Literature DB >> 18093581

Actinonin, a meprin inhibitor, protects ischemic acute kidney injury in male but not in female rats.

Junji Takayama1, Masanori Takaoka, Shinya Yamamoto, Asami Nohara, Mamoru Ohkita, Yasuo Matsumura.   

Abstract

We investigated the effects of actinonin, an inhibitor of a matrix-degrading enzyme meprin, on ischemic acute kidney injury in male and female rats, and these were compared with the effects of verapamil, a Ca(2+) channel blocker. Ischemic acute kidney injury was induced by occlusion of the left renal artery and vein for 45 min followed by reperfusion, 2 weeks after contralateral nephrectomy. At 24 h after reperfusion, renal function and histology of both males and females showed significant deterioration. The degrees of renal dysfunction and histological damage were much more severe in males than in females. Pre-ischemic treatment with actinonin (10 or 30 mg/kg, i.v.) dose-dependently attenuated the ischemia/reperfusion-induced renal injury in male rats, but failed to improve the renal injury in female rats. On the other hand, verapamil (1 mg/kg, i.v.) could efficiently prevent the ischemic acute kidney injury in female rats, as well as male rats. These results indicate that the renoprotective effect of actinonin is male-specific, thereby suggesting that meprin is involved in exacerbation of ischemia/reperfusion-induced renal injury in male rats. The possibility that meprin is a key factor involved in the sex difference in the pathogenesis of ischemic acute kidney injury, warrants further attention.

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Year:  2007        PMID: 18093581     DOI: 10.1016/j.ejphar.2007.11.044

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  9 in total

Review 1.  Meprin A metalloproteinase and its role in acute kidney injury.

Authors:  Gur P Kaushal; Randy S Haun; Christian Herzog; Sudhir V Shah
Journal:  Am J Physiol Renal Physiol       Date:  2013-02-20

2.  Actinonin, a meprin A inhibitor, protects the renal microcirculation during sepsis.

Authors:  Zhen Wang; Christian Herzog; Gur P Kaushal; Neriman Gokden; Philip R Mayeux
Journal:  Shock       Date:  2011-02       Impact factor: 3.454

3.  B-type natriuretic peptide 8-32, which is produced from mature BNP 1-32 by the metalloprotease meprin A, has reduced bioactivity.

Authors:  Guido Boerrigter; Lisa C Costello-Boerrigter; Gail J Harty; Brenda K Huntley; Alessandro Cataliotti; Harald Lapp; John C Burnett
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2009-04-22       Impact factor: 3.619

4.  ADAM10 is the major sheddase responsible for the release of membrane-associated meprin A.

Authors:  Christian Herzog; Randy S Haun; Andreas Ludwig; Sudhir V Shah; Gur P Kaushal
Journal:  J Biol Chem       Date:  2014-03-24       Impact factor: 5.157

Review 5.  The metalloproteases meprin α and meprin β: unique enzymes in inflammation, neurodegeneration, cancer and fibrosis.

Authors:  Claudia Broder; Christoph Becker-Pauly
Journal:  Biochem J       Date:  2013-03-01       Impact factor: 3.857

6.  Hypoxia Associated Proteolytic Processing of OS-9 by the Metalloproteinase Meprin β.

Authors:  Barry Lee Martin; Sabena Michelle Conley; Regine Simone Harris; Corshe Devon Stanley; Jean-Marie Vianney Niyitegeka; Elimelda Moige Ongeri
Journal:  Int J Nephrol       Date:  2016-07-13

7.  Gender Differences in the Acute Kidney Injury to Chronic Kidney Disease Transition.

Authors:  Ixchel Lima-Posada; Cinthya Portas-Cortés; Rosalba Pérez-Villalva; Francesco Fontana; Roxana Rodríguez-Romo; Rodrigo Prieto; Andrea Sánchez-Navarro; Guadalupe L Rodríguez-González; Gerardo Gamba; Elena Zambrano; Norma A Bobadilla
Journal:  Sci Rep       Date:  2017-09-25       Impact factor: 4.379

8.  Meprin β metalloproteases associated with differential metabolite profiles in the plasma and urine of mice with type 1 diabetes and diabetic nephropathy.

Authors:  Jessica Gooding; Lei Cao; Courtney Whitaker; Jean-Marie Mwiza; Mizpha Fernander; Faihaa Ahmed; Zach Acuff; Susan McRitchie; Susan Sumner; Elimelda Moige Ongeri
Journal:  BMC Nephrol       Date:  2019-04-25       Impact factor: 2.388

9.  Proteolysis controls endogenous substance P levels.

Authors:  Andrew J Mitchell; Anna Mari Lone; Arthur D Tinoco; Alan Saghatelian
Journal:  PLoS One       Date:  2013-07-19       Impact factor: 3.240

  9 in total

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