CYCLASE SYSTEM IN RAT PANCREATIC ACINAR MEMBRANES AFTER TEMPORARY PANCREATICOBILIARY DUCT LIGATION
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THE SOMATOSTATIN RECEPTOR-ADENYLATE CYCLASE SYSTEM IN RAT PANCREATIC ACINAR MEMBRANES AFTER TEMPORARY PANCREATICOBILIARY DUCT LIGATION

机译:临时胰胆管结扎术后大鼠胰腺PA膜中的生长抑素受体-腺苷酸环化系统

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The mechanism whereby somatostatin (SS) produces beneficial effects in established pancreatitis induced by pancreaticobiliary duct ligation (PBDL) is still not clear. The aim of the work was to evaluate the possibility of a direct action of SS on pancreatic acinar cells from rats with acute pancreatitis. For this purpose, we studied the SS-receptor-adenylate cyclase system in pancreatic acinar membranes from both, control rats and rats with experimentally induced acute pancreatitis. On the other hand, it has been reported that cholecystokinin (CCK) diminishes the number of SS receptors in pancreatic acinar cells. Proglumide, a CCK receptor antagonist reduces the severity of acute pancreatitis in the rat. Therefore, we have also examined the effect of proglumide on the somatostatinergic system in controls and rats with acute pancreatitis. Fourteen hours after PBDL, the SS receptors, the capacity of the SS analogue SMS 201-995 to inhibit forskolin-stimulated adenylate cyclase activity and PTX-catalyzed [P-32] ADP-ribosylation of the alpha(1) subunits of Gi proteins could not be detected in pancreatic acinar membranes. One month after reopening the closed pancreaticobiliary duct (PBD), the pancreas showed regeneration of acinar cells, and the above-mentioned parameters were significantly lower than in the control group. Two months after reopening the closed PBD, all these parameters had returned to control values. The administration of proglumide (20 mg/kg i.p.), a cholecystokinin receptor antagonist, accelerated pancreatic regeneration and approached all these parameters to control values one month after reopening the closed PBD. The present study suggests that the beneficial effects of SS on established pancreatitis induced by PBDL may not be due to a direct action of the peptide on pancreatic acinar cells at least at 14 hours after PBDL. In addition, these findings suggest that in established pancreatitis the effect of proglumide on the SS receptor-adenylate cyclase system could be due to its action on pancreatic regeneration. [References: 56]
机译:生长抑素(SS)在由胰胆管结扎(PBDL)诱发的已建立的胰腺炎中产生有益作用的机制仍不清楚。这项工作的目的是评估SS对急性胰腺炎大鼠胰腺腺泡细胞直接作用的可能性。为此,我们研究了对照大鼠和实验性急性胰腺炎大鼠的胰腺腺泡膜中的SS-受体-腺苷酸环化酶系统。另一方面,据报道胆囊收缩素(CCK)减少了胰腺腺泡细胞中SS受体的数量。丙谷胺(一种CCK受体拮抗剂)可降低大鼠急性胰腺炎的严重程度。因此,我们还检查了丙谷胺对对照组和急性胰腺炎大鼠生长抑素能系统的影响。 PBDL后的14小时,SS受体,SS类似物SMS 201-995抑制福斯科林刺激的腺苷酸环化酶活性和PTX催化Gi蛋白的alpha(1)亚基[P-32] ADP-核糖基化的能力可以在胰腺腺泡膜中未检测到。重新打开封闭的胰胆管(PBD)一个月后,胰腺显示出腺泡细胞的再生,上述参数明显低于对照组。重新打开封闭的PBD两个月后,所有这些参数已恢复为控制值。重新打开封闭的PBD后一个月,给予丙谷胺(20 mg / kg i.p.),一种胆囊收缩素受体拮抗剂,可加速胰腺再生,并使所有这些参数均达到控制值。本研究表明SS对PBDL引起的已建立的胰腺炎的有益作用可能不是由于肽至少在PBDL后14小时对胰腺腺泡细胞具有直接作用。此外,这些发现表明,在已确定的胰腺炎中,丙谷酰胺对SS受体-腺苷酸环化酶系统的作用可能是由于其对胰腺再生的作用。 [参考:56]

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