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    題名: 愷他命和右旋愷他命異構物對大鼠行為及神經化學的影響效果:與右旋安非他命相比較
    Behavioral and Neurochemical Effects of RS-ketamine and S-ketamine in Rats: Compared with d-Amphetamine
    作者: 王傳堯
    Wang, Chuan-Yao
    貢獻者: 廖瑞銘
    趙知章

    Liao, Ruey-Ming
    Chao, Chih-Chang

    王傳堯
    Wang, Chuan-Yao
    關鍵詞: 藥物酬賞和成癮
    制約性場地偏好
    行為致敏化
    麩胺酸NMDA受體
    多巴胺
    大鼠
    Drug reward and addiction
    Conditioned place preference
    Behavioral sensitization
    Glutamate NMDA receptor
    Dopamine
    Rat
    日期: 2022
    上傳時間: 2022-08-01 18:14:28 (UTC+8)
    摘要: 愷他命是一種非競爭性氮-甲基天門冬胺酸(N-methyl-D-aspartate)受體拮抗劑,近年來被用於治療憂鬱症,但其神經行為機制仍然有待確證,其中一項問題是有關愷他命會致使精神迷幻和藥物上癮的效果。本研究實驗一利用一種同時測量制約性場地偏好和行為致敏化的藥癮行為動物模式,針對利用消旋性愷他命 (RS-KET)、右旋性愷他命異構物 [S(+)-KET]、和安非他命 (d-AMP),測試其藥物酬賞的行為藥理作用;實驗二以西方墨點法檢測五個腦區之麩胺酸與多巴胺相關的蛋白質、及大腦衍生神經滋養因子之表現量,分析藥物作用的神經化學機制。實驗一藉由七次間歇重複注射藥物的操弄,結果發現d-AMP組顯著引發場地偏好及行為致敏化的效果;RS-KET組及S-KET組沒有引發顯著的場地制約偏好,但有行為致敏化的反應,惟其藥效較d-AMP組弱。實驗二生化分析的結果顯示藥物影響效果包含:(1)依核和背側紋狀體之NMDA受體 (GluN1、GluN2A和GluN2B)蛋白質表現量顯著減少,(2)多巴胺相關蛋白質(D1受體、D2受體、和DAT)表現量依據腦區和藥物的不同而有差異,(3)BDNF的蛋白質表現量僅在杏仁核有增加的效應。綜合而言,相對於d-AMP引發制約性場地偏好及行為致敏化的行為藥理效果,RS-KET及S-KET的效果比較不明顯。這三種藥物之間的行為藥理差異,與不同腦區的特定蛋白質表現量變化有關。本研究顯示愷他命的藥物酬賞性質有別於心理興奮劑,這兩類藥物影響麩胺酸與多巴胺傳遞系統相關的蛋白質表現有差異,此結果可供後續探討這兩類藥物調控成癮行為的神經生物機制之用。
    Ketamine is a non-competitive N-methyl-D-aspartate receptor antagonist that has recently been repurposed in depression therapy, although the underlying neurobehavioral mechanisms remain elusive. One of the key issues should be concerned is that ketamine may cause psychotic and addictive effects in its users. Thus, this study, in Experiment 1, was designed to investigate the effects of racemic ketamine [RS (+/-)-ketamine; RS-KET] and it S-isomer [S (+)-ketamine; S-KET] respectively, on a behavioral protocol combining tests of conditioned place preference (CPP) and behavioral sensitization (BS). Additionally, d-amphetamine (d-AMP) treatment was conducted as a positive control. In the Experiment 2, after completing behavioral test, the expression levels of NMDA receptor subunits, dopamine-related proteins, and brain-derived neurotrophic factor (BDNF) were analyzed by western blotting. The results of Experiment 1 showed that the d-AMP group significantly displayed CPP and BS effects following a drug treatment of 7-time intermittent repeated injections, while the RS-KET and S-KET groups did not have CPP but showed various degrees of BS. However, the magnitude of BS induced by RS-KET or S-KET was smaller than that of d-AMP. The results of Experiment 2 revealed drug effects significantly measured on (1) decreases of the protein expressions of NMDA receptor subunits (GluN1, GluN2A, and GluN2B) in both the nucleus accumbens and dorsal striatum, (2) region-dependent changes in dopamine-related proteins (D1 receptor, D2 receptor, and DAT), and (3) no change of BDNF except detecting an increase in the amygdala. Together, RS-KET and S-KET did not produce the effects of CPP and BS as profound as d-AMP on the present behavioral task. The disparity between drug treatments is related to the change of certain protein expression on specific brain area. These results indicate the differential characteristics of drug reward between ketamine and psychostimulant which could be associated with different patterns of protein expressions involved in the glutamate and dopamine transmission systems, highlighting the neurobiological mechanisms of drug reward and addiction underlying these drugs to be unfolded in future study.
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    描述: 碩士
    國立政治大學
    神經科學研究所
    108754003
    資料來源: http://thesis.lib.nccu.edu.tw/record/#G0108754003
    資料類型: thesis
    DOI: 10.6814/NCCU202200873
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