Poli E, Coruzzi G, Bertaccini G
Institute of Pharmacology, University of Parma, Italy.
Life Sci. 1991;48(13):PL63-8. doi: 10.1016/0024-3205(91)90531-f.
The effect of selective histamine H3-receptor agonists and antagonists on the acetylcholine release from peripheral nerves was evaluated in the guinea pig longitudinal muscle-myenteric plexus preparations, preloaded with (3H)choline. In the presence of H1 and H2 blockade, histamine (10(-7)-10(-4) M) and (R)-alpha-methylhistamine (10(-8)-10(-6) M) inhibited the electrically-evoked acetylcholine release, being (R)-alpha-methylhistamine more active than histamine, but behaving as a partial agonist. The effect of histamine was completely reversed by selective H3-blocking drugs, thioperamide and impromidine, while only submaximal doses of (R)-alpha-methylhistamine were antagonized. Furthermore, thioperamide and impromidine enhanced the electrically-evoked acetylcholine release. On the contrary, the new H3-blocker, HST-7, was found substantially ineffective, both as histamine antagonist and as acetylcholine overflow enhancer. These data suggest that histamine exerts an inhibitory control on the acetylcholine release from intestinal cholinergic nerves through the activation of H3 receptors.
在预先加载了(3H)胆碱的豚鼠纵行肌-肠肌丛标本中,评估了选择性组胺H3受体激动剂和拮抗剂对周围神经乙酰胆碱释放的影响。在存在H1和H2受体阻断的情况下,组胺(10^(-7)-10^(-4) M)和(R)-α-甲基组胺(10^(-8)-10^(-6) M)抑制电诱发的乙酰胆碱释放,(R)-α-甲基组胺比组胺更具活性,但表现为部分激动剂。组胺的作用被选择性H3阻断药物硫代哌啶和英普咪定完全逆转,而只有次最大剂量的(R)-α-甲基组胺被拮抗。此外,硫代哌啶和英普咪定增强了电诱发的乙酰胆碱释放。相反,新型H3阻断剂HST-7被发现基本上无效,既不能作为组胺拮抗剂,也不能作为乙酰胆碱溢出增强剂。这些数据表明,组胺通过激活H3受体对肠胆碱能神经的乙酰胆碱释放发挥抑制性控制作用。