z-logo
open-access-imgOpen Access
Rapamycin Increases Mortality indb/dbMice, a Mouse Model of Type 2 Diabetes
Author(s) -
Kavithalakshmi Sataranatarajan,
Yuji Ikeno,
Alex Bokov,
Denis Féliers,
Himabindu Yalamanchili,
Hak Joo Lee,
Meenalakshmi M. Mariappan,
Hooman Tabatabai-Mir,
Vivian Diaz,
Sanjay Prasad,
Martin A. Javors,
Goutam Ghosh Choudhury,
Gene B. Hubbard,
Jeffrey L. Barnes,
Arlan Richardson,
Balakuntalam S. Kasinath
Publication year - 2015
Publication title -
the journals of gerontology series a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.134
H-Index - 189
eISSN - 1758-535X
pISSN - 1079-5006
DOI - 10.1093/gerona/glv170
Subject(s) - life span , diabetes mellitus , endocrinology , type 2 diabetes , medicine , pathological , inflammation , biology , gerontology
We examined the effect of rapamycin on the life span of a mouse model of type 2 diabetes, db/db mice. At 4 months of age, male and female C57BLKSJ-lepr (db/db) mice (db/db) were placed on either a control diet, lacking rapamycin or a diet containing rapamycin and maintained on these diets over their life span. Rapamycin was found to reduce the life span of the db/db mice. The median survival of male db/db mice fed the control and rapamycin diets was 349 and 302 days, respectively, and the median survival of female db/db mice fed the control and rapamycin diets was 487 and 411 days, respectively. Adjusting for gender differences, rapamycin increased the mortality risk 1.7-fold in both male and female db/db mice. End-of-life pathological data showed that suppurative inflammation was the main cause of death in the db/db mice, which is enhanced slightly by rapamycin treatment.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom