Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/133949
DC FieldValue
dc.titleThe effects of an interferon inducer, polyriboinosinic polyribocytidylic acid on cytochrome P-450 dependent hepatic progesterone metabolism
dc.contributor.authorWong, J.Y.Y.
dc.contributor.authorLee, E.J.D.
dc.contributor.authorMoochhala, S.M.
dc.date.accessioned2016-12-20T08:41:49Z
dc.date.available2016-12-20T08:41:49Z
dc.date.issued1993
dc.identifier.citationWong, J.Y.Y., Lee, E.J.D., Moochhala, S.M. (1993). The effects of an interferon inducer, polyriboinosinic polyribocytidylic acid on cytochrome P-450 dependent hepatic progesterone metabolism. Life Sciences 53 (25) : 1893-1901. ScholarBank@NUS Repository.
dc.identifier.issn00243205
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/133949
dc.description.abstractA time course study on the effects of an interferon inducing agent, polyriboinosinic polyribocytidylic acid (poly rIrC) on the hepatic cytochrome P-450 dependent progesterone metabolism was performed. Administration of a single dose of poly rIrC (10 mg/kg i.p.) to adult male Wistar rats caused a time dependent effect on liver weight, microsomal protein and total cytochrome P-450 levels, as well as the 16α and 6β hydroxylation of progesterone. The response was multiphasic, with a maximal depression of both hydroxylase activity 48 hours post-injection, followed by enhanced activity at 72 hours and subsequent return to control activity twenty-four hours later. A second less dramatic rise in the activities followed, bringing the 16α and 6β hydroxylase activity to 159% and 141% of their respective control values by 336 hours, at which point of time, the trend appeared to be still on the rise. The enhanced activity at 72 hours was preceded by an increase in serum cortisol and corticosterone levels, the ability of which to enhance the activity of 6β hydroxylation of steroids may partly explain the phenomenon. © 1993.
dc.typeArticle
dc.contributor.departmentPHARMACOLOGY
dc.description.sourcetitleLife Sciences
dc.description.volume53
dc.description.issue25
dc.description.page1893-1901
dc.description.codenLIFSA
dc.identifier.isiutNOT_IN_WOS
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