Adipocyte-derived factor reduces vasodilatory capability in ob−/ob− mice

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American Physiological Society

RESUMO

Obesity is associated with impaired functional hyperemic response. We have shown that ATP-sensitive potassium (KATP) channels are important in mediating functional vasodilation. Adipocyte-derived factors (ADFs) can alter vascular tone via opening KATP channels. We hypothesize that, in an animal model of obesity, ADFs will decrease basal arteriolar tone by opening KATP channels, resulting in an attenuated functional vasodilation. We used wild-type (WT) mice and ob−/ob− mice (ob) to test this hypothesis. The spinotrapezius muscle was prepared for the microcirculatory observation of arcade arterioles, and we measured the vasodilatory responses to muscle stimulation. The basal arteriolar diameter was larger in ob mice compared with WT mice. The KATP channel inhibitor glibenclamide (10 μM) decreased arteriolar diameter in ob mice with no effect in WT mice. The increase in arteriolar diameter induced by muscle stimulation was attenuated in ob mice compared with WT mice. To determine the mechanisms for the opening of KATP channels, fat was collected from the ob mice, subcutaneous fat from around the spinotrapezius muscle (OBSF) or visceral fat (OBVF) and was incubated in physiological saline solution (PSS). The vasodilatory responses to the fat-conditioned PSS were determined in WT mice. Treatment with OBSF- or OBVF -conditioned PSS increased the arteriolar diameters in WT mice, a dilation that was inhibited by glibenclamide. The absolute diameters induced by muscle stimulation were not altered by the fat-conditioned PSS. These results suggest that, in ob mice, local ADFs reduce the functional vasodilatory capability via opening KATP channels.

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