Glycine Supplementation in Obesity Worsens Glucose Intolerance through Enhanced Liver Gluconeogenesis.
Anaïs AlvesFrédéric LamarcheRémy LefebvreEva Drevet MulardArthur BassotStephanie ChanonEmmanuelle LoizonClaudie PinteurAline Maria Nunes de Lira Gomes BloiseMurielle GodetGilles Jeans Philippe RautureauBaptiste PanthuBéatrice MorioPublished in: Nutrients (2022)
Interactions between mitochondria and the endoplasmic reticulum, known as MAMs, are altered in the liver in obesity, which contributes to disruption of the insulin signaling pathway. In addition, the plasma level of glycine is decreased in obesity, and the decrease is strongly correlated with the severity of insulin resistance. Certain nutrients have been shown to regulate MAMs; therefore, we tested whether glycine supplementation could reduce insulin resistance in the liver by promoting MAM integrity. Glycine (5 mM) supported MAM integrity and insulin response in primary rat hepatocytes cultured under control and lipotoxic (palmitate 500 µM) conditions for 18 h. In contrast, in C57 BL/6 JOlaHsd mice (male, 6 weeks old) fed a high-fat, high-sucrose diet (HFHS) for 16 weeks, glycine supplementation (300 mg/kg) in drinking water during the last 6 weeks (HFHS-Gly) did not reverse the deleterious impact of HFHS-feeding on liver MAM integrity. In addition, glycine supplementation worsened fasting glycemia and glycemic response to intraperitoneal pyruvate injection compared to HFHS. The adverse impact of glycine supplementation on hepatic gluconeogenesis was further supported by the higher oxaloacetate/acetyl-CoA ratio in the liver in HFHS-Gly compared to HFHS. Although glycine improves MAM integrity and insulin signaling in the hepatocyte in vitro, no beneficial effect was found on the overall metabolic profile of HFHS-Gly-fed mice.
Keyphrases
- insulin resistance
- type diabetes
- high fat diet induced
- metabolic syndrome
- drinking water
- weight loss
- endoplasmic reticulum
- glycemic control
- adipose tissue
- signaling pathway
- high fat diet
- blood glucose
- skeletal muscle
- magnetic resonance
- endothelial cells
- cell death
- oxidative stress
- body mass index
- fatty acid
- pi k akt
- adverse drug