Literature DB >> 1673385

Chronic stress impairs oxidative metabolism and hepatic excretion of model xenobiotic substrates in the rat.

G M Pollack1, J L Browne, J Marton, L J Haberer.   

Abstract

Traumatic injury to both hard and soft tissue has been associated with a decrease in the rate of hepatic drug metabolism. The mechanism(s) underlying this phenomenon have yet to be determined, but may involve substances released from damaged tissues or activation of the adrenocortical axis secondary to stress. To determine whether a generalized stress response is involved in the trauma-induced perturbations of xenobiotic metabolism, rats were exposed to atraumatic stress for a period of 21 days prior to determining the disposition of antipyrine (an in vivo marker for the hepatic mixed-function oxidase system) and indocyanine green (a tricarbocyanine dye often used as an in vivo marker of active hepatic uptake). Exposure to stress resulted in a significant decrease in the systemic clearance of antipyrine, suggesting a stress-induced inhibition of hepatic oxidation. In addition, the stressed animals evidenced a decreased rate of uptake of indocyanine green by the liver, an apparent decrease in the storage of the dye within the liver, and a decreased hepatic clearance of indocyanine green (presumably due to a decrease in the KM for biliary transport). These observations suggest that atraumatic stress affects several processes involved in the hepatobiliary disposition of xenobiotics.

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Year:  1991        PMID: 1673385

Source DB:  PubMed          Journal:  Drug Metab Dispos        ISSN: 0090-9556            Impact factor:   3.922


  7 in total

1.  Dynamics of hepatic gene expression profile in a rat cecal ligation and puncture model.

Authors:  Qian Yang; John S A Mattick; Mehmet A Orman; Tung T Nguyen; Marianthi G Ierapetritou; Francois Berthiaume; Ioannis P Androulakis
Journal:  J Surg Res       Date:  2011-12-15       Impact factor: 2.192

2.  Anxiolytic effects of phosphodiesterase-2 inhibitors associated with increased cGMP signaling.

Authors:  Anbrin Masood; Ying Huang; Hassan Hajjhussein; Lan Xiao; Hao Li; Wei Wang; Adel Hamza; Chang-Guo Zhan; James M O'Donnell
Journal:  J Pharmacol Exp Ther       Date:  2009-08-14       Impact factor: 4.030

3.  Changes in serum levels of quinolones in rats under the influence of experimental trauma.

Authors:  A Trichilis; C Tesserommatis; D Varonos
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2000 Apr-Jun       Impact factor: 2.569

4.  The role of stress in the regulation of drug metabolizing enzymes in mice.

Authors:  M Konstandi; M Marselos; A M Radon-Camus; E Johnson; M A Lang
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1998 Oct-Dec       Impact factor: 2.569

5.  Evidence of alpha2-adrenoceptor involvement in B[alpha]P induction processes of drug-metabolizing enzymes: the effect of stress.

Authors:  M Konstandi; D Kostakis; E Johnson; M A Lang; M Marselos
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1998 Oct-Dec       Impact factor: 2.569

6.  Mice do not habituate to metabolism cage housing--a three week study of male BALB/c mice.

Authors:  Otto Kalliokoski; Kirsten R Jacobsen; Huda S Darusman; Trine Henriksen; Allan Weimann; Henrik E Poulsen; Jann Hau; Klas S P Abelson
Journal:  PLoS One       Date:  2013-03-07       Impact factor: 3.240

Review 7.  Should oral gavage be abandoned in toxicity testing of endocrine disruptors?

Authors:  Laura N Vandenberg; Wade V Welshons; Frederick S Vom Saal; Pierre-Louis Toutain; John Peterson Myers
Journal:  Environ Health       Date:  2014-06-25       Impact factor: 5.984

  7 in total

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