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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

漢畫中闕形圖像及其文化意涵研究 / The research on watchtower's image in HAN danasty stone relief and it's culture meanings

鄒旻樺, Tsou, Ming Hua Unknown Date (has links)
在研究中國古代世界時,除了關注書面文獻的敘事外,還必須留意非訴諸文字的書寫,其中漢代畫像就以圖像形式,敘說著漢人的民風民俗、思維模式以及生死觀念,這是研究漢代不可忽略的重要材料。在中國各個畫像石出土地區,我們不約而同發現了「闕形」圖像,在現實世界中,闕是漢代非常重要的建築樣式,從聚落、宮殿到祠廟、坟墓都有闕建築的身影,它一方面作為入口標誌,另一方面又起著區隔內外的作用,更與當時社會、政治、經濟狀況密切相關。在墓葬世界中,闕形圖像無論於墓葬空間中的配置位置,或與其他畫像題材的配對,均呈現穩定的邏輯套式,這說明了闕形圖像在漢人的生死觀念中,就如同語言文字或宗教儀軌具,是一種有力量的符號、象徵。因此本研究將嘗試在歷來學者的研究基礎上,綜合建築學、人類學、宗教學的研究成果,從實體闕建築以及漢畫中闕形圖像進行類型分析,以澄清闕形圖像對闕建築的承繼與超越,進而探究闕形圖像所表達漢人精神世界的多重文化意涵。
2

探討N-甲基-D-天門冬胺酸受體在時距相關的操作式制約行為與空間工作記憶的角色:memantine的神經心理藥理學機制 / Investigation of the role of N-methyl-D-aspartate (NMDA) receptors on temporal operant behavior and spatial working memory: the underlying neuropsychopharmacological mechanisms of memantine

陳碩甫 Unknown Date (has links)
認知功能的提升是當今神經科學領域中的研究重點之一,但其神經機制尚有待釐清。本研究利用一種用於改善阿茲海默症臨床的非競爭型N-甲基-D-天門冬胺酸受體拮抗劑memantine,檢測其對於大白鼠在不同時距相關操作式制約行為及空間工作記憶行為之影響效果。實驗一為針對時間屬性的操作式制約行為實驗,運用大白鼠的區辯性增強低頻反應作業(DRL 10秒行為)與固定時距作業(FI 30秒行為)之行為作業,並操弄連續訓練與間歇訓練的兩種不同模式,測試memantine對前述四組受試的操作式制約行為在表現、消除與自發恢復等三階段之劑量反應。實驗二利用配對性延遲T迷津作業區分出不等基準線(表現好與表現差)之受試,再加以藥理實驗,測試memantine對於前述兩組受試之劑量反應。實驗一結果顯示,受試在兩種不同訓練模式下經十五次習得訓練後,在兩種操作式壓桿行為的壓桿反應相關指標中都有明顯的差異,這證實不同的行為訓練模式會導致學習後的表現有差異之別。memantine藥理實驗結果顯示,此藥對於上述四組受試的操作式行為之三階段的影響效果,會因為不同訓練模式與不同作業而異。實驗二結果顯示,memantine提高空間工作記憶的正確率在表現不好的組別有很顯著的藥效,這證實memantine對於空間式工作記憶行為的影響,也會因學習基準線的不同水平而異。在行為實驗後所進行的蛋白質表現量檢測中,memantine(5 mg/kg)只對五個測試腦區中的背側紋狀體中ERK1磷酸化程度有明顯上升的影響,而其對ERK2及CREB的磷酸化在所有腦組織中皆沒有顯著的影響。綜合以上結果,memantine影響時間與空間屬性的相關行為之藥理效果,會依行為的不同習得歷程(或行為背景經驗)及基準線表現程度而異,而此項行為藥理效果,可能與紋狀體中ERK1的磷酸化有關。 / The neural basis of cognitive enhancement is one of the intriguing topics in neuroscience research; however, the underlying neural mechanisms remain to be elucidated. This study examined the effects of memantine, a non-competitive N-methyl-D-aspartate (NMDA) receptor antagonist which is used to treat Alzheimer’s disease in clinic, on operant behaviors and spatial working memory. In Experiment 1, using the differential reinforcement for low-rate-response 10 sec (DRL 10s) and the fixed-interval 30 sec (FI 30s) operant tasks, and with the manipulation of two different training regimens (continuous vs. intermittent) in the acquisition phase, the effects of memantine were evaluated in three stages of behavioral tests including the performance (right after the end of 15-day acquisition), the extinction, and the spontaneous recovery (after the extinction). In Experiment 2, memantine were tested in the subjects with different level of baseline performance (good vs. bad) on the distinctive patterns of operant responding in four different groups which received DRL 10s and FI 30s with different training regimens; indicating that behavioral task and training background are critical to the operant performance of temporal operant behaviors. Such behavioral outcomes led the dissociable effects of memantine appeared in between the four groups as tested in all three different stages. The results of Experiment 2 showed a profound improvement of the correct responses rate on spatial working memory in the low-baseline group as compared to the higher-baseline group. With a pretreatment of memantine (5 mg/kg), brain tissues in five selected areas were collected for western blot assays of ERK 1, ERK 2, and CREB. The results only revealed a significant increase of ERK 1 phosphorylation in the dorsal striatum. Together, the effects of memantine to improve cognition-associated processes in the temporal operant behaviors and the baseline of performance, and the present observation of cognition-enhancing effects of memantine may be resulted by the ERK 1 phosphorylation in the dorsal striatum.

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