Alterations in insulin and glucagon secretion by monosodium glutamate lesions of the hypothalamic arcuate nucleus.

This study was performed to determine the effects of monosodium glutamate (MSG) induced lesions of the hypothalamic arcuate nucleus (ARC) on glucose tolerance and insulin and glucagon secretion in male golden hamsters. Eight day old hamsters were given a single s.c. injection of 5.8 mg/g BW MSG or hypertonic saline (controls). Studies were initiated when the hamsters were 3 months of age. At this age there were no body weight differences. Glucose (180 mg/100 g BW) was administered via stomach tube to 18 control and 18 MSG-treated hamsters. Animals were anesthetized with ether and a single blood sample from the portal vein was taken either before or at 30 or 60 min after glucose administration (n = 6/group). Glucose concentrations were similar in both groups at all time periods. Insulin concentrations in the MSG group were significantly (P less than 0.05) elevated in MSG-treated hamsters compared to controls at the 60 min time point. Glucose suppressed glucagon (P less than 0.05) in control but not in MSG-treated hamsters. The MSG group had significantly more glucagon (P less than 0.05) in portal vein blood at 30 min after glucose administration than did the control hamsters. Molar insulin/glucagon ratios did not differ between the 2 groups which likely accounts for the lack of differences in blood glucose levels. These results suggest a role for the ARC in regulating pancreatic function.