Goldberg Joel S
Durham Veterans Affairs Medical Center and Duke University School of Medicine Durham, NC, USA.
Perspect Medicin Chem. 2010 Aug 3;4:23-31. doi: 10.4137/pmc.s5490.
Central pain is an enigmatic, intractable condition, related to destruction of thalamic areas, resulting in likely loss of inhibitory synaptic transmission mediated by GABA. It is proposed that treatment of central pain, a localized process, may be treated by GABA supplementation, like Parkinson's disease and depression. At physiologic pH, GABA exists as a zwitterion that is poorly permeable to the blood brain barrier (BBB). Because the pH of the cerebral spinal fluid (CSF) is acidic relative to the plasma, ion trapping may allow a GABA ester prodrug to accumulate and be hydrolyzed within the CSF. Previous investigations with ester local anesthetics may be applicable to some GABA esters since they are weak bases, hydrolyzed by esterases and cross the BBB. Potential non-toxic GABA esters are discussed. Many GABA esters were investigated in the 1980s and it is hoped that this paper may spark renewed interest in their development.
中枢性疼痛是一种神秘且难以治疗的病症,与丘脑区域的破坏有关,可能导致由γ-氨基丁酸(GABA)介导的抑制性突触传递丧失。有人提出,中枢性疼痛作为一种局部性病症,其治疗方法可能与帕金森病和抑郁症一样,通过补充GABA来进行。在生理pH值下,GABA以两性离子形式存在,难以透过血脑屏障(BBB)。由于相对于血浆,脑脊液(CSF)的pH呈酸性,离子捕获可能使GABA酯前药在脑脊液中积累并水解。以往对酯类局部麻醉剂的研究可能适用于某些GABA酯,因为它们是弱碱,可被酯酶水解并穿过血脑屏障。本文讨论了潜在的无毒GABA酯。20世纪80年代对许多GABA酯进行了研究,希望本文能重新激发人们对其开发的兴趣。