GABAA-rho receptor: Difference between revisions - Wikipedia


Article Images

Content deleted Content added

Line 67:

== Function ==

In addition to containing a GABA binding site, the GABA<sub>A</sub>-ρ receptor complex conducts [[chloride]] ions across neuronal [[cell membrane|membrane]]s. Binding of GABA to the receptor results in opening of this channel. When the [[reversal potential]] of chloride is less than the membrane potential, chloride ions flow down their [[electrochemical gradient]] into the cell. This influx of chloride ions lowers the [[membrane potential]] of (hyperpolarizes) the neuron, making it more difficult for these cells to conduct electrical impulses in the form of an action potential. Following stimulation by GABA, the chloride current produced by GABA<sub>A</sub>-ρ receptors is slow to initiate but sustained in duration. In contrast, the GABA<sub>A</sub> receptor current has a rapid onset and short duration. GABA is about 10 times more potent at GABA<sub>A</sub>-ρ than it is at most GABA<sub>A</sub> receptors.<ref name="Martin">{{cite web | url = http://www.tocris.com/pdfs/gabarev.pdf | title = A review of GABA and the receptors to which it binds | author = Martin IL, Dunn SJM | authorlink = | coauthors = | date = 2002-03-01 | format = | work = Tocris Reviews No. 20 | publisher = Tocris Cookson Ltd., UK | pages = | language = | archiveurl = | archivedate = | quote = | accessdate = 2009-05-17}}</ref>

== Structure ==

Line 108:

== Genetics ==

In humans, GABA<sub>A</sub>-ρ receptor subunits ρ1 and ρ2 are [[code for|encoded by]] the {{Gene|GABRR1}} and {{Gene|GABRR2}} [[gene]]s which are found on [[Chromosome 6 (human)|chromosome 6]] whereas the {{Gene|GABRR3}} gene for ρ3 is found on [[Chromosome 3 (human)|chromosome 3]].<ref name="Martin"/> Mutations in the ρ1 or ρ2 genes may be responsible for some cases of [[autosomal recessive]] [[retinitis pigmentosa]].<ref name="Marcos">{{cite journal |author=Marcos I, Ruiz A, Blaschak CJ, Borrego S, Cutting GR, Antinolo G|title=Mutation analysis of GABRR1 and GABRR2 in autosomal recessive retinitis pigmentosa|journal= J Med Genet |volume= 37 |issue= 6 |pages= E5 |year= 1998 |pmid= 10851258 |pmc=1734609 | doi = 10.1136/jmg.37.6.e5}}</ref>

== References ==