We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.
To save content items to your account,
please confirm that you agree to abide by our usage policies.
If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account.
Find out more about saving content to .
To save content items to your Kindle, first ensure no-reply@cambridge.org
is added to your Approved Personal Document E-mail List under your Personal Document Settings
on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part
of your Kindle email address below.
Find out more about saving to your Kindle.
Note you can select to save to either the @free.kindle.com or @kindle.com variations.
‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi.
‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
from
Part V
-
Specific psychotropic drugs and disorders
By
Smita A. Pandit, Psychopharmacology Unit, School of Medical Sciences, Bristol, UK,
Spilios V. Argyropoulos, Psychopharmacology Unit, School of Medical Sciences, Bristol, UK,
Patrick G. Kehoe, Psychopharmacology Unit, School of Medical Sciences, Bristol, UK,
David J. Nutt, Psychopharmacology Unit, School of Medical Sciences, Bristol, UK
Edited by
Bernard Lerer, Hadassah-Hebrew Medical Center, Jerusalem
The benzodiazepines (BDZ) have proven to be both effective and controversial in the treatment of anxiety. New insights into the genetics of the BD2 receptor system may lead to the development of new drugs that act on the γ-aminobutyric acid (GABA) receptor complex and are devoid of the problems associated with the classical BDZs. This pharmacotherapeutic approach has gathered impetus following the discovery of the various subunits of the GABA receptor, which play an important role in the regulation of anxiety and the actions of anxiolytics, and which demonstrate differential brain expression. This chapter discusses the above with reference to recent evidence from animal and human studies, as well as the implications for future anxiolytic treatment strategies. It focuses on the development of the GABA-BDZ receptor field of research. Unlike the BDZ site, the modulation of the GABA receptor by neurosteroids requires the presence of a β-subunit.
Recommend this
Email your librarian or administrator to recommend adding this to your organisation's collection.