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氯胺酮可调节雄性大鼠脑和外周组织中促甲状腺激素释放激素(TRH)及TRH样肽的更新。

Ketamine modulates TRH and TRH-like peptide turnover in brain and peripheral tissues of male rats.

作者信息

Pekary A Eugene, Sattin Albert, Lloyd Robert L

机构信息

Research Services, VA Greater Los Angeles Healthcare System, University of California, Los Angeles, CA 90073, United States; Center for Ulcer Research and Education, VA Greater Los Angeles Healthcare System, University of California, Los Angeles, CA 90073, United States; Department of Medicine, University of California, Los Angeles, CA 90073, United States.

Research Services, VA Greater Los Angeles Healthcare System, University of California, Los Angeles, CA 90073, United States; Psychiatry Services, VA Greater Los Angeles Healthcare System, University of California, Los Angeles, CA 90073, United States; Departments of Psychiatry & Biobehavioral Sciences, University of California, Los Angeles, CA 90073, United States; Brain Research Institute, University of California, Los Angeles, CA 90073, United States.

出版信息

Peptides. 2015 Jul;69:66-76. doi: 10.1016/j.peptides.2015.04.003. Epub 2015 Apr 13.

Abstract

Major depression is the largest single healthcare burden with treatments of slow onset and often limited efficacy. Ketamine, a NMDA antagonist used extensively as a pediatric and veterinary anesthetic, has recently been shown to be a rapid acting antidepressant, making it a potential lifesaver for suicidal patients. Side effects and risk of abuse limit the chronic use of ketamine. More complete understanding of the neurobiochemical mechanisms of ketamine should lead to safer alternatives. Some of the physiological and pharmacological actions of ketamine are consistent with increased synthesis and release of TRH (pGlu-His-Pro-NH2), and TRH-like peptides (pGlu-X-Pro-NH2) where "X" can be any amino acid residue. Moreover, TRH-like peptides are themselves potential therapeutic agents for the treatment of major depression, anxiety, bipolar disorder, epilepsy, Alzheimer's and Parkinson's diseases. For these reasons, male Sprague-Dawley rats were anesthetized with 162 mg/kg ip ketamine and then infused intranasally with 20 μl of sterile saline containing either 0 or 5 mg/ml Glu-TRH. One, 2 or 4h later, the brain levels of TRH and TRH-like peptides were measured in various brain regions and peripheral tissues. At 1h in brain following ketamine only, the levels of TRH and TRH-like peptides were significantly increased in 52 instances (due to increased biosynthesis and/or decreased release) or decreased in five instances. These changes, listed by brain region in order of decreasing number of significant increases (↑) and/or decreases (↓), were: hypothalamus (9↑); piriform cortex (8↑); entorhinal cortex (7↑); nucleus accumbens (7↑); posterior cingulate (5↑); striatum (4↑); frontal cortex (2↑,3↓); amygdala (3↑); medulla oblongata (1↑,2↓); cerebellum (2↑); hippocampus (2↑); anterior cingulate (2↑). The corresponding changes in peripheral tissues were: adrenals (8↑); epididymis (4↑); testis (1↑,3↓); pancreas (1↑); prostate (1↑). We conclude that TRH and TRH-like peptides may be downstream mediators of the rapid antidepressant actions of ketamine.

摘要

重度抑郁症是最大的单一医疗负担,其治疗起效缓慢且疗效往往有限。氯胺酮是一种广泛用作儿科和兽医麻醉剂的N-甲基-D-天冬氨酸(NMDA)拮抗剂,最近已被证明是一种速效抗抑郁药,使其成为自杀患者的潜在救星。副作用和滥用风险限制了氯胺酮的长期使用。对氯胺酮神经生化机制的更全面了解应能带来更安全的替代药物。氯胺酮的一些生理和药理作用与促甲状腺激素释放激素(TRH,pGlu-His-Pro-NH2)以及TRH样肽(pGlu-X-Pro-NH2,其中“X”可以是任何氨基酸残基)的合成和释放增加一致。此外,TRH样肽本身就是治疗重度抑郁症、焦虑症、双相情感障碍、癫痫、阿尔茨海默病和帕金森病的潜在治疗药物。基于这些原因,将雄性Sprague-Dawley大鼠用162mg/kg腹腔注射氯胺酮麻醉,然后经鼻内注入20μl含有0或5mg/ml Glu-TRH的无菌生理盐水。1、2或4小时后,在各个脑区和外周组织中测量TRH和TRH样肽的脑内水平。仅在给予氯胺酮后1小时,TRH和TRH样肽的水平在52例中显著升高(由于生物合成增加和/或释放减少),在5例中降低。这些变化按脑区列出,按显著升高(↑)和/或降低(↓)数量递减的顺序为:下丘脑(9↑);梨状皮质(8↑);内嗅皮质(7↑);伏隔核(7↑);后扣带回(5↑);纹状体(4↑);额叶皮质(2↑,3↓);杏仁核(3↑);延髓(1↑,2↓);小脑(2↑);海马体(2↑);前扣带回(2↑)。外周组织中的相应变化为:肾上腺(8↑);附睾(4↑);睾丸(1↑,3↓);胰腺(1↑);前列腺(1↑)。我们得出结论,TRH和TRH样肽可能是氯胺酮快速抗抑郁作用的下游介质。

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