Effect of α-chloralose dosage on anesthesia depth, cortical evoked potential and fMRI in the rat.

碩士 === 國立臺灣大學 === 動物學研究研究所 === 93 === Functional magnetic resonance imaging (fMRI) is an important tool for exploring brain activities. A stable anesthetized animal preparation is critically important for fMRI applications. The present study intended to determine the optimal infusion rate of α-chlor...

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Main Authors: Wei-Fan Chen, 陳韋凡
Other Authors: 嚴震東
Format: Others
Language:en_US
Published: 2005
Online Access:http://ndltd.ncl.edu.tw/handle/05071248255614863095
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spelling ndltd-TW-093NTU053120102015-12-21T04:04:13Z http://ndltd.ncl.edu.tw/handle/05071248255614863095 Effect of α-chloralose dosage on anesthesia depth, cortical evoked potential and fMRI in the rat. α-氯醛醣麻醉劑量對功能性磁振造影相關參數之影響 Wei-Fan Chen 陳韋凡 碩士 國立臺灣大學 動物學研究研究所 93 Functional magnetic resonance imaging (fMRI) is an important tool for exploring brain activities. A stable anesthetized animal preparation is critically important for fMRI applications. The present study intended to determine the optimal infusion rate of α-chloralose anesthesia, the most popular anesthetics used in animal fMRI. In addition, the analgesia effect of morphine was tested by giving morphine before electrical stimulation. Long-Evans female rats (220 ~ 320 g) were used. After halothane induction, α-chloralose was given in an intravenous bolus injection (80 mg/kg). Subsequently, 3 different maintenance dosages were compared. These were administrated through intravenous infusion:high (60 mg/kg/hr), low (30 mg/kg/hr) or vehicle. During the 5 hours of recording period, blood pressure, heart rate, O2 and CO2 concentration in arterial blood were monitored. In addition, somatosensory evoked potentials (EEG) and flexor reflex activities (EMG) after hind paw electrical stimulation (2 mA, 0.5 ms, 0.3 Hz) were recorded every half hour. Under suitable infusion rate (30 mg/kg/hr), the physiological conditions remained stable for 5 hr, while the results suggested that the high dose and vehicle were not appropriate dosages for a stable anesthesia. Also, fMRI activations of the contralateral primary somatosensory cortex (SI) were readily observed under low dosage of α-chloralose infusion. In the morphine effect study, activations of anterior cingulate cortex (ACC), motor area/cingulate cortex (CC) and SI were attenuated after morphine administration. However, BOLD signals of SI were recovered after 3 hours, while the responses in ACC, motor area/CC remained suppressed. This study demonstrates that a steady α-chloralose anesthesia can be achieved for fMRI study, which can be utilized in the study of drug, lesion or other brain experiments. 嚴震東 2005 學位論文 ; thesis 50 en_US
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description 碩士 === 國立臺灣大學 === 動物學研究研究所 === 93 === Functional magnetic resonance imaging (fMRI) is an important tool for exploring brain activities. A stable anesthetized animal preparation is critically important for fMRI applications. The present study intended to determine the optimal infusion rate of α-chloralose anesthesia, the most popular anesthetics used in animal fMRI. In addition, the analgesia effect of morphine was tested by giving morphine before electrical stimulation. Long-Evans female rats (220 ~ 320 g) were used. After halothane induction, α-chloralose was given in an intravenous bolus injection (80 mg/kg). Subsequently, 3 different maintenance dosages were compared. These were administrated through intravenous infusion:high (60 mg/kg/hr), low (30 mg/kg/hr) or vehicle. During the 5 hours of recording period, blood pressure, heart rate, O2 and CO2 concentration in arterial blood were monitored. In addition, somatosensory evoked potentials (EEG) and flexor reflex activities (EMG) after hind paw electrical stimulation (2 mA, 0.5 ms, 0.3 Hz) were recorded every half hour. Under suitable infusion rate (30 mg/kg/hr), the physiological conditions remained stable for 5 hr, while the results suggested that the high dose and vehicle were not appropriate dosages for a stable anesthesia. Also, fMRI activations of the contralateral primary somatosensory cortex (SI) were readily observed under low dosage of α-chloralose infusion. In the morphine effect study, activations of anterior cingulate cortex (ACC), motor area/cingulate cortex (CC) and SI were attenuated after morphine administration. However, BOLD signals of SI were recovered after 3 hours, while the responses in ACC, motor area/CC remained suppressed. This study demonstrates that a steady α-chloralose anesthesia can be achieved for fMRI study, which can be utilized in the study of drug, lesion or other brain experiments.
author2 嚴震東
author_facet 嚴震東
Wei-Fan Chen
陳韋凡
author Wei-Fan Chen
陳韋凡
spellingShingle Wei-Fan Chen
陳韋凡
Effect of α-chloralose dosage on anesthesia depth, cortical evoked potential and fMRI in the rat.
author_sort Wei-Fan Chen
title Effect of α-chloralose dosage on anesthesia depth, cortical evoked potential and fMRI in the rat.
title_short Effect of α-chloralose dosage on anesthesia depth, cortical evoked potential and fMRI in the rat.
title_full Effect of α-chloralose dosage on anesthesia depth, cortical evoked potential and fMRI in the rat.
title_fullStr Effect of α-chloralose dosage on anesthesia depth, cortical evoked potential and fMRI in the rat.
title_full_unstemmed Effect of α-chloralose dosage on anesthesia depth, cortical evoked potential and fMRI in the rat.
title_sort effect of α-chloralose dosage on anesthesia depth, cortical evoked potential and fmri in the rat.
publishDate 2005
url http://ndltd.ncl.edu.tw/handle/05071248255614863095
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