Jivegård L, Thune A, Svanvik J
Department of Surgery I, Gothenburg University, Sweden.
Acta Physiol Scand. 1988 Apr;132(4):549-55. doi: 10.1111/j.1748-1716.1988.tb08364.x.
Gallbladder mucosal net fluid transport and motility were measured in vivo by a continuous perfusion technique in the anaesthetized cat. Prostaglandin E2, administered to the perfused gallbladder lumen, caused a contraction decreasing gallbladder volume capacity, and induced a secretory response by the mucosa. These effects by prostaglandin E2 were abolished by the nerve-blocking agent tetrodotoxin (administered close intraarterially) and somatostatin (administered intravenously), but not by intravenous hexamethonium. Atropine (administered intravenously) reduced the order of magnitude of the gallbladder contraction in response to prostaglandin E2 but did not affect the secretory response by the mucosa. Neither of these drugs significantly affected gallbladder volume capacity or mucosal fluid transport during basal conditions. Tetrodotoxin did not abolish the gallbladder responses to intravenous cholecystokinin or vasoactive intestinal peptide, peptides known to act directly upon smooth muscle and epithelial cell receptors, respectively. It is suggested that prostaglandin E2 affects gallbladder function in vivo mainly by activation of postganglionic non-cholinergic intramural nerve cells.
在麻醉猫身上,采用连续灌注技术对胆囊黏膜净液体转运和运动能力进行了体内测量。向灌注的胆囊腔内注入前列腺素E2,可引起胆囊收缩,胆囊容积减小,并诱导黏膜产生分泌反应。前列腺素E2的这些作用可被神经阻滞剂河豚毒素(动脉内近距离给药)和生长抑素(静脉给药)消除,但不能被静脉注射六甲铵消除。阿托品(静脉给药)降低了胆囊对前列腺素E2反应的收缩幅度,但不影响黏膜的分泌反应。在基础状态下,这些药物均未显著影响胆囊容积或黏膜液体转运。河豚毒素并未消除胆囊对静脉注射胆囊收缩素或血管活性肠肽的反应,已知这两种肽分别直接作用于平滑肌和上皮细胞受体。提示前列腺素E2在体内主要通过激活节后非胆碱能壁内神经细胞来影响胆囊功能。