Udupa S L
Department of Biochemistry, Kasturba Medical College, Manipal, India.
Indian J Exp Biol. 1995 Apr;33(4):278-80.
Isoniazid, an antitubercular drug, is known to be a potent inhibitor of monoamine oxidases. Effects of this drug, on lysyl oxidase (also a monoamine oxidase) and other wound healing parameters were studied in albino rats, in presence and absence of pyridoxal phosphate, using a dead space wound model. Tensile strength, collagen and glycosaminoglycan contents as well as lysyl oxidase activity were estimated in the granuloma tissue harvested from 10 day old dead space wounds. Isoniazid inhibited lysyl oxidase activity and a decrease in tensile strength as well as collagen content were observed. The effects were reversed on administration of a stoichiometric amount of pyridoxal phosphate. Hexosamine level was increased and hexuronic acid level decreased in the drug treated animals. Therefore, isoniazid may decrease the mechanical strength of collagen by inhibiting lysyl oxidase, by competiting for its obligatory cofactor pyridoxal phosphate, as well as by interfering in electrostatic interactions between collagen and the ground substance.
异烟肼是一种抗结核药物,已知是单胺氧化酶的强效抑制剂。使用死腔伤口模型,在有和没有磷酸吡哆醛的情况下,研究了该药物对白化病大鼠赖氨酰氧化酶(也是一种单胺氧化酶)和其他伤口愈合参数的影响。从10日龄死腔伤口收获的肉芽肿组织中估计了抗张强度、胶原蛋白和糖胺聚糖含量以及赖氨酰氧化酶活性。异烟肼抑制赖氨酰氧化酶活性,并观察到抗张强度和胶原蛋白含量降低。给予化学计量的磷酸吡哆醛后,这些影响得到逆转。药物治疗的动物中己糖胺水平升高,己糖醛酸水平降低。因此,异烟肼可能通过抑制赖氨酰氧化酶、竞争其必需辅因子磷酸吡哆醛以及干扰胶原蛋白与基质之间的静电相互作用来降低胶原蛋白的机械强度。