Abstract
Carp were cannulated in the dorsal aorta, and after 2 days of recovery they were infused with 1) norepinephrine, 2) yohimbine (alpha(2)-antagonist) plus norepinephrine, 3) clonidine (alpha(2)-agonist), and 4) isoproterenol (nonselective beta-agonist). Norepinephrine lowered the plasma free fatty acid (FFA) level and raised the plasma glucose level for several hours. Norepinephrine in combination with the alpha(2)-antagonist yohimbine resulted in retardation of the FFA decrease, indicating the involvement of alpha(2)-adrenoceptors. Infusion with the partial alpha(2)-agonist clonidine had a smaller effect. Infusion with isoproterenol caused a marked increase of glucose levels, and unexpectedly a decline of plasma FFA levels, indicating a direct involvement of beta-adrenoceptors. Combination of isoproterenol with either atenolol (beta(1)-antagonist) or ICI-118,551 (beta(2)-antagonist) showed that both beta(1)- and beta(2)-adrenoceptors were involved in the glucose release by isoproterenol. Remarkably, the decline of FFA levels was augmented in the presence of ICI-118,551, whereas with atenolol present plasma FFA levels were increased by isoproterenol. Thus it is concluded that in carp both beta(1)- and beta(2)-adrenoceptors mediate glucose release, whereas lipolysis is controlled by inhibitory beta(1)-adrenoceptors and stimulatory beta(2)-adrenoceptors, as well as by inhibitory alpha(2)-adrenoceptors.
Original language | English |
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Pages (from-to) | R615-24 |
Journal | American Journal of Physiology. Regulatory Integrative and Comparative Physiology |
Volume | 281 |
Issue number | 2 |
Publication status | Published - Aug 2001 |
Keywords
- Adrenergic Agonists
- Adrenergic alpha-Agonists
- Adrenergic alpha-Antagonists
- Adrenergic beta-Agonists
- Adrenergic beta-Antagonists
- Animals
- Atenolol
- Blood Glucose
- Carps
- Clonidine
- Epinephrine
- Fatty Acids, Nonesterified
- Isoproterenol
- Lactic Acid
- Norepinephrine
- Propanolamines
- Receptors, Adrenergic, beta
- Yohimbine
- Journal Article