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Lithium treatment inhibits renal GSK-3 activity and promotes cyclooxygenase 2-dependent polyuria.
Rao R, Zhang MZ, Zhao M, Cai H, Harris RC, Breyer MD, Hao CM
(2005) Am J Physiol Renal Physiol 288: F642-9
MeSH Terms: Adjuvants, Immunologic, Animals, Cells, Cultured, Cyclooxygenase 1, Cyclooxygenase 2, Diabetes Insipidus, Dinoprostone, Gene Expression Regulation, Enzymologic, Glycogen Synthase Kinase 3, Glycogen Synthase Kinase 3 beta, Kidney Medulla, Lithium Chloride, Male, Membrane Proteins, Mice, Mice, Inbred C57BL, Mice, Mutant Strains, Microsomes, Osmolar Concentration, Polyuria, Prostaglandin-Endoperoxide Synthases, Rats, Rats, Brattleboro
Show Abstract · Added January 28, 2014
The use of LiCl in clinical psychiatry is routinely complicated by overt nephrogenic diabetes insipidus (NDI), the mechanism of which is incompletely understood. In vitro studies indicate that lithium can induce renal medullary interstitial cell cyclooxygenase 2 (COX2) protein expression via inhibition of glycogen synthase kinase-3beta (GSK-3beta). Both COX1 and COX2 are expressed in the kidney. Renal prostaglandins have been suggested to play an important role in lithium-induced polyuria. The present studies examined whether induction of the COX2 isoform contributes to LiCl-induced polyuria. Four days after initiation of lithium treatment in C57 BL/6J mice, urine volume increased in LiCl-treated mice by fourfold compared with controls (P < 0.0001) and was accompanied by decreased urine osmolality. This was temporally associated with increased renal COX2 protein expression and increased urinary PGE(2) excretion, whereas COX1 levels remained unchanged. COX2 inhibition significantly blunted lithium-induced polyuria (P < 0.0001) and reduced urinary PGE(2) levels. Lithium-associated polyuria was also seen in COX1-/- mice and was associated with increased urinary PGE(2). COX2 inhibition completely prevented polyuria and PGE(2) excretion in COX1-/- mice, suggesting that COX2, but not COX1, plays a critical role in lithium-induced polyuria. Lithium also induced renal medullary COX2 protein expression in congenitally polyuric antidiuretic hormone (AHD)-deficient rats, demonstrating that lithium-induced COX2 protein expression is not secondary to altered ADH levels or polyuria. Lithium also decreased renal medullary GSK-3beta activity, and this was temporally related to increased COX2 expression in the kidney from lithium-treated mice, consistent with a tonic in vivo suppression of COX2 expression by GSK-3 activity. In conclusion, these findings temporally link decreased GSK-3 activity to enhanced renal COX2 expression and COX2-derived urine PGE(2) excretion. Suppression of COX2-derived PGE(2) blunts lithium-associated polyuria.
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23 MeSH Terms
Regulation of cyclooxygenase expression by vasopressin in rat renal medulla.
Zhang MZ, Sanchez Lopez P, McKanna JA, Harris RC
(2004) Endocrinology 145: 1402-9
MeSH Terms: Animals, Cyclooxygenase 1, Cyclooxygenase 2, Dinoprostone, Down-Regulation, Immunohistochemistry, In Vitro Techniques, Isoenzymes, Kidney Medulla, Male, Membrane Proteins, Osmolar Concentration, Prostaglandin-Endoperoxide Synthases, Rats, Rats, Brattleboro, Rats, Long-Evans, Receptors, Vasopressin, Up-Regulation, Vasopressins
Show Abstract · Added December 10, 2013
The antagonism between prostaglandin and vasopressin represents a classic negative feedback loop. It is not clear whether cyclooxygenase (COX)-2 and/or COX-1 expression is involved in elevated prostaglandin production stimulated by vasopressin in vivo. In the present study, we explored vasopressin regulation of medullary COX-2 and COX-1 expression acutely and chronically in rats. Medullary COX-1 expression was moderately lower and COX-2 expression was significantly lower in adult male Brattleboro rats than age-matched Long-Evans controls. Chronic treatment of Brattleboro rats with vasopressin for 1 wk led to a decrease in urine volume and a moderate increase in medullary COX-1; in contrast, medullary COX-2 expression was almost undetectable in untreated rats but was dramatically up-regulated with vasopressin treatment and was accompanied by increased urinary prostaglandin E(2) excretion. Further investigation revealed that both V1 and V2 receptors were involved in chronic medullary COX-1 and COX-2 up-regulation. Acute treatment with specific V1 or V2 receptor agonists resulted in specific increases in medullary COX-2, which was prevented by furosemide. Vasopressin did not affect COX-2 expression in cultured renomedullary interstitial cells. These data demonstrate that vasopressin stimulates medullary COX-2 expression through activation of both V1 and V2 receptors, and this stimulation is indirect and probably involves increased medullary electrolyte tonicity.
1 Communities
2 Members
1 Resources
19 MeSH Terms
Mineralocorticoid regulation of cyclooxygenase-2 expression in rat renal medulla.
Zhang MZ, Hao CM, Breyer MD, Harris RC, McKanna JA
(2002) Am J Physiol Renal Physiol 283: F509-16
MeSH Terms: Adrenalectomy, Animals, Blotting, Western, Cells, Cultured, Cyclooxygenase 2, Desoxycorticosterone, Diabetes Insipidus, Epithelial Cells, Female, Homeostasis, Isoenzymes, Kidney Medulla, Male, Mineralocorticoid Receptor Antagonists, Mineralocorticoids, Prostaglandin-Endoperoxide Synthases, Rats, Rats, Brattleboro, Rats, Sprague-Dawley, Receptors, Glucocorticoid, Receptors, Mineralocorticoid, Spironolactone
Show Abstract · Added December 10, 2013
The renal inner medulla and its distal one-third, the papilla, are major sites of prostanoid synthesis involved in water and electrolyte homeostasis. These sites contain variable levels of cyclooxygenase (COX)-2, a key prostaglandin synthase enzyme that is sensitive to adrenal steroids. Immunoreactive renal medullary COX-2, restricted to interstitial cells in control adult rats, shows a gradient of intense staining at the tip of the papilla that gradually diminishes to undetectable levels in the proximal inner medulla. We used adrenalectomy (ADX) and steroid replacement to investigate the effects of steroids on papillary COX-2. Immunoblots demonstrate that papillary COX-2 was reduced by one-half after 2 wk ADX; glucocorticoid replacement ameliorated the decline but not to control levels. Mineralocorticoid (deoxycorticosterone acetate; DOCA) replacement stimulated papillary COX-2 more than fivefold over control; both the intensity of immunostaining and the numbers of COX-2-positive cells in the inner medulla increased. Similar stimulation of papillary COX-2 resulted from DOCA treatment of normal control rats, but the response was blunted in rats fed a low-salt diet and absent in Brattleboro rats. DOCA treatment of mouse renal medullary interstitial cells in culture had no effect, but increased tonicity of the culture medium with NaCl caused strong upregulation of COX-2. Urea, a permeant molecule, had no effect. Together, these results suggest that mineralocorticoids lead to upregulation of COX-2 in rat renal medulla by indirect pathways, probably involving induced electrolyte hypertonicity in the interstitial fluid.
1 Communities
2 Members
0 Resources
22 MeSH Terms
Vasopressin modulates liver regeneration in the Brattleboro rat.
Russell WE, Bucher NL
(1983) Am J Physiol 245: G321-4
MeSH Terms: Animals, Arginine Vasopressin, DNA Replication, Kinetics, Liver, Liver Regeneration, Male, Rats, Rats, Brattleboro, Rats, Mutant Strains, Species Specificity
Show Abstract · Added December 10, 2013
Liver regeneration following partial hepatectomy is significantly impaired in rats with hereditary vasopressin deficiency (Brattleboro strain), both in rate of DNA synthesis and in return of liver DNA content to normal. Vasopressin treatment at physiological doses ameliorates the defect and thus appears to be an important modulator of liver regeneration in response to partial hepatectomy in the rat.
0 Communities
1 Members
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11 MeSH Terms