The role of adenosine receptor in neurotoxicity induced by caffeine exposure during synaptogenesis

碩士 === 慈濟大學 === 藥理暨毒理學研究所 === 93 === Caffeine is used clinically to treat apnea in preterm infants. The brain developmental stage of preterm infants is usually at a period of rapid brain growth, referred as synaptogenesis, which occurs during early postnatal life in rats. In this period, the central...

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Main Authors: Hong-Zhen Pan, 潘虹蓁
Other Authors: Hwei-Hsien Chen
Format: Others
Language:en_US
Published: 2005
Online Access:http://ndltd.ncl.edu.tw/handle/80109066264190562265
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spelling ndltd-TW-093TCU052290112015-10-13T15:01:30Z http://ndltd.ncl.edu.tw/handle/80109066264190562265 The role of adenosine receptor in neurotoxicity induced by caffeine exposure during synaptogenesis 突觸形成期暴露咖啡因引起之神經毒性:腺苷酸受體扮演的角色 Hong-Zhen Pan 潘虹蓁 碩士 慈濟大學 藥理暨毒理學研究所 93 Caffeine is used clinically to treat apnea in preterm infants. The brain developmental stage of preterm infants is usually at a period of rapid brain growth, referred as synaptogenesis, which occurs during early postnatal life in rats. In this period, the central nerve system (CNS) is highly sensitive to CNS acting drugs. In this study, we evaluated whether caffeine treatment during synaptogenesis produces any developmental and behavioral impairment. Since caffeine is an antagonist of the adenosine A1and A2A receptors, the adenosine receptor-related behaviors, such as analgesia (hot plate and tail flick test), anti-anxiety (elevated plus maze and dark-light transition test), learning and memory (step-through passive avoidance test and Morris water maze), hypothermia (rectal temperature) and hypolocomotion (locomotor activity) were examined. Sprague-Dawley rats administered either deionized water or caffeine (15-20 mg/kg/day) through gavage (0.05 ml/10 g) over postnatal days (PN) 2-6. The response latency in caffeine-exposed rats was significantly reduced in hot plate test but not in tail flick test. Caffeine-exposed rats showed less anxiety than control in the elevated plus maze and dark-light transition. In learning and memory test, caffeine-exposed rats showed impairment of memory retention in step through avoidance learning test but no differences in spatial learning ability in Morris water maze. Moreover, neonatal caffeine exposure increased adenosine receptor agonist-induced reduction in locomotion and rectal temperature compared with control rats. RT-PCR analysis demonstrated that adenosine receptor A2A subunit in the striatum of female rats was increased. However, western blot analysis showed the levels of adenosine A1 and A2a receptor was unaffected except A1 receptor expression increased in amygdala. These results indicate that neonatal caffeine exposure alters the adenosine receptor-related behaviors and the sensitivity to adenosine agonists, suggesting the risk may exist in preterm newborns treated for apnea with caffeine. Hwei-Hsien Chen 陳慧諴 2005 學位論文 ; thesis 69 en_US
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description 碩士 === 慈濟大學 === 藥理暨毒理學研究所 === 93 === Caffeine is used clinically to treat apnea in preterm infants. The brain developmental stage of preterm infants is usually at a period of rapid brain growth, referred as synaptogenesis, which occurs during early postnatal life in rats. In this period, the central nerve system (CNS) is highly sensitive to CNS acting drugs. In this study, we evaluated whether caffeine treatment during synaptogenesis produces any developmental and behavioral impairment. Since caffeine is an antagonist of the adenosine A1and A2A receptors, the adenosine receptor-related behaviors, such as analgesia (hot plate and tail flick test), anti-anxiety (elevated plus maze and dark-light transition test), learning and memory (step-through passive avoidance test and Morris water maze), hypothermia (rectal temperature) and hypolocomotion (locomotor activity) were examined. Sprague-Dawley rats administered either deionized water or caffeine (15-20 mg/kg/day) through gavage (0.05 ml/10 g) over postnatal days (PN) 2-6. The response latency in caffeine-exposed rats was significantly reduced in hot plate test but not in tail flick test. Caffeine-exposed rats showed less anxiety than control in the elevated plus maze and dark-light transition. In learning and memory test, caffeine-exposed rats showed impairment of memory retention in step through avoidance learning test but no differences in spatial learning ability in Morris water maze. Moreover, neonatal caffeine exposure increased adenosine receptor agonist-induced reduction in locomotion and rectal temperature compared with control rats. RT-PCR analysis demonstrated that adenosine receptor A2A subunit in the striatum of female rats was increased. However, western blot analysis showed the levels of adenosine A1 and A2a receptor was unaffected except A1 receptor expression increased in amygdala. These results indicate that neonatal caffeine exposure alters the adenosine receptor-related behaviors and the sensitivity to adenosine agonists, suggesting the risk may exist in preterm newborns treated for apnea with caffeine.
author2 Hwei-Hsien Chen
author_facet Hwei-Hsien Chen
Hong-Zhen Pan
潘虹蓁
author Hong-Zhen Pan
潘虹蓁
spellingShingle Hong-Zhen Pan
潘虹蓁
The role of adenosine receptor in neurotoxicity induced by caffeine exposure during synaptogenesis
author_sort Hong-Zhen Pan
title The role of adenosine receptor in neurotoxicity induced by caffeine exposure during synaptogenesis
title_short The role of adenosine receptor in neurotoxicity induced by caffeine exposure during synaptogenesis
title_full The role of adenosine receptor in neurotoxicity induced by caffeine exposure during synaptogenesis
title_fullStr The role of adenosine receptor in neurotoxicity induced by caffeine exposure during synaptogenesis
title_full_unstemmed The role of adenosine receptor in neurotoxicity induced by caffeine exposure during synaptogenesis
title_sort role of adenosine receptor in neurotoxicity induced by caffeine exposure during synaptogenesis
publishDate 2005
url http://ndltd.ncl.edu.tw/handle/80109066264190562265
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