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1.
Lipids Health Dis ; 16(1): 245, 2017 Dec 16.
Article in English | MEDLINE | ID: mdl-29246161

ABSTRACT

BACKGROUND: Undernutrition during childhood leads to chronic diseases in adult life including hypertension, diabetes and chronic kidney disease. Here we explore the hypothesis that physiological alterations in the bioactive lipids pattern within kidney tissue might be involved in the progression of chronic kidney disease. METHODS: Membrane fractions from kidney homogenates of undernourished rats (RBD) were submitted to lipid extraction and analysis by thin layer chromatography and cholesterol determination. RESULTS: Kidneys from RBD rats had 25% lower cholesterol content, which disturb membrane microdomains, affecting Ca2+ homeostasis and the enzymes responsible for important lipid mediators such as phosphatidylinositol-4 kinase, sphingosine kinase, diacylglicerol kinase and phospholipase A2. We observed a decrease in phosphatidylinositol(4)-phosphate (8.8 ± 0.9 vs. 3.6 ± 0.7 pmol.mg-1.mim-1), and an increase in phosphatidic acid (2.2 ± 0.8 vs. 3.8 ± 1.3 pmol.mg-1.mim-1), being these lipid mediators involved in the regulation of key renal functions. Ceramide levels are augmented in kidney tissue from RBD rats (18.7 ± 1.4 vs. 21.7 ± 1.5 fmol.mg-1.min-1) indicating an ongoing renal lesion. CONCLUSION: Results point to an imbalance in the bioactive lipid generation with further consequences to key events related to kidney function, thus contributing to the establishment of chronic kidney disease.


Subject(s)
Cholesterol/metabolism , Hypertension/metabolism , Kidney/metabolism , Malnutrition/metabolism , Phosphatidylinositol Phosphates/metabolism , Renal Insufficiency, Chronic/metabolism , 1-Phosphatidylinositol 4-Kinase/genetics , 1-Phosphatidylinositol 4-Kinase/metabolism , Animals , Animals, Newborn , Ceramides/metabolism , Diacylglycerol Kinase/genetics , Diacylglycerol Kinase/metabolism , Gene Expression Regulation , Hypertension/etiology , Hypertension/genetics , Hypertension/pathology , Kidney/chemistry , Lipid Metabolism , Male , Malnutrition/complications , Malnutrition/genetics , Malnutrition/pathology , Membrane Microdomains/chemistry , Membrane Microdomains/metabolism , Phosphatidic Acids/metabolism , Phospholipases A2/genetics , Phospholipases A2/metabolism , Phosphotransferases (Alcohol Group Acceptor)/genetics , Phosphotransferases (Alcohol Group Acceptor)/metabolism , Rats , Rats, Wistar , Renal Insufficiency, Chronic/etiology , Renal Insufficiency, Chronic/genetics , Renal Insufficiency, Chronic/pathology
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