Literature DB >> 8179808

Renal effects of rapamycin in the spontaneously hypertensive rat.

J F DiJoseph1, M J Mihatsch, S N Sehgal.   

Abstract

The effects of rapamycin (RAPA), administered at therapeutic doses, were investigated in the spontaneously hypertensive rat (SHR). Additionally, the reversibility of RAPA's renal effects was investigated at a supratherapeutic dose. At doses that were active in preventing heart and kidney allograft rejection in the rat (0.01-0.08 mg/kg i.v.), RAPA had no effect on kidney function or rat body weight gain. At higher doses (0.8 mg/kg), RAPA produced significant changes in kidney function parameters and caused a loss in body weight. Histopathologic changes, including necrotizing vasculopathy and tubular atrophy, were noted at therapeutic doses. The effects of RAPA on kidney function were completely reversible after a 2-week washout period, though the histopathologic changes were still evident. These studies demonstrate that RAPA does not impair kidney function at therapeutic doses when administered for 2 weeks but does appear to accelerate the naturally occurring renal lesions of the SHR.

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Year:  1994        PMID: 8179808     DOI: 10.1007/bf00336467

Source DB:  PubMed          Journal:  Transpl Int        ISSN: 0934-0874            Impact factor:   3.782


  6 in total

1.  Mammalian target of rapamycin is a critical regulator of cardiac hypertrophy in spontaneously hypertensive rats.

Authors:  Will Soesanto; Han-Yi Lin; Eric Hu; Shane Lefler; Sheldon E Litwin; Sandra Sena; E Dale Abel; J David Symons; Thunder Jalili
Journal:  Hypertension       Date:  2009-11-02       Impact factor: 10.190

2.  Clinical outcomes in kidney transplant recipients receiving long-term therapy with inhibitors of the mammalian target of rapamycin.

Authors:  F Cortazar; M Z Molnar; T Isakova; M E Czira; C P Kovesdy; D Roth; I Mucsi; M Wolf
Journal:  Am J Transplant       Date:  2011-11-04       Impact factor: 8.086

Review 3.  Roles of mTOR complexes in the kidney: implications for renal disease and transplantation.

Authors:  Daniel Fantus; Natasha M Rogers; Florian Grahammer; Tobias B Huber; Angus W Thomson
Journal:  Nat Rev Nephrol       Date:  2016-08-01       Impact factor: 28.314

4.  Inhibition of Mammalian Target of Rapamycin Complex 1 Attenuates Salt-Induced Hypertension and Kidney Injury in Dahl Salt-Sensitive Rats.

Authors:  Vikash Kumar; Clayton Wollner; Theresa Kurth; John D Bukowy; Allen W Cowley
Journal:  Hypertension       Date:  2017-08-21       Impact factor: 10.190

5.  Everolimus treatment downregulates renocortical cyclooxygenase-2 expression in the rat kidney.

Authors:  Klaus Höcherl; Corina Hensel; Bettina Ulbricht; Bernhard K Krämer
Journal:  Br J Pharmacol       Date:  2005-08       Impact factor: 8.739

Review 6.  Benefit-risk assessment of sirolimus in renal transplantation.

Authors:  Dirk R J Kuypers
Journal:  Drug Saf       Date:  2005       Impact factor: 5.606

  6 in total

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