GABA A Receptor Density Is Not Altered by a Novel Herbal Anxiolytic Treatment
Anxiety disorders are highly prevalent and considered a major public health concern worldwide. Current anxiolytics are of limited efficacy and associated with various side effects. Our novel herbal treatment (NHT), composed of four constituents, was shown to reduce anxiety-like behavior while preclu...
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creator | Doron, Ravid Sever, Avital Handelsman, Assaf Toledano, Roni Franko, Motty Hirshler, Yafit Shamir, Alon Burstein, Or Rehavi, Moshe |
description | Anxiety disorders are highly prevalent and considered a major public health concern worldwide. Current anxiolytics are of limited efficacy and associated with various side effects. Our novel herbal treatment (NHT), composed of four constituents, was shown to reduce anxiety-like behavior while precluding a common side effect caused by current anxiolytics, i.e., sexual dysfunction. Nevertheless, NHT's mechanism of action is yet to be determined. There is evidence that some medicinal herbs interact with the GABAergic system. Therefore, we aimed to examine whether NHT's anxiolytic-like effect is exerted by alterations in GABA
receptor density in the hippocampus, prefrontal cortex, and hypothalamus. The effects of 3-weeks treatment with NHT on anxiety-like behavior and locomotion were assessed using the elevated plus maze (EPM) and the open field test (OFT), respectively. Regional GABA
receptor levels were analyzed using [
H] RO15-1788 high-affinity binding assays. In stressed mice, NHT reduced anxiety-like behavior similarly to the benzodiazepine, clonazepam, while locomotion remained intact. Lack of changes or minor changes in regional GABA
receptor density in the brain were induced by NHT or clonazepam. In naive mice, performance in the EPM, locomotion and GABA
receptor densities were not altered by treatment with NHT or clonazepam. These findings support NHT as an efficacious and safe anxiolytic, although the GABAergic involvement remains to be further elucidated. |
doi_str_mv | 10.1007/s12031-018-1078-2 |
format | Article |
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receptor density in the hippocampus, prefrontal cortex, and hypothalamus. The effects of 3-weeks treatment with NHT on anxiety-like behavior and locomotion were assessed using the elevated plus maze (EPM) and the open field test (OFT), respectively. Regional GABA
receptor levels were analyzed using [
H] RO15-1788 high-affinity binding assays. In stressed mice, NHT reduced anxiety-like behavior similarly to the benzodiazepine, clonazepam, while locomotion remained intact. Lack of changes or minor changes in regional GABA
receptor density in the brain were induced by NHT or clonazepam. In naive mice, performance in the EPM, locomotion and GABA
receptor densities were not altered by treatment with NHT or clonazepam. These findings support NHT as an efficacious and safe anxiolytic, although the GABAergic involvement remains to be further elucidated.</description><identifier>EISSN: 1559-1166</identifier><identifier>DOI: 10.1007/s12031-018-1078-2</identifier><identifier>PMID: 29737465</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Anti-Anxiety Agents - pharmacology ; Anti-Anxiety Agents - therapeutic use ; Anxiety - drug therapy ; Anxiety - metabolism ; Brain - drug effects ; Brain - metabolism ; Clonazepam - pharmacology ; Clonazepam - therapeutic use ; Male ; Maze Learning ; Mice ; Mice, Inbred C57BL ; Plant Extracts - pharmacology ; Plant Extracts - therapeutic use ; Receptors, GABA-A - genetics ; Receptors, GABA-A - metabolism</subject><ispartof>Journal of molecular neuroscience, 2018-05, Vol.65 (1), p.110</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-6523-9886</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29737465$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Doron, Ravid</creatorcontrib><creatorcontrib>Sever, Avital</creatorcontrib><creatorcontrib>Handelsman, Assaf</creatorcontrib><creatorcontrib>Toledano, Roni</creatorcontrib><creatorcontrib>Franko, Motty</creatorcontrib><creatorcontrib>Hirshler, Yafit</creatorcontrib><creatorcontrib>Shamir, Alon</creatorcontrib><creatorcontrib>Burstein, Or</creatorcontrib><creatorcontrib>Rehavi, Moshe</creatorcontrib><title>GABA A Receptor Density Is Not Altered by a Novel Herbal Anxiolytic Treatment</title><title>Journal of molecular neuroscience</title><addtitle>J Mol Neurosci</addtitle><description>Anxiety disorders are highly prevalent and considered a major public health concern worldwide. Current anxiolytics are of limited efficacy and associated with various side effects. Our novel herbal treatment (NHT), composed of four constituents, was shown to reduce anxiety-like behavior while precluding a common side effect caused by current anxiolytics, i.e., sexual dysfunction. Nevertheless, NHT's mechanism of action is yet to be determined. There is evidence that some medicinal herbs interact with the GABAergic system. Therefore, we aimed to examine whether NHT's anxiolytic-like effect is exerted by alterations in GABA
receptor density in the hippocampus, prefrontal cortex, and hypothalamus. The effects of 3-weeks treatment with NHT on anxiety-like behavior and locomotion were assessed using the elevated plus maze (EPM) and the open field test (OFT), respectively. Regional GABA
receptor levels were analyzed using [
H] RO15-1788 high-affinity binding assays. In stressed mice, NHT reduced anxiety-like behavior similarly to the benzodiazepine, clonazepam, while locomotion remained intact. Lack of changes or minor changes in regional GABA
receptor density in the brain were induced by NHT or clonazepam. In naive mice, performance in the EPM, locomotion and GABA
receptor densities were not altered by treatment with NHT or clonazepam. These findings support NHT as an efficacious and safe anxiolytic, although the GABAergic involvement remains to be further elucidated.</description><subject>Animals</subject><subject>Anti-Anxiety Agents - pharmacology</subject><subject>Anti-Anxiety Agents - therapeutic use</subject><subject>Anxiety - drug therapy</subject><subject>Anxiety - metabolism</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Clonazepam - pharmacology</subject><subject>Clonazepam - therapeutic use</subject><subject>Male</subject><subject>Maze Learning</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Extracts - therapeutic use</subject><subject>Receptors, GABA-A - genetics</subject><subject>Receptors, GABA-A - metabolism</subject><issn>1559-1166</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1j91KwzAYQIMgbk4fwBvJC0S_r0mT5rJO3QZTQeb1SNIvUOkfbRT79grq1YFzceAwdoVwgwDmdsIMJArAQiCYQmQnbIl5bgWi1gt2Pk3vABkqLM7YIrNGGqXzJXvalHclL_krBRpSP_J76qY6zXw38ec-8bJJNFLF_czdj_ikhm9p9K7hZfdV982c6sAPI7nUUpcu2Gl0zUSXf1yxt8eHw3or9i-b3brciwGhSMI4E6tcVZlDtEEpwNxjDBC9zLzRGpRGSz7YnIKFKIPEIhZKS-29itbJFbv-7Q4fvqXqOIx168b5-P8lvwGl4Exv</recordid><startdate>201805</startdate><enddate>201805</enddate><creator>Doron, Ravid</creator><creator>Sever, Avital</creator><creator>Handelsman, Assaf</creator><creator>Toledano, Roni</creator><creator>Franko, Motty</creator><creator>Hirshler, Yafit</creator><creator>Shamir, Alon</creator><creator>Burstein, Or</creator><creator>Rehavi, Moshe</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><orcidid>https://orcid.org/0000-0002-6523-9886</orcidid></search><sort><creationdate>201805</creationdate><title>GABA A Receptor Density Is Not Altered by a Novel Herbal Anxiolytic Treatment</title><author>Doron, Ravid ; Sever, Avital ; Handelsman, Assaf ; Toledano, Roni ; Franko, Motty ; Hirshler, Yafit ; Shamir, Alon ; Burstein, Or ; Rehavi, Moshe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p108t-7a7fd54d2a119c44015b1fc0fb32b76604619ebc95ec90f3c318f84636bb4f9a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Anti-Anxiety Agents - pharmacology</topic><topic>Anti-Anxiety Agents - therapeutic use</topic><topic>Anxiety - drug therapy</topic><topic>Anxiety - metabolism</topic><topic>Brain - drug effects</topic><topic>Brain - metabolism</topic><topic>Clonazepam - pharmacology</topic><topic>Clonazepam - therapeutic use</topic><topic>Male</topic><topic>Maze Learning</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Extracts - therapeutic use</topic><topic>Receptors, GABA-A - genetics</topic><topic>Receptors, GABA-A - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Doron, Ravid</creatorcontrib><creatorcontrib>Sever, Avital</creatorcontrib><creatorcontrib>Handelsman, Assaf</creatorcontrib><creatorcontrib>Toledano, Roni</creatorcontrib><creatorcontrib>Franko, Motty</creatorcontrib><creatorcontrib>Hirshler, Yafit</creatorcontrib><creatorcontrib>Shamir, Alon</creatorcontrib><creatorcontrib>Burstein, Or</creatorcontrib><creatorcontrib>Rehavi, Moshe</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Journal of molecular neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Doron, Ravid</au><au>Sever, Avital</au><au>Handelsman, Assaf</au><au>Toledano, Roni</au><au>Franko, Motty</au><au>Hirshler, Yafit</au><au>Shamir, Alon</au><au>Burstein, Or</au><au>Rehavi, Moshe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GABA A Receptor Density Is Not Altered by a Novel Herbal Anxiolytic Treatment</atitle><jtitle>Journal of molecular neuroscience</jtitle><addtitle>J Mol Neurosci</addtitle><date>2018-05</date><risdate>2018</risdate><volume>65</volume><issue>1</issue><spage>110</spage><pages>110-</pages><eissn>1559-1166</eissn><abstract>Anxiety disorders are highly prevalent and considered a major public health concern worldwide. Current anxiolytics are of limited efficacy and associated with various side effects. Our novel herbal treatment (NHT), composed of four constituents, was shown to reduce anxiety-like behavior while precluding a common side effect caused by current anxiolytics, i.e., sexual dysfunction. Nevertheless, NHT's mechanism of action is yet to be determined. There is evidence that some medicinal herbs interact with the GABAergic system. Therefore, we aimed to examine whether NHT's anxiolytic-like effect is exerted by alterations in GABA
receptor density in the hippocampus, prefrontal cortex, and hypothalamus. The effects of 3-weeks treatment with NHT on anxiety-like behavior and locomotion were assessed using the elevated plus maze (EPM) and the open field test (OFT), respectively. Regional GABA
receptor levels were analyzed using [
H] RO15-1788 high-affinity binding assays. In stressed mice, NHT reduced anxiety-like behavior similarly to the benzodiazepine, clonazepam, while locomotion remained intact. Lack of changes or minor changes in regional GABA
receptor density in the brain were induced by NHT or clonazepam. In naive mice, performance in the EPM, locomotion and GABA
receptor densities were not altered by treatment with NHT or clonazepam. These findings support NHT as an efficacious and safe anxiolytic, although the GABAergic involvement remains to be further elucidated.</abstract><cop>United States</cop><pmid>29737465</pmid><doi>10.1007/s12031-018-1078-2</doi><orcidid>https://orcid.org/0000-0002-6523-9886</orcidid></addata></record> |
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subjects | Animals Anti-Anxiety Agents - pharmacology Anti-Anxiety Agents - therapeutic use Anxiety - drug therapy Anxiety - metabolism Brain - drug effects Brain - metabolism Clonazepam - pharmacology Clonazepam - therapeutic use Male Maze Learning Mice Mice, Inbred C57BL Plant Extracts - pharmacology Plant Extracts - therapeutic use Receptors, GABA-A - genetics Receptors, GABA-A - metabolism |
title | GABA A Receptor Density Is Not Altered by a Novel Herbal Anxiolytic Treatment |
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