Abstract
A gender difference in the glucagon response to insulin-induced hypoglycemia was previously demonstrated in humans. Whether this reflects a gender difference in autonomic activation or in pancreatic alpha-cell regulation is not known. We investigated the glucagon, epinephrine, and norepinephrine responses to neuroglycopenic stress induced by 2-deoxy-D-glucose (2-DG) or insulin in female and male mice. 2-DG increased plasma glucagon levels by 559 +/- 68% in females versus 281 +/- 46% in males (P < 0.01). Plasma levels of epinephrine or norepinephrine after 2-DG administration did not differ between genders. During insulin-induced hypoglycemia, the glucagon response was similarly higher in females (P < 0.001), whereas the plasma catecholamine response was higher in males (P < 0.05). In vivo, the glucagon response to carbachol or clonidine was higher in females (P < 0.05). In isolated islets, the glucagon response to carbachol (100 microM; P = 0.003) but not to clonidine (1 microM) was larger in females. We conclude that in addition to a larger alpha-cell mass (previously described in female mice), an increased sensitivity of the glucagon-producing alpha-cell to cholinergic activation contributes to the larger glucagon response to glucopenic stress in female mice.
Original language | English |
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Pages (from-to) | R281-R288 |
Journal | American Journal of Physiology: Regulatory, Integrative and Comparative Physiology |
Volume | 282 |
Issue number | 1 |
Publication status | Published - 2002 |
Subject classification (UKÄ)
- Other Clinical Medicine
Free keywords
- Sympatholytics : pharmacology
- Stress : metabolism
- Sex Characteristics
- Norepinephrine : blood
- Mice Inbred Strains
- Mice
- Male
- Islets of Langerhans : drug effects : physiology : secretion
- Insulin : pharmacology
- Hypoglycemic Agents : pharmacology
- Female
- Glucagon : blood : secretion
- Hypoglycemia : chemically induced : metabolism
- Epinephrine : blood
- Clonidine : pharmacology
- Deoxyglucose : pharmacology
- Support Non-U.S. Gov't
- Cholinergic Agonists : pharmacology
- Carbachol : pharmacology
- Blood Glucose : metabolism
- Autonomic Nervous System : metabolism
- Antimetabolites : pharmacology
- Animal
- Adrenal Glands : physiology