Effect of arachidonic acid on specific binding of [H-3]naloxone to opioid receptors

Date

2000-01-01

Author

Apaydin, S
Öktem, Hüseyin Avni

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The effects of arachidonic acid (AA) on binding of [H-3]naloxone to the agonist and antagonist configurations of opioid receptors were investigated in rat brain. Equilibrium binding parameters of the agonist and antagonist configurations of the receptors were evaluated from homologue displacement data in the presence or absence of AA. Addition of AA at a concentration of 0.6 mM (1.5 mu mole/mg of protein) reduced by 22% and 53% the maximal number of binding sites (B-max) respectively in the absence or presence of 100 mM NaCl. Binding affinity (K-D) was not altered significantly (P<0.05) either in the presence or absence of 100 mM NaCl and AA. We conclude that AA mediated reduction in [H-3]naloxone specific binding was chiefly due to a decrease in the number of binding sites.

Subject Keywords

Arachidonic acid, Opioid receptors, [H-3]naloxone binding

URI

https://hdl.handle.net/11511/55012

Journal

ACTA NEUROBIOLOGIAE EXPERIMENTALIS

Collections

Department of Biology, Article

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Citation Formats

S. Apaydin and H. A. Öktem, “Effect of arachidonic acid on specific binding of [H-3]naloxone to opioid receptors,” ACTA NEUROBIOLOGIAE EXPERIMENTALIS, pp. 361–363, 2000, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/55012.