Abstract
1. Octopamine (OA) (10(-7)-10(-5) M) relaxed isolated foreguts. Tyramine mimicked the effects of OA but was 64x less potent. 2. Proctolin (10(-8) M to 10(-6) M) induced contraction of isolated foreguts was antagonised non competitively by tyramine. 3. Mianserin (10(-6) M) was a non competitive antagonist of relaxation caused by tyramine but was without effect on proctolin induced contraction. 4. Caffeine (1 microM and 2 microM) caused non competitive inhibition of proctolin-induced tissue contraction. 5. It is concluded that tyramine antagonises proctolin-induced contraction of the foregut by activating an adenylate cyclase-linked OA2 receptor.
Original language | English |
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Pages (from-to) | 233-6 |
Number of pages | 4 |
Journal | Comparative Biochemistry and Physiology. C, Comparative Pharmacology and Toxicology |
Volume | 95 |
Issue number | 2 |
DOIs | |
Publication status | Published - 1990 |
Keywords
- Animals
- Caffeine/pharmacology
- Digestive System/drug effects
- Digestive System Physiological Phenomena
- Dose-Response Relationship, Drug
- Female
- Grasshoppers/physiology
- Male
- Mianserin/pharmacology
- Muscle Contraction/drug effects
- Muscle, Smooth/drug effects
- Neuropeptides
- Octopamine/pharmacology
- Oligopeptides/antagonists & inhibitors
- Receptors, Adrenergic/metabolism
- Receptors, Biogenic Amine
- Tyramine/pharmacology