z-logo
open-access-imgOpen Access
Changes of brain neuropeptide Y and its receptors in rats with flurazepam tolerance and dependence 1
Author(s) -
ZHANG Liping,
WANG Li
Publication year - 2005
Publication title -
acta pharmacologica sinica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.514
H-Index - 90
eISSN - 1745-7254
pISSN - 1671-4083
DOI - 10.1111/j.1745-7254.2005.00179.x
Subject(s) - receptor , neuropeptide , neuropeptide y receptor , flurazepam , pharmacology , neuroscience , medicine , chemistry , biology , benzodiazepine
Aim: Anticonvulsant tolerance and dependence are two obstacles that restrict the clinical use of benzodiazepines (BDZ). In order to explore the mechanism of these two adverse reactions, changes of neuropeptide Y (NPY) and its receptors in the hippocampus of rat models, in relation to flurazepam (FZP, a member of BDZ) tolerance and dependence, were investigated. Methods: The mRNA of preproNPY and its receptors (Y 1 , Y 2 , and Y 5 ) in the hippocampus were determined by competitive RT‐PCR, and the distribution of NPY in the hippocampus was examined by immunohistochemistry. Results: A decrease of preproNPY mRNA in the hippocampus was found in tolerant and dependent rats. The level of preproNPY mRNA in the hippocampus was reversely correlated with the degree of tolerance and dependence, measured by the threshold of pentylenetetrazol‐induced seizures. Immunohistochemistry indicated a decrease of NPY‐immunoreactive material in neurons of the CA1, CA3, and dentate gyrus regions of both tolerant and dependent rats. The mRNA of NPY receptors Y 1 and Y 5 decreased in tolerant rats but did not change in dependent rats. The mRNA of NPY receptor Y 2 increased in tolerant rats but decreased in dependent rats. Conclusion: A decrease of NPY in the hippocampus might be involved in anticonvulsant tolerance and dependence following long‐term treatment with FZP. Y 1 Y 2 , and Y 5 mRNA were also altered in FZP tolerance and dependence.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here