Intra-Abdominal Fat Adipocyte Hypertrophy through a Progressive Alteration of Lipolysis and Lipogenesis in Metabolic Syndrome Rats.
Israel Pérez-TorresYolanda Gutiérrez-AlvarezVerónica Guarner-LansEulises Díaz-DíazLinaloe Manzano PechSara Del Carmen Caballero-ChacónPublished in: Nutrients (2019)
This study evaluates the progressive participation of enzymes involved in lipolysis and lipogenesis, leading to adipocyte hypertrophy in a metabolic syndrome (MS) rat model caused by chronic consumption of 30% sucrose in drinking water. A total of 70 male Wistar rats were divided into two groups: C and MS. Each of these groups were then subdivided into five groups which were sacrificed as paired groups every month from the beginning of the treatment until 5 months. The intra-abdominal fat was dissected, and the adipocytes were extracted. Lipoprotein lipase (LPL), hormone-sensitive lipase (HSL), protein kinases A (PKA), and perilipin A expressions were determined. The LPL and HSL activities were evaluated by spectrophotometry. Histological staining was performed in adipose tissue. Significant increases were observed in blood pressure, HOMA-IR, leptin, triglycerides, insulin, intra-abdominal fat, and number of fat cells per field (p = 0.001) and in advanced glycosylation products, adipocyte area, LPL, HSL activities and/or expression (p ≤ 0.01) in the MS groups progressively from the third month onward. Lipogenesis and lipolysis were increased by LPL activity and HSL activity and/or expression. This was associated with hyperinsulinemia and release of non-esterified fatty acids causing a positive feedback loop that contributes to the development of adipocyte hypertrophy.
Keyphrases
- adipose tissue
- insulin resistance
- multiple sclerosis
- metabolic syndrome
- drinking water
- high fat diet induced
- high fat diet
- mass spectrometry
- fatty acid
- blood pressure
- poor prognosis
- ms ms
- type diabetes
- binding protein
- uric acid
- physical activity
- risk assessment
- small molecule
- cardiovascular disease
- protein protein
- cell cycle arrest
- signaling pathway
- flow cytometry
- drug induced
- hypertensive patients