INHIBITION OF HISTAMINE N-METHYLTRANSFERASE (HNMT) INVITRO BY NEUROMUSCULAR RELAXANTS

被引:16
作者
FUTO, J [1 ]
KUPFERBERG, JP [1 ]
MOSS, J [1 ]
机构
[1] UNIV CHICAGO,DEPT ANESTHESIA & CRIT CARE,5841 MARYLAND AVE,BOX 428,CHICAGO,IL 60637
关键词
D O I
10.1016/0006-2952(90)90045-M
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
There have been reports of hypotension and flushing following vecuronium administration. The etiology of these symptoms, which are similar to those of histamine release, is not clear. The steroidal neuromuscular relaxants (NMRs), unlike muscle relaxants structurally similar to curare, have been shown not to cause histamine release after the administration of typical clinical doses. Histamine levels in plasma reflect a balance between release and catabolism. In humans, histamine N-methyl-transferase (HNMT) is the enzyme primarily degrading for histamine. Therefore, we performed in vitro kinetic studies of purified HNMT to determine the effects of the steroidal and curare-like NMRs and also of gallamine on histamine catabolism. We demonstrated that all NMRs tested were inhibitors of HNMT in vitro. The inhibition was competitive with respect to the cosubstrate S-adenosyl-L-[3H-methyl] methionine, and noncompetitive with respect to histamine. The rank order of inhibition was vecuronium>pancuronium>gallamine>d-tubocurarine > metocurine > atracurium > pipecuronium, with Ki values ranging from 1.2 to 44.8 μM. Our data suggest that HNMT-based radioenzymatic assays for histamine should be susceptible to inhibition by concurrent use of NMRs, particularly vecuronium. © 1990.
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页码:415 / 420
页数:6
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