Hayashi T, Salata K, Kingman A, Notkins A L
Laboratory of Oral Medicine, National Institute of Dental Research, Bethesda, Maryland 20892.
Am J Pathol. 1988 Sep;132(3):503-11.
Since its discovery, lactic dehydrogenase virus (LDV) has remained unique as a model of long-term enzyme elevation due to impairment of enzyme clearance. The present study shows that mice inoculated with silica develop an increase in plasma lactate dehydrogenase (LDH) lasting for at least 6 months and that the enzyme elevation is due, at least in part, to impairment of clearance. The extent of the enzyme elevation is dependent on both the dose and route of silica administration and mice that had received both silica and LDV showed a more profound impairment of LDH clearance than mice that had received silica or LDV alone. Examination of the factors that regulate circulating enzyme levels in normal mice revealed that whereas there was no difference in resting enzyme levels among several inbred strains of mice (BALB/cAnN, NZBWF1/J,B10.D2/nSnN, and A/J mice), when mice were stressed by the administration of an enzyme load, certain inbred strains (BALB/cAnN) cleared the enzyme rapidly and others (B10.D2/nSnN) cleared the enzyme slowly. Moreover, in B10.D2/nSnN mice, enzyme clearance was age-related. When different strains of mice were infected with LDV, LDH levels were substantially higher in the circulation of slow enzyme clearers as compared to rapid enzyme clearers. It is concluded that both environmental and genetic factors influence the clearance of LDH and that impairment of enzyme clearance may be a more important factor than previously suspected in regulating enzyme levels in disease states.
自乳酸脱氢酶病毒(LDV)被发现以来,它作为因酶清除受损导致长期酶升高的模型一直独具特色。本研究表明,接种二氧化硅的小鼠血浆乳酸脱氢酶(LDH)升高持续至少6个月,且酶升高至少部分归因于清除受损。酶升高的程度取决于二氧化硅的给药剂量和途径,同时接受二氧化硅和LDV的小鼠比单独接受二氧化硅或LDV的小鼠表现出更严重的LDH清除受损。对正常小鼠中调节循环酶水平的因素进行研究发现,虽然几种近交系小鼠(BALB/cAnN、NZBWF1/J、B10.D2/nSnN和A/J小鼠)的静息酶水平没有差异,但当给小鼠施加酶负荷使其应激时,某些近交系(BALB/cAnN)能迅速清除酶,而其他近交系(B10.D2/nSnN)清除酶的速度较慢。此外,在B10.D2/nSnN小鼠中,酶清除与年龄相关。当不同品系的小鼠感染LDV时,与酶清除速度快的小鼠相比,酶清除速度慢的小鼠循环中的LDH水平显著更高。得出的结论是,环境和遗传因素均影响LDH的清除,且在疾病状态下调节酶水平方面,酶清除受损可能是一个比之前怀疑的更为重要的因素。