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

机译:氯胺酮调节雄性大鼠脑和外周组织中的TRH和TRH样肽转换

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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 mu l of sterile saline containing either 0 or 5 mg/ml Glu-TRH. One, 2 or 4 h later, the brain levels of TRH and TRH-like peptides were measured in various brain regions and peripheral tissues. At 1 h 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 (up arrow) and/or decreases (down arrow), were: hypothalamus (9 up arrow); piriform cortex (8 up arrow); entorhinal cortex (7 up arrow); nucleus accumbens (7 up arrow); posterior cingulate (5 up arrow); striatum (4 up arrow); frontal cortex (2 up arrow,3 down arrow); amygdala (3 up arrow); medulla oblongata (1 up arrow,2 down arrow); cerebellum (2 up arrow); hippocampus (2 up arrow); anterior cingulate (2 up arrow). The corresponding changes in peripheral tissues were: adrenals (8 up arrow); epididymis (4 up arrow); testis (1 up arrow,3 down arrow); pancreas (1 up arrow); prostate (1 up arrow). We conclude that TRH and TRH-like peptides may be downstream mediators of the rapid antidepressant actions of ketamine. Published by Elsevier Inc.
机译:重度抑郁症是最大的单一医疗保健负担,其起病缓慢且疗效通常有限。氯胺酮是一种广泛用作儿科和兽用麻醉剂的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。对氯胺酮的神经生化机制有更全面的了解,应该可以找到更安全的替代方法。氯胺酮的某些生理和药理作用与TRH(pGlu-His-Pro-NH2)和TRH样肽(pGlu-X-Pro-NH2)的合成和释放增加一致,其中“ X”可以是任何氨基酸残基。而且,TRH样肽本身是用于治疗重度抑郁症,焦虑症,躁郁症,癫痫症,阿尔茨海默氏病和帕金森氏病的潜在治疗剂。由于这些原因,雄性Sprague-Dawley大鼠用162 mg / kg ip氯胺酮麻醉,然后鼻腔内注入20μl含0或5 mg / ml Glu-TRH的无菌盐水。 1、2或4小时后,在各种大脑区域和周围组织中测量了TRH和TRH样肽的脑水平。仅在氯胺酮后1小时的大脑中,TRH和TRH样肽的水平在52种情况下显着增加(由于生物合成增加和/或释放降低),在5种情况下下降。这些变化按脑区的顺序排列,依次为显着增加(向上箭头)和/或减少(向下箭头),分别是:下丘脑(9个向上箭头);下丘脑(9个向上箭头);下丘脑(9个向上箭头)。梨状皮层(8向上箭头);内嗅皮层(7向上箭头);伏伏核(7向上箭头);后扣带(5向上箭头);纹状体(4向上箭头);额叶皮层(2向上箭头,3向下箭头);杏仁核(3向上箭头);延髓(1向上箭头,2向下箭头);小脑(2向上箭头);海马(2向上箭头);前扣带回(2向上箭头)。周围组织的相应变化是:肾上腺(8向上箭头);附睾(4向上箭头);睾丸(1个向上箭头,3个向下箭头);胰腺(1向上箭头);前列腺(向上箭头1个)。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。由Elsevier Inc.发布

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