Johansson Maja, Strömberg Jessica, Ragagnin Gianna, Doverskog Magnus, Bäckström Torbjörn
Umeå Neurosteroid research center, Obstetrics and Gynecology, Clinical Sciences at Umeå University, Building 6M, 4th floor at NUS, SE-901 85 Umeå, Sweden; Umecrine Cognition AB, Sweden.
Umeå Neurosteroid research center, Obstetrics and Gynecology, Clinical Sciences at Umeå University, Building 6M, 4th floor at NUS, SE-901 85 Umeå, Sweden.
J Steroid Biochem Mol Biol. 2016 Jun;160:98-105. doi: 10.1016/j.jsbmb.2015.10.019. Epub 2015 Oct 30.
GABAA receptor modulating steroid antagonists (GAMSA) selectively inhibit neurosteroid-mediated enhancement of GABA-evoked currents at the GABAA receptor. 3α-hydroxy-neurosteroids, notably allopregnanolone and tetrahydrodeoxycorticosterone (THDOC), potentiate GABAA receptor-mediated currents. On the contrary, various 3β-hydroxy-steroids antagonize this positive neurosteroid-mediated modulation. Importantly, GAMSAs are specific antagonists of the positive neurosteroid-modulation of the receptor and do not inhibit GABA-evoked currents. Allopregnanolone and THDOC have both negative and positive actions. Allopregnanolone can impair encoding/consolidation and retrieval of memories. Chronic administration of a physiological allopregnanolone concentration reduces cognition in mice models of Alzheimer's disease. In humans an allopregnanolone challenge impairs episodic memory and in hepatic encephalopathy cognitive deficits are accompanied by increased brain ammonia and allopregnanolone. Hippocampal slices react in vitro to ammonia by allopregnanolone synthesis in CA1 neurons, which blocks long-term potentiation (LTP). Thus, allopregnanolone may impair learning and memory by interfering with hippocampal LTP. Contrary, pharmacological treatment with allopregnanolone can promote neurogenesis and positively influence learning and memory of trace eye-blink conditioning in mice. In rat the GAMSA UC1011 inhibits an allopregnanolone-induced learning impairment and the GAMSA GR3027 restores learning and motor coordination in rats with hepatic encephalopathy. In addition, the GAMSA isoallopregnanolone antagonizes allopregnanolone-induced anesthesia in rats, and in humans it antagonizes allopregnanolone-induced sedation and reductions in saccadic eye velocity. 17PA is also an effective GAMSA in vivo, as it antagonizes allopregnanolone-induced anesthesia and spinal analgesia in rats. In vitro the allopregnanolone/THDOC-increased GABA-mediated GABAA receptor activity is antagonized by isoallopregnanolone, UC1011, GR3027 and 17PA, while the effect of GABA itself is not affected.
γ-氨基丁酸A型(GABAA)受体调节性类固醇拮抗剂(GAMSA)可选择性抑制神经类固醇介导的GABAA受体上GABA诱发电流的增强。3α-羟基神经类固醇,尤其是别孕烯醇酮和四氢脱氧皮质酮(THDOC),可增强GABAA受体介导的电流。相反,各种3β-羟基类固醇可拮抗这种由神经类固醇介导的正向调节作用。重要的是,GAMSA是受体正向神经类固醇调节的特异性拮抗剂,并不抑制GABA诱发的电流。别孕烯醇酮和THDOC都具有负性和正性作用。别孕烯醇酮可损害记忆的编码/巩固和提取。在阿尔茨海默病小鼠模型中,长期给予生理浓度的别孕烯醇酮会降低认知能力。在人类中,别孕烯醇酮激发试验会损害情景记忆,在肝性脑病中,认知缺陷伴随着脑内氨和别孕烯醇酮水平的升高。海马切片在体外会因CA1神经元中别孕烯醇酮的合成而对氨产生反应,这会阻断长时程增强(LTP)。因此,别孕烯醇酮可能通过干扰海马LTP来损害学习和记忆。相反,用别孕烯醇酮进行药物治疗可促进神经发生,并对小鼠的痕迹眨眼条件反射的学习和记忆产生积极影响。在大鼠中,GAMSA UC1011可抑制别孕烯醇酮诱导的学习障碍,GAMSA GR3027可恢复肝性脑病大鼠的学习和运动协调能力。此外,GAMSA异别孕烯醇酮可拮抗大鼠中别孕烯醇酮诱导的麻醉作用,在人类中,它可拮抗别孕烯醇酮诱导的镇静作用和眼跳速度降低。17PA在体内也是一种有效的GAMSA,因为它可拮抗大鼠中别孕烯醇酮诱导的麻醉和脊髓镇痛作用。在体外,异别孕烯醇酮、UC1011、GR3027和17PA可拮抗别孕烯醇酮/THDOC增强的GABA介导的GABAA受体活性,而GABA本身的作用不受影响。