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Modulation by exercise of glucose and protein metabolism in alloxan diabetic rats

Grant number: 05/02254-3
Support Opportunities:Scholarships in Brazil - Technical Training Program - Technical Training
Start date: January 01, 2006
End date: December 31, 2006
Field of knowledge:Biological Sciences - Physiology - Physiology of Effort
Principal Investigator:Maria Alice Rostom de Mello
Grantee:Kátia Carnier
Host Institution: Instituto de Biociências (IB). Universidade Estadual Paulista (UNESP). Campus de Rio Claro. Rio Claro , SP, Brazil
Associated research grant:05/02139-0 - Modulation by exercise of glucose and protein metabolism in alloxan diabetic rats, AP.R

Abstract

Exercise has been recommended in the treatment of diabetes mellitus and its metabolic complications, but the mechanisms involved in this intervention are not fully understood. Researches using animal models offer great opportunity to a deeper comprehension about this issue. However, some results have been questioned due the lack of information about the effort intensity performed by the animal during exercise. This way, the present study was designed to analyse the effects of physical training performed at the anaerobic threshold (AT) intensity, on glucose and protein metabolism in skeletal muscle of alloxan diabetic rats. Wistar young rats will receive alloxan monohidrate Sigma (30 mg/Kg of body weight, i.v.). Rats injected with citrate buffer will be used as controls. Two weeks after drug administration, the animals will perform the lactate minimum test in order to identify the AT and, from this moment on, they will be submitted to swimming training 1h/day, 5 days/week, carriyng an overload equivalent to Lan, during 6 weeks. The "in vivo" evaluations include glucose tolerance and insulin sensibility. Forty eight hours after the last training session, the rats will be sacrificed for biological material collection to "in vitro" analysis in the soleus muscle: glucose uptake and oxidation, glycogen synthesis, lactate production, protein synthesis and degradation and celular sinalization of the ubiquitin-proteasome proteolytic pathway.

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