Sex differences in the control of glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase. Interaction of estrogen, testosterone and insulin in the regulation of enzyme levels in vivo and in cultured hepatocytes
- PMID: 3311073
- DOI: 10.1515/bchm3.1987.368.2.955
Sex differences in the control of glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase. Interaction of estrogen, testosterone and insulin in the regulation of enzyme levels in vivo and in cultured hepatocytes
Abstract
Control of the activities of glucose-6-phosphate dehydrogenase, 6-phosphogluconate dehydrogenase, and malate dehydrogenase was investigated in intact rats and in hepatocyte cultures. 1) Adult females had 2-fold greater activities of hepatic glucose-6-phosphate- and 6-phosphogluconate dehydrogenases than adult males, but similar activities of malate dehydrogenase. Castrated males showed decreased activities of all three enzymes in comparison to age- and weight-matched intact controls. In starved animals the activities of all three enzymes decreased significantly. After refeeding with nonpurified diet the activities returned to the prestarved levels in females, but increased to clearly higher values in intact and castrated males. 2) Estrogen levels were in the same range in immature and adult male and female rats. Testosterone levels were highest in adult males, clearly lower in adult females (1/8) and immature males (1/8), still lower in immature females (1/15) and lowest in castrated males (1/40). A simple correlation of the sex differences in these hormone levels to sex differences in glucose-6-phosphate- and 6-phosphogluconate dehydrogenase activities was not apparent. 3) In serum-free, dexamethasone-supplemented 48-h cultures of hepatocytes from both male and female rats the basal activities of glucose-6-phosphate dehydrogenase were the same; they were increased 2-3 fold by insulin alone, 1.5 fold by estrogen alone and 4-5 fold by insulin plus estrogen. Apparently sex differences did not persist in 48-h cell cultures. 4) In 48-h cultures of male hepatocytes, then used as the experimental model, insulin alone increased the activity not only of glucose-6-phosphate dehydrogenase but also of 6-phosphogluconate and malate dehydrogenases.(ABSTRACT TRUNCATED AT 250 WORDS)
Similar articles
-
Gender-linked differences in dietary induction of hepatic glucose-6 phosphate dehydrogenase, 6-phosphogluconate dehydrogenase and malic enzyme in the rat.J Nutr. 1986 Aug;116(8):1547-54. doi: 10.1093/jn/116.8.1547. J Nutr. 1986. PMID: 3761010
-
Dietary induction of hepatic glucose-6-phosphate dehydrogenase, 6-phosphogluconate dehydrogenase, and malic enzyme in lean and obese female Zucker rats.Proc Soc Exp Biol Med. 1987 Mar;184(3):278-84. doi: 10.3181/00379727-184-42479. Proc Soc Exp Biol Med. 1987. PMID: 3823105
-
Regulation of liver and brain hexose monophosphate dehydrogenases by insulin and dietary intake in the female rat.Mol Cell Biochem. 1986 May;70(2):169-75. doi: 10.1007/BF00229431. Mol Cell Biochem. 1986. PMID: 3523210
-
Dehydrogenases of the pentose phosphate pathway in rat liver peroxisomes.Eur J Biochem. 1989 Jul 15;183(1):75-82. doi: 10.1111/j.1432-1033.1989.tb14898.x. Eur J Biochem. 1989. PMID: 2753047
-
Estrogen, testosterone, and gender differences.Endocrine. 2005 Aug;27(3):259-67. doi: 10.1385/ENDO:27:3:259. Endocrine. 2005. PMID: 16230782 Review.
Cited by
-
Sulfation and glucuronidation of acetaminophen by cultured hepatocytes reproducing in vivo sex-differences in conjugation on Matrigel and type 1 collagen.In Vitro Cell Dev Biol. 1991 Dec;27A(12):953-60. doi: 10.1007/BF02631123. In Vitro Cell Dev Biol. 1991. PMID: 1757400
-
Changes in activity and intra-acinar distribution of glucose-6-phosphate dehydrogenase and malic enzyme during pregnancy in rat liver.Histochemistry. 1991;95(4):365-71. doi: 10.1007/BF00266964. Histochemistry. 1991. PMID: 2022487
-
Enzyme activity patterns of phosphoenolpyruvate carboxykinase, pyruvate kinase, glucose-6-phosphate-dehydrogenase and malic enzyme in human liver.Histochemistry. 1990;93(4):409-15. doi: 10.1007/BF00315859. Histochemistry. 1990. PMID: 2323955
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical