## Abstract Pharmacological characterization of the action of the novel non‐N‐methyl‐D‐aspartate non‐NMDA) antagonist AMOA (2‐amino‐3‐[3‐ (carboxymethoxy)‐5‐methylisoxazol‐4‐yl]propionate on glutamate receptors was investigated in __Xenopus__ ooccytes injected with mouse brain mRNA. AMOA (150 μM) p
Histamine effects on the 5-HT1c receptor expressed in Xenopus oocytes
✍ Scribed by S. Shichijo; D. G. Payan; G. Harrowe; Dr.; M.D. M. Mitsuhashi
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 478 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0360-4012
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✦ Synopsis
Abstract
To analyze the cross‐reactivity between serotonin (5‐HT) and histamine, the in vitro transcribed RNA for the 5‐HT~1c~ receptor was functionally expressed in Xenopus oocytes. 5‐HT significantly increased ^45^Ca^2+^ efflux in RNA‐injected oocytes, but not in uninjected and water‐injected control oocytes. Furthermore, histamine and the H~1~ receptor agonists, but not the H~2~ and H~3~ agonists, significantly induced ^45^Ca^2+^ efflux in 5‐HT1c receptor RNA‐injected oocytes, but not in uninjected and water‐injected oocytes. However, the H~1~, H~2~, and H~3~ antagonists failed to inhibit histamine‐induced ^45^Ca^2+^ efflux at 10^−6^M. This finding suggests that the 5‐HT~1c~ receptor can be activated by both 5‐HT and histamine, although the action of histamine is different from classic histamine pharmacology.
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