Literature DB >> 16649344

Sirolimus: mammalian target of rapamycin inhibitor to prevent kidney rejection.

P A Cowan1, K E Heizer.   

Abstract

Current immunosuppressive therapies are effective but can be associated with significant adverse reactions. Sirolimus works differently from the immunosuppressants currently available, and except for increased lipid levels, the adverse reaction profile of sirolimus does not appear to overlap to any great extent with that associated with cyclosporine or tacrolimus. While additional research is needed, the initial clinical data in kidney recipients suggest that sirolimus, in combination with cyclosporine or tacrolimus, might have the potential to reduce the frequency of rejection episodes, permit reductions in cyclosporine or tacrolimus dosage, and permit steroid withdrawal (Kelly, 1999).

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Year:  2000        PMID: 16649344

Source DB:  PubMed          Journal:  Nephrol Nurs J        ISSN: 1526-744X            Impact factor:   0.959


  3 in total

1.  Mammalian target of rapamycin inhibition abrogates insulin-mediated mammary tumor progression in type 2 diabetes.

Authors:  Yvonne Fierz; Ruslan Novosyadlyy; Archana Vijayakumar; Shoshana Yakar; Derek LeRoith
Journal:  Endocr Relat Cancer       Date:  2010-10-05       Impact factor: 5.678

2.  Short term treatment with a cocktail of rapamycin, acarbose and phenylbutyrate delays aging phenotypes in mice.

Authors:  Zhou Jiang; Juan Wang; Denise Imai; Tim Snider; Jenna Klug; Ruby Mangalindan; John Morton; Lida Zhu; Adam B Salmon; Jackson Wezeman; Jiayi Hu; Vinal Menon; Nicholas Marka; Laura Neidernhofer; Warren Ladiges
Journal:  Sci Rep       Date:  2022-05-04       Impact factor: 4.996

3.  Brain-specific inhibition of mTORC1 eliminates side effects resulting from mTORC1 blockade in the periphery and reduces alcohol intake in mice.

Authors:  Yann Ehinger; Ziyang Zhang; Khanhky Phamluong; Drishti Soneja; Kevan M Shokat; Dorit Ron
Journal:  Nat Commun       Date:  2021-07-27       Impact factor: 14.919

  3 in total

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