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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Gabaculine is a naturally occurring neurotoxin first isolated from the bacteria Streptomyces toyacaensis, which acts as a potent and irreversible GABA transaminase inhibitor, and also a GABA reuptake inhibitor. Gabaculine is also known as 3-amino-2,3-dihydrobenzoic acid hydrochloride and 5-amino cyclohexa-1,3 dienyl carboxylic acid. Gabaculine increased GABA levels in the brain and had an effect on convulsivity in mice.
Mechanism of Action
Gabaculine includes a comparable structure to GABA and a dihydrobenzene ring. This comparable GABA structure is used in order to be able to take the place of GABA during the first steps of transamination, including transaldimination and 1,3-prototrphic shift to the pyridoxamine imine. Following this, a proton from the dihydrobenzene ring is abstracted by an enzymatic base, thus causing the ring to become aromatic. The aromatic stabilization energy of the aromatic ring is what causes this reaction to be irreversible, thus causing the complex not to react further.
Animal studies to determine the effect of gabaculine on GABA levels in the brain were heavily conducted around the 1970s. These in vivo studies involved mostly the use of mice that underwent intravenous administration of this drug. Each of these studies concluded that gabaculine has a great potential to increase the GABA levels in the brain of these mice in a time dependent manner. Along with determining the effect of GABA levels, in vivo studies were conducted to investigate the ability of gabaculine to inhibit convulsions in mice. Results indicated that gabaculine provided a clear anticonvulsant effect against seizures induced by high doses of chemoconvulsants or electroshock. The toxicity of this compound was also investigated using animal mouse models. This study showed that at anticonvulsant doses, gabaculine is extremely potent and toxic when compared to other GABA transaminase inhibitors, with an ED50 of 35 mg/kg and LD50 of 86 mg/kg. Because of this potential lethal effect, gabaculine was proved to be too toxic for use as a drug however, it can still be used as a compound to alter GABA levels in studies of experimental epilepsy.
Chemical Product and Regulation
Gabaculine has not been found to be approved by the FDA as a pharmaceutical entity; however, it can be used as a chemical compound for research purposes only. A gabaculine material safety and data sheet from Santa Cruz Biotechnology indicates that this compound is not considered a hazardous substance according to OSHA 29 CFR 1910.1200.
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- Santa Cruz Biotechnology, Inc. "Gabaculine Material Safety Data Sheet". Retrieved 5 December 2014.
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- Rando, Robert; Bangerter, F.W. (May 13, 1977). "The In Vivo Inhibition of GABA-transaminase by Gabaculine" (PDF). BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS. 76 (4). doi:10.1016/0006-291X(77)90993-7. Retrieved 3 December 2014.
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- PubChem. "Gabaculine". http://pubchem.ncbi.nlm.nih.gov/. National Center for Biotechnology Information. Retrieved 9 December 2014. External link in