Literature DB >> 15569301

Retinoids in nephrology: promises and pitfalls.

Qihe Xu1, Javier Lucio-Cazana, Masanori Kitamura, Xiongzhong Ruan, Leon G Fine, Jill T Norman.   

Abstract

BACKGROUND: Retinoids, a family of vitamin A metabolites or analogs, play an important role in regulating cell proliferation, differentiation, and apoptosis.
METHODS: The biological importance of retinoids in the kidney and the potential of retinoids in the treatment of renal diseases are reviewed.
RESULTS: Vitamin A deficiency and mutations of retinoid nuclear receptors cause abnormalities in fetal kidneys, which might predispose to adult diseases such as hypertension. Further, the therapeutic value of retinoids in animal models of kidney diseases, such as lupus nephritis, puromycin aminonucleoside nephrosis, anti-glomerular basement membrane nephritis, mesangioproliferative nephritis, and acute renal allograft rejection has been unveiled recently. Retinoids target mesangial cells, podocytes, tubular epithelial cells, interstitial fibroblasts, as well as lymphocytes and macrophages. The anti-inflammation, anti-coagulation effects, and the proliferation- and immunity-modulating actions of retinoids, have been widely appreciated. Our recent in vitro data revealed a direct antifibrotic effect and a cytoprotective effect of retinoids in various renal cell types. In animal studies, the adverse effects of retinoids are generally minimal; however, the clinical use of retinoids in other diseases points to some major side effects. In addition, in vitro, retinoids can induce lipid accumulation in smooth muscle cells and macrophages and increase expression of some proinflammatory molecules, indicating that their clinical toxicity profile in the setting of renal diseases needs to be better understood.
CONCLUSION: Retinoids not only are important in renal development, but also show promise as a new generation of renal medication and deserve to be tested in clinical trials to clarify their full potential.

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Year:  2004        PMID: 15569301     DOI: 10.1111/j.1523-1755.2004.66002.x

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  29 in total

1.  Increased unbound retinol-binding protein 4 concentration induces apoptosis through receptor-mediated signaling.

Authors:  Chao-Hung Chen; Tusty-Jiuan Hsieh; Kun-Der Lin; Hsing-Yi Lin; Mei-Yueh Lee; Wei-Wen Hung; Pi-Jung Hsiao; Shyi-Jang Shin
Journal:  J Biol Chem       Date:  2012-02-03       Impact factor: 5.157

2.  An in vitro model for the pro-fibrotic effects of retinoids: mechanisms of action.

Authors:  A C Rankin; B M Hendry; J P Corcoran; Q Xu
Journal:  Br J Pharmacol       Date:  2013-11       Impact factor: 8.739

Review 3.  Retinoic acid signaling pathways in development and diseases.

Authors:  Bhaskar C Das; Pritam Thapa; Radha Karki; Sasmita Das; Sweta Mahapatra; Ting-Chun Liu; Ingrid Torregroza; Darren P Wallace; Suman Kambhampati; Peter Van Veldhuizen; Amit Verma; Swapan K Ray; Todd Evans
Journal:  Bioorg Med Chem       Date:  2013-11-22       Impact factor: 3.641

4.  Kinase-dependent, retinoic acid receptor-independent up-regulation of cyclooxygenase-2 by all-trans retinoic acid in human mesangial cells.

Authors:  M Alique; V Moreno; M Kitamura; Q Xu; F J Lucio-Cazana
Journal:  Br J Pharmacol       Date:  2006-08-07       Impact factor: 8.739

Review 5.  The membrane receptor for plasma retinol-binding protein, a new type of cell-surface receptor.

Authors:  Hui Sun; Riki Kawaguchi
Journal:  Int Rev Cell Mol Biol       Date:  2011       Impact factor: 6.813

6.  Retinoic acid improves nephrotoxic serum-induced glomerulonephritis through activation of podocyte retinoic acid receptor α.

Authors:  Yan Dai; Anqun Chen; Ruijie Liu; Leyi Gu; Shuchita Sharma; Weijing Cai; Fadi Salem; David J Salant; Jeffrey W Pippin; Stuart J Shankland; Marcus J Moeller; Norbert B Ghyselinck; Xiaoqiang Ding; Peter Y Chuang; Kyung Lee; John Cijiang He
Journal:  Kidney Int       Date:  2017-07-27       Impact factor: 10.612

7.  Kidneys of Alb/TGF-beta1 transgenic mice are deficient in retinoic acid and exogenous retinoic acid shows dose-dependent toxicity.

Authors:  Qihe Xu; Bruce M Hendry; Malcolm Maden; Huiyan Lu; Yuen Fei Wong; Alexandra C Rankin; Mazhar Noor; Jeffrey B Kopp
Journal:  Nephron Exp Nephrol       Date:  2010-01-21

8.  Inhibition of HDAC enhances STAT acetylation, blocks NF-κB, and suppresses the renal inflammation and fibrosis in Npr1 haplotype male mice.

Authors:  Prerna Kumar; Venkateswara R Gogulamudi; Ramu Periasamy; Giri Raghavaraju; Umadevi Subramanian; Kailash N Pandey
Journal:  Am J Physiol Renal Physiol       Date:  2017-05-31

9.  All-trans retinoic acid potentiates cisplatin-induced kidney injury in rats: impact of retinoic acid signaling pathway.

Authors:  Abdelrahman M Elsayed; Tamer M Abdelghany; El-Sayed Akool; Abdel-Aziz H Abdel-Aziz; Mohamed S Abdel-Bakky
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2015-12-11       Impact factor: 3.000

10.  Effect of all-trans retinoic acid on renal expressions of matrix metalloproteinase-2, matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 in rats with glomerulosclerosis.

Authors:  Yuan-Han Qin; Feng-Ying Lei; Peng Hu; Juan Pei; Zhen-Bo Feng; Yu-Sheng Pang
Journal:  Pediatr Nephrol       Date:  2009-04-09       Impact factor: 3.714

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