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Pharmacological Characterization of Sigma Binding Sites in Guinea Pig Brain Membranes

  • E. W. Karbon
  • S. J. Enna
Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 287)

Abstract

The pharmacological, biochemical and behavioral characterization of sigma binding sites is currently the focus of intense investigation. First described by Martin and his colleagues (1976) to account for the behavioral effects of selected benzomorphan opiates, sigma binding sites were originally classified as an opioid receptor subtype. Subsequent work suggested this designation was inaccurate since, unlike opioid receptors, the sigma site is insensitive to blockade by naloxone (Itzhak et al., 1985; Katz et al., 1985). In addition, the (+) isomers of opiates such as pentazocine and N-allylnormetazocine (SKF 10,047) are more active at sigma binding sites, while opiate receptors are typically more responsive to (-) isomers (Weber et al., 1986).

Keywords

Sigma Receptor Haloperidol Administration Sigma Ligand Opioid Receptor Subtype Sigma Binding 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Plenum Press, New York 1991

Authors and Affiliations

  • E. W. Karbon
    • 1
  • S. J. Enna
    • 1
  1. 1.Nova Pharmaceutical CorporationBaltimoreUSA

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