Linalool from rosewood (Aniba rosaeodora Ducke) oil inhibits adenylate cyclase in the retina, contributing to understanding its biological activity.

Phytother Res

Laboratório de Bioquímica do Desenvolvimento do Sistema Nervoso, Instituto de Ciências Biológicas, Universidade Federal do Pará, 66075-110 Belém, PA, Brazil.

Published: January 2012

AI Article Synopsis

  • Rosewood oil (RO) contains linalool, a compound known for its anti-anxiety, sedative, and anticonvulsant properties, which may help protect against seizures by inhibiting cAMP increases.
  • The study aimed to evaluate the effects of RO and its linalool variants on adenylate cyclase activity in chick retinas, using forskolin to stimulate enzyme activity and measuring cAMP accumulation.
  • Results showed that RO and linalool compounds inhibited cAMP accumulation triggered by forskolin, indicating different relative efficacies among them and furthering the understanding of linalool's relaxing effects on the central nervous system.

Article Abstract

Rosewood oil (RO) (Aniba rosaeodora Ducke) is rich in linalool, a monoterpene alcohol, which has well studied anxiolytic, sedative and anticonvulsant effects. The inhibition of the increases in cAMP protects against seizures in a diversity of models of epilepsy. In this paper, the principal aim was to investigate the effects of RO, (±)-linalool and (-)-linalool) on adenylate cyclase. They were tested in chick retinas and forskolin was used to stimulate the enzyme target. The phosphodiesterase inhibitor, 4-(3-butoxy-4-methoxybenzyl)-imidazolidin-2-one, and the non-selective adenosine receptor antagonist 3-isobutyl-methyl-xanthine (IBMX), were used to control the participation of phosphodiesterase and adenosine receptors in the resulting effects, respectively. The cAMP accumulation was measured by enzyme immune assay (EIA). Rosewood oil, (-)-linalool and (±)-linalool inhibited exclusively the cAMP accumulation stimulated by forskolin, even when adenosine receptors were blocked with IBMX. The IC(50) values (in μ m concentration range) calculated from their concentration response-curves were not statistically different, however, the compounds presented a different relative efficacy. These results extend the range of subcellular mechanisms underlying the relaxant action of linalool on the central nervous system.

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Source
http://dx.doi.org/10.1002/ptr.3518DOI Listing

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