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作 者:方虹[1] 郭庆林[1] 张贵祥[1] 赵海涛[1] 俞高龙[1] 赵喜平[1] 葛雅丽[1]
机构地区:[1]第四军医大学附属西京医院放射科
出 处:《中华放射学杂志》1997年第1期35-39,共5页Chinese Journal of Radiology
摘 要:目的:应用1H磁共振波谱技术研究正常人脑内化合物的含量和分布。材料和方法:应用1.5T磁共振仪对18例正常人脑进行1H波谱测试,测量的感兴趣区包括大脑皮层、白质、丘脑和小脑,所用序列为激励回波探测序列(stimulatedechoaquisitionmode,STEAM)。结果:1H磁共振波谱可以检测出脑内许多化合物,如N-乙酰门冬氨酸(NAA)、含胆碱类化合物(Cho)、肌酸和磷酸肌酸(Cr+Pcr)、谷氨酸和谷氨酰胺(Glu+Gln)、脂质、乳酸等。各化合物的浓度在脑的不同区域存在着差异。NAA/Cho比值在灰质最高,小脑最低。Cr/Cho比值在小脑最高、白质最低。设定肌酸的浓度在灰质和小脑为10mmol/L,在白质和丘脑为11mmol/L,计算NAA的绝对浓度为13~23mmol/L,并且灰质的含量高于小脑和丘脑。结论:1H磁共振波谱技术可无创性检测出脑组织中与能量代谢、氨基酸、脂肪酸及神经递质有关的化合物,并可定量测定,有助于研究生理和疾病时脑生化改变。Purpose: To study the 1 H MR spectrum of normal human brain and the concentration and distribution of main metabolites using 1 H MR spectroscopy. Materials and methods: Eighteen health human brains were examined by conventional 1.5T MRI system. Volume of interest (VOI) included temporal lobe (mainly gray matter), thalamus, cerebellum as well as white matter. Results: Proton MR spectroscopy can detect a variety of metabolites in human brain in vivo. The main detectable metabolites were N acetyl aspartate (NAA: at 2.02ppm), cholinecontaining compounds (Cho: at 3.2ppm), phosphocreatine and creatine (PCr+Cr: at 3.0ppm), glutamine and glutamate (Gln+Glu: at 2.34-2.45ppm), lipids (Lip: at 1.0ppm) and lactate (Lac: at 1.3ppm). The metabolite concentration varied in different parts of the brain. The relative signal intensity calculation showed that: NAA/Cho ratio is the highest in gray matter and lowest in cerebellun. Cr/Cho is the highest in cerebellum and lowest in white matter. The assumed creatine concentration is 10mmol/L for gray matter and cerebellum, 11 mmol/L for white matter and thalamus, the absolute concentration of NAA in the brain is about 13-23 mmol/L, and is higher in gray matter than in cerebellum and thalamus. Conclusion: Proton MR spectroscopy is a new noninvasive method which can be used to detect a number of chemical compounds pertaining to energy metabolism, free amino acids, fatty acids and neurotransmitters in the brain. It is useful to assess the cerebral biochemical changes in vivo both in healthy subjects and in patients with various brain disease.
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