Title
Evidences of Basal lactate production in the main white adipose tissue sites of rats. effects of sex and a cafeteria diet
Date Issued
05 March 2015
Access level
open access
Resource Type
journal article
Author(s)
Agnelli S.
Sabater D.
Remesar X.
Fernández-López J.A.
Alemany M.
University of Barcelona
Publisher(s)
Public Library of Science
Abstract
Female and male adult Wistar rats were fed standard chow or a simplified cafeteria diet for one month. Then, the rats were killed and the white adipose tissue (WAT) in four sites: perigonadal, retroperitoneal, mesenteric and subcutaneous (inguinal) were sampled and frozen. The complete WAT weight in each site was measured. Gene expression analysis of key lipid and glucose metabolism enzymes were analyzed, as well as tissue and plasma lactate and the activity of lactate dehydrogenase. Lactate gradients between WAT and plasma were estimated. The influence of sex and diet (and indirectly WAT mass) on lactate levels and their relationships with lactate dehydrogenase activity and gene expressions were also measured. A main conclusion is the high production of lactate by WAT, practically irrespective of site, diet or sex. Lactate production is a direct correlate of lactate dehydrogenase activity in the tissue. Furthermore, lactate dehydrogenase activity is again directly correlated with the expression of the genes Ldha and Ldhb for this enzyme. In sum, the ability to produce lactate by WAT is not directly dependent of WAT metabolic state.We postulate that, in WAT, a main function of the lactate dehydrogenase path may be that of converting excess available glucose to 3C fragments, as a way to limit tissue self-utilization as substrate, to help control glycaemia and/or providing short chain substrates for use as energy source elsewhere. More information must be gathered before a conclusive role of WAT in the control of glycaemia, and the full existence of a renewed glucose-lactate-fatty acid cycle is definitely established.
Volume
10
Issue
3
Number
e0119572
Language
English
OCDE Knowledge area
Bioquímica, Biología molecular
Fisiología
Scopus EID
2-s2.0-84924309958
PubMed ID
Source
PLoS ONE
ISSN of the container
19326203
Sources of information:
Directorio de Producción Científica
Scopus