Expression of cyclooxygenase enzymes in rat hypothalamo-pituitary-adrenal axis: effects of endotoxin and glucocorticoids
- PMID: 11887933
- DOI: 10.1385/ENDO:16:2:123
Expression of cyclooxygenase enzymes in rat hypothalamo-pituitary-adrenal axis: effects of endotoxin and glucocorticoids
Abstract
Prostaglandins play a key role in mediating the hypothalamo-pituitary-adrenocortical (HPA) responses to immune insults. This study aimed to provide some insight into the relative contributions of the constitutive and inducible forms of cyclooxygenase (COX-1 and COX-2) to the generation of these prostanoids by examining the effects of (1) endotoxin treatment on the expression of COX-1 and COX-2 mRNAs in the various components of the HPA axis in control and glucocorticoid pretreated rats, and (2) selective inhibition of COX-2 on the production of corticosterone by adrenal tissue in vitro. Endotoxin caused a marked rise in COX-2 mRNA in the adrenal gland that was evident 3 and 6 h after the injection and was prevented by pretreatment with dexamethasone. It also induced a modest increase in COX-2 mRNA in the hypothalamus but not in the hippocampus or anterior pituitary gland. By contrast, COX-1 mRNA was largely unaffected by the drug treatments in all tissues studied. In vitro the selective COX-2 inhibitor SC-236 caused a marked reduction in adrenocorticotropic hormone-driven corticosterone release, as did the nonselective COX inhibitor, indomethacin. These results support a role of COX-2 in the manifestation of the HPA responses to endotoxin, particularly within the adrenal gland.
Similar articles
-
Effect of constitutive- and inducible-cyclooxygenase in the carbachol-induced pituitary-adrenocortical response during social stress.J Physiol Pharmacol. 2002 Sep;53(3):453-62. J Physiol Pharmacol. 2002. PMID: 12369741
-
Effects of the inhibition of cyclo-oxygenase 1 or 2 or 5-lipoxygenase on the activation of the hypothalamic-pituitary-adrenal axis induced by interleukin-1beta in the male Rat.J Neuroendocrinol. 2000 Aug;12(8):766-73. doi: 10.1046/j.1365-2826.2000.00517.x. J Neuroendocrinol. 2000. PMID: 10929089
-
Influence of cyclooxygenase inhibitors on the central histaminergic stimulations of hypothalamic - pituitary - adrenal axis.J Physiol Pharmacol. 2003 Dec;54(4):643-52. J Physiol Pharmacol. 2003. PMID: 14726617
-
Nitric oxide and prostaglandin systems in the stimulation of hypothalamic-pituitary-adrenal axis by neurotransmitters and neurohormones.J Physiol Pharmacol. 2004 Dec;55(4):679-703. J Physiol Pharmacol. 2004. PMID: 15613736 Review.
-
Molecular mechanisms involved in the regulation of prostaglandin biosynthesis by glucocorticoids.Biochem Pharmacol. 1997 May 15;53(10):1389-95. doi: 10.1016/s0006-2952(97)00018-x. Biochem Pharmacol. 1997. PMID: 9260864 Review.
Cited by
-
Celecoxib reduces glucocorticoids in vitro and in a mouse model with adrenocortical hyperplasia.Endocr Relat Cancer. 2016 Jan;23(1):15-25. doi: 10.1530/ERC-15-0472. Epub 2015 Oct 5. Endocr Relat Cancer. 2016. PMID: 26438728 Free PMC article.
-
Cerebrovascular cyclooxygenase-1 expression, regulation, and role in hypothalamic-pituitary-adrenal axis activation by inflammatory stimuli.J Neurosci. 2009 Oct 14;29(41):12970-81. doi: 10.1523/JNEUROSCI.2373-09.2009. J Neurosci. 2009. PMID: 19828811 Free PMC article.
-
Repeated predictable stress causes resilience against colitis-induced behavioral changes in mice.Front Behav Neurosci. 2014 Nov 6;8:386. doi: 10.3389/fnbeh.2014.00386. eCollection 2014. Front Behav Neurosci. 2014. PMID: 25414650 Free PMC article.
-
Anti-inflammatory effects of angiotensin receptor blockers in the brain and the periphery.Cell Mol Neurobiol. 2009 Sep;29(6-7):781-92. doi: 10.1007/s10571-009-9368-4. Epub 2009 Mar 4. Cell Mol Neurobiol. 2009. PMID: 19259805 Free PMC article. Review.
-
Angiotensin II AT1 receptor blockade decreases lipopolysaccharide-induced inflammation in the rat adrenal gland.Endocrinology. 2008 Oct;149(10):5177-88. doi: 10.1210/en.2008-0242. Epub 2008 Jun 12. Endocrinology. 2008. PMID: 18556352 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials