Metformin prevents vascular prostanoid release alteration induced by a high-fat diet in rats

LEE HJ; CANTÚ SM; DONOSO AS; CHOI MR; PEREDO H; PUYÓ AM

Autonomic and autacoid pharmacology

Blackwell Pub

Lugar: Oxford; Año: 2017

1474-8665

1. 1. Perivascular adipose tissue dysfunction induced by high fat feeding leads to alterations in the modulation of inflammation, contractile activity of the vascular smooth muscle and endothelial function, all risk factors in the development of hypertension. Metformin, an activator of AMP-activated protein kinase (AMPK), is currently the first-line drug treatment for type 2 diabetes (T2DM) and metabolic syndrome. Besides its glucose-lowering effect, there is an interest in actions of this drug with potential relevance in cardiovascular diseases.2. The high-fat (HF) diet is an experimental model that resembles human metabolic syndrome. We have previously reported an altered pattern of prostanoid release in mesenteric vessels in this model. 3. The aim of this study was to analyze the effects of metformin on mesenteric vascular bed prostanoid release, adiposity index and its relation to blood pressure in Sprague-Dawley rats fed a HF diet for 8 and 12 weeks. Eight groups were used: control (C8, C1), HF diet (HF8, HF12, 50% w/w bovine fat), metformin treated (CMf8, CMf12, 500 mg/Kg/day) and metformin-treated HF diet (HFMf8, HFMf12, both treatments). 4. HF diet increased mesenteric vascular bed adiposity index (%, HF8: 1.7±0.1 vs. C8: 0.9±0.04 and HF12: 1.8±0.1 vs. C12: 0.8±0.1, p<0.001); systolic blood pressure (SBP, mmHg, HF8: 145±6 vs. C8: 118±4, p<0.01 and HF12: 151±1 vs. C12: 121±3, p<0,001). We found a positive correlation between these two parameters. Moreover HF diet increased the release of vasoconstrictor prostanoids such as thromboxane (TX) B2 (ng PR/mg of tissue, HF8: 117±6 vs. C8: 66±2 and HF12: 123±6 vs. C12: 62±5, p<0,001) and prostaglandin (PG) F2α (ng/mg, HF8: 153±9 vs. C8: 88±3 and HF12: 160±11 vs. C12: 83±5, p<0,001). We also found that this increase in the release of vasoconstrictor prostanoids positively correlates with the elevation of SBP. In addition, HF diet increase therelease of PGE and decrease the prostacyclin (PGI2)/TXA2 release ratio at 8 and 12 weeks of treatment compared to control groups.5. In the HFMf group, metformin treatment prevented all these increases in mesenteric vascular bed adiposity index (%, HFMf8: 1.3±0.2 vs. HF8 and HFMf12: 1.3±0.1 vs. HF12, p<0.05); SBP (mmHg, HFMf8: 127±2 vs. HF8 and HFMf12: 132±1 vs. HF12, p<0.001); TXB2 release (ng PR/mg of tissue, HFMf8: 65±12 vs. HF8, p<0.05 and HFMf12: 53±3 vs. HF12, p<0.001) and PGF2α (ng PR/mg of tissue, HFMf8: 99±13 vs. HF8, p<0.01 and HFMf12: 77±8 vs. HF12, p<0.001). Meanwhile metformin prevented the increment in PGE2 release only at 12 weeks. On the other hand metformin improved the PGI2/TXA2 ratio in both periods studied.6. In conclusion, metformin could exert beneficial effects on adipose tissue and the vascular system by improving endothelial dysfunction induced by an imbalance of vasoactive substances in mesenteric perivascular adipose tissue in this model.