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OBESITY AND DIABETES: PATHOPHYSIOLOGICAL MECHANISMS AND THERAPEUTIC APPROACHES

Effects of Leptin on Hypothalamic Arcuate Neurons in Wistar and Zucker Rats: An In Vitro Study

Katsuhiko Nagamori^*, Masaru Ishibashi^*, Takemasa Shiraishi, Yutaka Oomura and Kazuo Sasaki¹

^* Department of Bio-Information Engineering, Faculty of Engineering, Toyama University, Toyama 930-8555, Japan;
Foundation for Oriental Medicine Research, Tokyo, Japan; and
Department of Physiology, Faculty of Medicine, Kyushu University, Fukuoka 882-0066, Japan

Abstract

Leptin, a product of the ob gene, decreases food intake and body weight in both Wistar and Zucker obese rats when administered centrally or peripherally. To examine whether these leptin effects might be mediated through a neuropeptide Y (NPY) signaling pathway in the medial part of the arcuate nucleus of the hypothalamus (vmARC), the effects of leptin on vmARC neurons in Wistar and Zucker obese rats were examined electrophysiologically using brain slice preparations. Bath application of leptin inhibited about 60% of the vmARC neurons recorded in slices from Wistar rats. Similar inhibitory effects of leptin on vmARC neurons were also observed under low-Ca²⁺, high-Mg²⁺ Ringer’s solution. However, inhibitory effects were almost absent under Ringer’s solution containing a protein kinase C inhibitor, chelerythrine chloride. In slices from Zucker obese rats, leptin inhibited only about 25% of the vmARC neurons recorded, and the proportion of neurons inhibited was significantly smaller for these rats than for Wistar rats. These results suggest that reductions in food intake and body weight induced by leptin in both Wistar and Zucker obese rats are partly mediated via inhibition of an NPY signaling pathway in the vmARC.

Key Words: leptin • arcuate nucleus • protein kinase C • Wistar rat • Zucker rat

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