Albinus M, Sewing K F
Agents Actions. 1981 May;11(3):223-7. doi: 10.1007/BF01967618.
3H-Histamine binding, uptake and metabolism were investigated in intact isolated and enriched parietal cells from the dog and guinea pig. Histamine uptake was sodium dependent and followed by intracellular metabolism. The only metabolite that was detected and extracted from cytosol has been identified by TLC to N tau-methylhistamine. The histamine N-methyltransferase activity appeared to be sodium dependent and was inhibited by mepyramine and chlorpromazine, and also by higher concentrations (10(-4)--10(-3) mol/l) of cimetidine. Two blockers of the sodium channel, amiloride an aminoguanidine, also reduced the enzyme activity by an as yet unknown mechanism.
在从狗和豚鼠分离并富集的完整壁细胞中研究了³H-组胺的结合、摄取和代谢。组胺摄取依赖于钠,并伴有细胞内代谢。通过薄层层析法从细胞溶质中检测并提取到的唯一代谢产物已被鉴定为N-τ-甲基组胺。组胺N-甲基转移酶活性似乎依赖于钠,并受到美吡拉敏、氯丙嗪以及更高浓度(10⁻⁴ - 10⁻³mol/L)西咪替丁的抑制。两种钠通道阻滞剂,即氨氯吡脒和氨基胍,也通过一种尚不清楚的机制降低了该酶的活性。