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Chronic intracerebroventricular infusion of insulin failed to alter brain insulin-binding sites, food intake, and body weight.

作者信息

Manin M, Balage M, Larue-Achagiotis C, Grizard J

机构信息

Laboratoire d'Etude du Métabolisme Azoté, INRA Clermont-Theix, Ceyrat, France.

出版信息

J Neurochem. 1988 Dec;51(6):1689-95. doi: 10.1111/j.1471-4159.1988.tb01146.x.

Abstract

The present study was performed to explore the role of exogenous insulin in CSF in the control of energy balance in the rat. For this purpose, adult male Sprague-Dawley rats carrying an indwelling cannula in the right lateral cerebral ventricle were infused for a maximum of 10 days with insulin (Actrapid) at various rates (starting at 0, 45, 85, 170, and 600 ng/day) or anti-insulin antibody (IgG fraction; diluted 1:10 wt/vol) with an osmotic minipump. All those treatments did not modify the growing rates; neither total daily food intake nor the circadian rhythm of food intake was further modified. The chronic insulin infusion starting at 600 ng/day resulted in a chronic significant increase in CSF insulin levels without changing the plasma insulin level. It failed to alter specific insulin binding sites to Triton X-100 solubilized microsomal membranes from various brain areas (cerebral cortex, olfactory bulbs, and lateral and medial hypothalami) at the end of the 5- or 10-day period of insulin infusion. Purification of insulin receptors on a wheat germ agglutinin did not reveal any further effect of insulin. From these results, it seems unlikely that the input to the brain insulin-effector systems could arise from CSF insulin.

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