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67Ga在正常器官中的滞留及亚细胞分布

Retention and subcellular distribution of 67Ga in normal organs.

作者信息

Ando A, Ando I, Hiraki T, Hisada K, Nitta K, Ogawa H

出版信息

Nuklearmedizin. 1986 Apr;25(2):45-9.

PMID:3714511
Abstract

Using normal rats, retention values and subcellular distribution of 67Ga in each organ were investigated. At 10 min after administration of 67Ga-citrate the retention value of 67Ga in blood was 6.77% dose/g, and this value decreased with time. The values for skeletal muscle, lung, pancreas, adrenal, heart muscle, brain, small intestine, large intestine and spinal cord were the highest at 10 min after administration, and they decreased with time. Conversely, this value in bone increased until 10 days after injection. But in the liver, kidney, and stomach, these values increased with time after administration and were highest 24 h or 48 h after injection. After that, they decreased with time. The value in spleen reached a plateau 48 h after administration, and hardly varied for 10 days. From the results of subcellular fractionation, it was deduced that lysosome plays quite an important role in the concentration of 67Ga in small intestine, stomach, lung, kidney and pancreas; a lesser role in its concentration in heart muscle, and hardly any role in the 67Ga accumulation in skeletal muscle. In spleen, the contents in nuclear, mitochondrial, microsomal, and supernatant fractions all contributed to the accumulation of 67Ga.

摘要

使用正常大鼠,研究了67Ga在各器官中的滞留值和亚细胞分布。给予柠檬酸镓67Ga后10分钟,血液中67Ga的滞留值为6.77%剂量/克,该值随时间下降。骨骼肌、肺、胰腺、肾上腺、心肌、脑、小肠、大肠和脊髓的值在给药后10分钟时最高,随后随时间下降。相反,骨中的该值在注射后10天内持续升高。但在肝脏、肾脏和胃中,这些值在给药后随时间升高,在注射后24小时或48小时时达到最高,之后随时间下降。脾脏中的值在给药后48小时达到平台期,10天内几乎没有变化。从亚细胞分级分离的结果推断,溶酶体在小肠、胃、肺、肾脏和胰腺中67Ga的浓集中起相当重要的作用;在心肌浓集中起的作用较小,在骨骼肌中67Ga的积累中几乎不起作用。在脾脏中,核、线粒体、微粒体和上清液组分中的含量均对67Ga的积累有贡献。

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