Objective. To study the characteristics of changes of LDH enzyme patterns of mice under slight hypoxia.Methods. Mice treated with artificial hypoxia, various tissues were made for the test of LDH enzymatic activity by...Objective. To study the characteristics of changes of LDH enzyme patterns of mice under slight hypoxia.Methods. Mice treated with artificial hypoxia, various tissues were made for the test of LDH enzymatic activity by the specific staining technique. LDH (1 -5) relative percentage enzymatic activity (RPEA) were measured with CS-910 dual-wavelength thin layer chromatography scanner.Results. The RPEA of LDH isozymes of various tissues after slight hypoxia shifted to the isozymes LDH1 and LDH2, whose principal subunits are H subunits, and the RPEA of LDH,(H4), LDH2(H3M) increased, while RPEA of LDH5(M4) in various tissues decreased prominently except the cardiac muscle, and that of LDH4(HM3) decreased as well. After polyacrylamide gel electrophoresis (PAGE) of the hypoxia treated cardiac muscle specimen was made, activity subbands originated regularly in the isozyme patterns of LDH, with the regularity of LDH1 (0 subband), LDH2 (0-1 subbands), LDH3 (0-2 subbands), LDH4 (1-3 subbands), LDH5 (2-4 subbands). After adding appropriate amount of NAD+ to the hypoxia treated cardiac muscle specimen, PAGE showed the subbands of four isozymes (LDH2-LDH5) reduced or even totally disappeared in the isozyme patterns.Conclusions. The negative feedback regulation of coenzymization and decoenzymization of LDH isozymes is one of the mouse stress responses to slight hypoxia.展开更多
LDH-A_4,B_4,and C_4 were isolated and purified from Ctenopharyngodon idellus tissues by means ofaffinity chromatography.The purity,amino acid content and kinetics were analyzed.The anti-LDH-A_4,B_4,and C_4 antibodies ...LDH-A_4,B_4,and C_4 were isolated and purified from Ctenopharyngodon idellus tissues by means ofaffinity chromatography.The purity,amino acid content and kinetics were analyzed.The anti-LDH-A_4,B_4,and C_4 antibodies were prepared from rabbit sensitized by LDH-A_4,B_4,and C_4respectively.The LDH patterns of some freshwater fish and marine fish were identified by theantigen-antibody precipitation reaction.The homology between LDH isozyme molecules fromdifferent sources and the immunological homology of different LDH isozymes were discussed.展开更多
文摘Objective. To study the characteristics of changes of LDH enzyme patterns of mice under slight hypoxia.Methods. Mice treated with artificial hypoxia, various tissues were made for the test of LDH enzymatic activity by the specific staining technique. LDH (1 -5) relative percentage enzymatic activity (RPEA) were measured with CS-910 dual-wavelength thin layer chromatography scanner.Results. The RPEA of LDH isozymes of various tissues after slight hypoxia shifted to the isozymes LDH1 and LDH2, whose principal subunits are H subunits, and the RPEA of LDH,(H4), LDH2(H3M) increased, while RPEA of LDH5(M4) in various tissues decreased prominently except the cardiac muscle, and that of LDH4(HM3) decreased as well. After polyacrylamide gel electrophoresis (PAGE) of the hypoxia treated cardiac muscle specimen was made, activity subbands originated regularly in the isozyme patterns of LDH, with the regularity of LDH1 (0 subband), LDH2 (0-1 subbands), LDH3 (0-2 subbands), LDH4 (1-3 subbands), LDH5 (2-4 subbands). After adding appropriate amount of NAD+ to the hypoxia treated cardiac muscle specimen, PAGE showed the subbands of four isozymes (LDH2-LDH5) reduced or even totally disappeared in the isozyme patterns.Conclusions. The negative feedback regulation of coenzymization and decoenzymization of LDH isozymes is one of the mouse stress responses to slight hypoxia.
文摘LDH-A_4,B_4,and C_4 were isolated and purified from Ctenopharyngodon idellus tissues by means ofaffinity chromatography.The purity,amino acid content and kinetics were analyzed.The anti-LDH-A_4,B_4,and C_4 antibodies were prepared from rabbit sensitized by LDH-A_4,B_4,and C_4respectively.The LDH patterns of some freshwater fish and marine fish were identified by theantigen-antibody precipitation reaction.The homology between LDH isozyme molecules fromdifferent sources and the immunological homology of different LDH isozymes were discussed.
