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The antinociceptive effect of intracerebroventricularly administered prostaglandin D2in the rat

✍ Scribed by S. K. Bhattacharya


Publisher
Springer
Year
1986
Tongue
English
Weight
434 KB
Volume
89
Category
Article
ISSN
0033-3158

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✦ Synopsis


Intracerebroventricular administration of prostaglandin D2 (PGD2), the major PG in the rat brain, produced a dose-related anti-nociceptive effect in rats as assessed by the rat tail-hot wire, hot plate and phenylquinoneinduced writhing techniques. The antinociceptive action of centrally-administered PGD2 was markedly attenuated after pretreatment of the rats with 5,6-dihydroxytryptamine, a selective neurotoxin for central serotonergic neurones, and p-chlorophenylalanine, a specific inhibitor of serotonin synthesis, indicating that the PGD2 action is serotonin-mediated. Naloxone, an antagonist of endogenous opioid receptors, also antagonised the antinociceptive action of PGD2. Earlier reports from this laboratory have shown that the antinociceptive action of centrally-administered PGE1 in rats is a serotonin-mediated effect and is also antagonised by naloxone. It was further shown that PGD2, like PGE1, augments serotonin turnover in the rat brain. The present findings support the view that PGD2 shares some of the central actions of PGEs and, like the latter, may function as a neuromodulator in the central nervous system.


πŸ“œ SIMILAR VOLUMES


The antinociceptive effect of intracereb
✍ A. K. Sanyal; D. N. Srivastava; S. K. Bhattacharya πŸ“‚ Article πŸ“… 1979 πŸ› Springer 🌐 English βš– 394 KB

It is generally accepted that prostaglandins (PGs) are nociceptive substances. However, earlier studies from this laboratory indicated that morphine analgesia, in the rat, was not only serotonin mediated, but involved PGs as well. Several PG synthesis inhibitors were shown to inhibit morphine analge