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논문 기본 정보

자료유형
학술저널
저자정보
Hu, Zhenzhen (College of Pharmacy, Chungbuk National University) Park, Kwang-Soon (College of Pharmacy, Chungbuk National University) Han, Jin-Yi (Research Institute of Veterinary Medicine, Chungbuk National University) Jang, Choon-Gon (School of Pharmacy, Sungkyunkwan University) Oh, Sei-Kwan (College of Medicine, Ewha Womans University) Kim, Hyoung-Chun (College of Pharmacy, Kangwon National University) Yang, Chae-Ha (College of Oriental Medicine, Daegu Haany University) Kim, Eun-Jeong (Korea Food and Drug Administration) Oh, Ki-Wan (College of Pharmacy, Chungbuk National University)
저널정보
한국응용약물학회 Biomolecules & Therapeutics(구 응용약물학회지) Biomolecules & therapeutics 제19권 제1호
발행연도
2011.1
수록면
45 - 51 (7page)

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These experiments were designed to use typical makers from behaviors and molecular basis in addicted animals of morphine and cocaine. Morphine has been widely abused with a high physical dependence liability. Morphine withdrawal activates the intracellular cAMP signaling pathway and further leads to changes in the expression of the cAMP response element binding protein (CREB), which may be important to the development and expression of morphine dependence. From these experiments, repeated morphine (10 mg/kg, twice per day for 7 days) developed physical dependence. Withdrawal signs were precipitated by naloxone and also increased the expression of the CREB. In addition, repeated exposure of cocaine (15 mg/kg) to mice develops locomotor sensitization and produced lasting behavioral sensitivity. Cocaine- and amphetamine-regulated transcript peptide (CART) peptide was up-regulated by repeated administration of cocaine in the striatum. Therefore, repeated morphine induced the development of physical dependence and increased pCREB. In addition, repeated cocaine induced locomotor sensitization and over-expressed CART peptide. In conclusion, the development of physical dependence and pCREB for morphine, and locomotor sensitization and CART peptide over-expression for cocaine would be useful markers to predict the abuse potential of opioid analgesics and pychostimulant drugs in animals, respectively.

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