There has been no established theory about the LDH isozyme pattern in three parts (cortex, medulla, papilla) of Kidney with each different metabolism. This report involves the investigation of the LDH isozyme in three parts of human contracted kidney and rabbit kidney with the stenosis of renal artery. The results are as follows 1) Three parts of normal human kidney have different metabolic form LDH
1 and LDH
2 are predominant in cortex and medulla in other words H-type. On the other hand, LDH
4 and LDH
5 are predominant in papilla, that is M-type. In cortex and medulla of human contracted kidney, LDH
1 and LDH
2 bands reveal reduction. LDH
4 and LDH
5 bands increase relatively and are similar to the LDH Isozyme pattern in papilla. The O
2 consumption of human contracted kidney cortex and medulla, is reduced extremely and there is no change in papilla 2) The LDH Isozyme patterns in rabbit kidney with the prolonged stenosis and complete ligature of renal artery, are different from normal rabbit kidney. In cortex and medulla, the LDH Isozyme pattern is similar to the pattern in human contracted kidney. Because of high level of ishemia, prolonged ishemia and resulting degradation of the kidney tissue, the LDH Isozyme pattern changes from H-type to M-type. As a result of fitting for anaerobic metabolism, LDH
4, LDH
5 develop predominsnt figure and it seems that this phenomenon means the adaptations for keeping renal function as much as possible, and maintaining the constancy of body fluids.
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