PP.12.13

Abstract

Objective: High fat diet (HFD) induced hypertension in rabbits is neurogenic and due to the central action of leptin. This action is dependent on secondary neuronal activation in alpha-melanocortin stimulating hormone (alpha-MSH) and neuropeptide Y (NPY) positive cells. Neurons in the ventromedial hypothalamus (VMH) and Dorsomedial hypothalamus (DMH) are innervated by both neuronal populations and transduce leptin signaling from the Arcuate to other hypothalamic and hindbrain nuclei. The VMH and DMH are also capable of responding to leptin signals directly, independent of NPY or alpha-MSH neurons. In the present study we assessed the contribution of leptin, alpha-MSH and NPY neurons in the VMH and DMH on development of diet-induced neurogenic hypertension. Design and method: Male New Zealand White rabbits were instrumented with a VMH or DMH cannula and a renal sympathetic nerve electrode. Blood pressure was measured by means of an intra-arterial catheter. Following 3 weeks of a HFD (13.5 % fat, n = 10) conscious rabbits had higher renal sympathetic nerve activity (RSNA), blood pressure and heart rate compared with control diet-fed animals (3.5 % fat, n = 10). Results: Rabbits exhibited higher blood pressure, heart rate and renal sympathetic nerve activity when fed a high fat diet compared to controls (n = 6–10). Alpha-melanocyte-stimulating hormone injection into the ventromedial hypothalamus increased blood pressure and renal sympathetic nerve activity (P < 0.05) in high fat diet rabbits. By contrast, no changes were observed in blood pressure or renal sympathetic nerve activity following alpha-melanocyte-stimulating hormone injections into the dorsomedial hypothalamus. Leptin antagonist injection into ventromedial and dorsomedial hypothalamus decreased blood pressure (P < 0.05) when given to high fat diet rabbits. Neuropeptide Y injection had no effect on blood pressure or renal sympathetic nerve activity in either nuclei. Conclusions: We conclude that the VMH is the likely origin of leptin-mediated sympathoexcitation, alpha-MSH hypersensitivity and altered central responsiveness to NPY.