Poli E, Coruzzi G, Bertaccini G
Institute of Pharmacology, University of Parma, Italy.
Agents Actions. 1988 Apr;23(3-4):241-3. doi: 10.1007/BF02142552.
Histamine was tested on the guinea pig isolated urinary bladder to determine both the direct effect on the muscle and the influence on the contractions induced by field stimulation. Histamine (10(-7)-10(-3) M) caused contraction of the bladder and enhancement of the atropine-resistant response to field stimulation. These effects were sensitive to the H1-receptor antagonist pyrilamine (pA2 = 8.55 and 7.07, respectively). The H2-antagonists cimetidine and famotidine were ineffective on both parameters. It is concluded that predominantly H1-receptors are present in the guinea pig urinary bladder and that they are localized both on the muscle and on non-cholinergic nerve terminals. The significant difference between the pA2 values for pyrilamine is likely to suggest a heterogeneity in the H1-receptor population.
对豚鼠离体膀胱进行组胺测试,以确定其对肌肉的直接作用以及对场刺激诱导收缩的影响。组胺(10⁻⁷ - 10⁻³ M)可引起膀胱收缩,并增强对场刺激的阿托品抵抗反应。这些作用对H1受体拮抗剂吡拉明敏感(pA2分别为8.55和7.07)。H2拮抗剂西咪替丁和法莫替丁对这两个参数均无效。结论是豚鼠膀胱中主要存在H1受体,且它们定位于肌肉和非胆碱能神经末梢。吡拉明pA2值之间的显著差异可能表明H1受体群体存在异质性。