Ionotropic GABA receptor

Ionotropic GABA receptors (iGABARs) are ligand-gated ion channel GABA receptors and include:

The GABAB receptor, a G protein-coupled receptor, is the only metabotropic GABA receptor.

They belong to a larger class of GABA receptors which are known for their inhibitory effects on postsynaptic cells. There are physiological differences between the ionotropic and metabotropic GABA receptors.There are pharmacological implications in characterizing iGABAR receptors.

Introduction
This is a neuromuscular junction. There is a presynaptic unit (axon), a synapse and a postsynaptic unit (dendrite). Neurotransmitters are released into the synapse.

The neuromuscular junction in the CNS can be composed of a presynaptic unit located at an axon terminal with synaptic vesicles and a postsynaptic unit located at a dendrite.[1] Neurotransmitters are chemical molecules that are released from a presynaptic unit into the synapse and received by the postsynaptic unit, resulting in a biological and electrophysiological effect. The two main types of neurotransmitters are amino acid transmitters and GABA transmitters.[1] The release of and binding of glutamate, an amino acid transmitter, to its respective receptor manifests in an excitatory postsynaptic potential (EPSP).[1] On the other hand, the release and binding of gamma-amino butyric acid (GABA) to the GABA receptor results in an inhibitory postynaptic potential (IPSP).[1] The ability of the GABA receptor function rests on its molecular structure of multiple binding sites and conductance levels.[1] These receptors are prevalent in interneurons relaying messages among various regions of the brain.[1]

The Difference Between Ionotropic and Metabotropic GABA receptors
Classification of Ligand-Gated Ion Channels: iGABARs fall under the Cys-Loop receptors.

The two types of GABA receptors are the GABAA and GABAB receptors. The pentameric GABAA receptors are ionotropic, meaning that upon binding with the ligand their biological and electrophysiological effect is carried out through the conductance of ions.[2] This is why the physiological makeup for GABAA receptors differs from GABAB in that they are ligand-gated ion channels. The chloride-ion gated channels facilitate the inhibitory effect through the influx of chloride ions.[2] However, GABAB receptors are metabotropic meaning they utilize a G-protein coupled mechanism. Since the G-protein is a heterodimeric[2] molecule, the separation and phosphorylation of its parts result in a signal cascade, resulting in a more steady but amplified response. 

Pharmacological Implications

Earlier a third type of GABA receptor was discovered and named GABAC, but recently it has been categorized as a sub-type of the GABAA receptor.[3] Thus, the iontropic GABA receptors consist of the GABAA receptor and the GABAA-ρ receptor.There are pharmacological implications in understanding the molecular structure and function of these ionotropic receptors. Since they are targeted by neuroactive drugs, this characteristic is exploited in order to deduce their molecular structure and function in the CNS.[4] For example, GABAA receptors respond to neuroactive drugs like bensodiazepines.[5] Normally increasing a neuron's permeability to chloride ions results in inhibition; bensodiazepines further propagate this event ensuring inhibition, serving as an indirect[5] factor. Armed with the knowledge of chloride ion permeability leading to inhibition, it is important to note that ethanol and barbiturates[5] can directly increase the influx of chloride ions resulting in inhibition. Further characterization of the allosteric modulations[2] of the active sites in the ionotropic gives insight on new treatments and nervous system disorders, such as panic disorder.[6]

References
  1. Shepherd GM, Hanson PI (2014). "Synaptic transmission". AccessScience. McGraw-Hill Education. doi:10.1036/1097-8542.674100.
  2. Enna SJ, Möhler H (2007). The GABA receptors. Humana Press. OCLC 474809970.
  3. Bormann J (January 2000). "The 'ABC' of GABA receptors". Trends in Pharmacological Sciences. 21 (1): 16–9. doi:10.1016/S0165-6147(99)01413-3. PMID 10637650.
  4. Palyulin VA, Radchenko EV, Osolodkin DE, Chupakhin VI, Zefirov NS (May 2010). "Ionotropic GABA receptors: modelling and design of selective ligands". Journal of Cheminformatics. 2 (S1). doi:10.1186/1758-2946-2-s1-p49.
  5. Carlton PL (2014). "Tranquilizer". AccessScience. McGraw-Hill Education. doi:10.1036/1097-8542.704300.
  6. Stein DJ, Carey PD (2020). "Anxiety disorders". AccessScience. McGraw-Hill Education. doi:10.1036/1097-8542.042250.
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