Studies of Y and Z, two hepatic cytoplasmic organic anion-binding proteins: effect of drugs, chemicals, hormones, and cholestasis

Humberto Reyes; A. Jonathan Levi; Zenaida Gatmaitan; Irwin M. Arias

doi:10.1172/JCI106721

Studies of Y and Z, two hepatic cytoplasmic organic anion-binding proteins: effect of drugs, chemicals, hormones, and cholestasis

Humberto Reyes, A. Jonathan Levi, Zenaida Gatmaitan, and Irwin M. Arias

Published November 1, 1971 - More info

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Abstract

The process by which various anions, including bilirubin and several dyes, drugs, hormones and their metabolites, are transferred from plasma into the liver cell is poorly understood. Two hepatic cytoplasmic proteins, Y and Z, that bind various organic anions in vivo and in vitro have been postulated to be involved in this process.

The concentration of Y, the major organic anion-binding protein, increases in rat liver after administration of phenobarbital in association with enhanced organic anion transfer from plasma into liver as determined by initial plasma disappearance rate (K₁) and hepatic dye content for sulfobromophthalein (BSP) and indocyanine green (ICG), as well as increased relative hepatic storage of BSP. Acute bile duct ligation failed to alter plasma disappearance or hepatic content of BSP in normal or phenobarbital-treated rats.

Other drugs and chemicals which cause proliferation of hepatic smooth endoplasmic reticulum and enhancement of drug metabolism, such as allylisopropylacetamide, dieldrin, DDT, 3-methylcholanthrene, and benzpyrene increased Y and BSP K₁ and, where studied, hepatic BSP content. Alcohol feeding had no effect on Y, Z, or K₁ for BSP.

Hypophysectomy and thyroidectomy increased Y but decreased K₁ and, where studied, hepatic content of BSP. Of several hormones studied, only thyroxine restored Y and K₁ to normal in hypophysectomized or thyroidectomized rats. Mice with congenital pituitary insufficiency also manifested increased Y which returned to normal after thyroxine administration. In hormone-deficient rats and mice, phenobarbital administration produced a further increase in Y suggesting that different mechanisms may be responsible for the change in Y resulting from drug administration and hormonal deprivation. Thyroxine, testosterone, or hydrocortisone did not alter BSP K₁ or Y in normal rats.

Cholestasis produced by ethinyl estradiol administration or biliary obstruction reduced Y, Z, BSP K₁ and hepatic BSP content.

These results support the hypothesis that Y and Z are involved in the transfer of BSP, ICG, and possibly other organic anions from plasma into the liver. The concentration of Y increased after administration of various drugs and chemicals as well as in thyroid deficiency. Thyroid hormone appears to be important in regulation of the intracellular concentration of Y. Because thyroid deficiency increased Y but decreased BSP K₁ and hepatic BSP content, other factors beside Y and Z influence hepatic organic anion uptake.