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转铁蛋白、胰岛素和孕酮可调节未分化的PC12细胞中甲羟戊酸途径产物辅酶Q和胆固醇的细胞内浓度。

Transferrin, insulin, and progesterone modulate intracellular concentrations of coenzyme Q and cholesterol, products of the mevalonate pathway, in undifferentiated PC12 cells.

作者信息

Nakamura Akari, Aida Yukina, Okamoto Mizuho, Maeda Ayaka, Nagao Ayaka, Kitatani Kanae, Takekoshi Susumu, Fujisawa Akio, Yamamoto Yorihiro, Kashiba Misato

机构信息

School of Bionics, Tokyo University of Technology, 1404-1 Katakura-machi, Hachioji, Tokyo 192-0982, Japan.

School of Medicine, Tokai University, 143 Shimokasuya, Isehara, Kanagawa 259-1193, Japan.

出版信息

J Clin Biochem Nutr. 2023 May;72(3):199-206. doi: 10.3164/jcbn.22-115. Epub 2023 Mar 18.

Abstract

Coenzyme Q (CoQ) is important not only as an essential lipid for the mitochondrial electron transport system, but also as an antioxidant. CoQ levels decrease during aging and in various diseases. Orally administered CoQ is not readily taken up in the brain, so it is necessary to develop a method to increase the amount of CoQ in neurons. CoQ is synthesized via mevalonate pathway, like cholesterol. Transferrin, insulin, and progesterone are factors used in the culture of neurons. In this study, we determined the effect of these reagents on cellular CoQ and cholesterol levels. The administration of transferrin, insulin, and progesterone increased cellular CoQ levels in undifferentiated PC12 cells. When serum was removed and only insulin was administered, intracellular CoQ levels increased. This increase was even more pronounced with concurrent administration of transferrin, insulin, and progesterone. Cholesterol level decreased by the administration of transferrin, insulin, and progesterone. Progesterone treatment lowered intracellular cholesterol levels in a concentration-dependent manner. Our findings suggest that transferrin, insulin, and progesterone may be useful in regulating CoQ levels and cholesterol levels, which are products of the mevalonate pathway.

摘要

辅酶Q(CoQ)不仅作为线粒体电子传递系统的必需脂质很重要,而且作为一种抗氧化剂也很重要。辅酶Q水平在衰老过程中和各种疾病中会降低。口服辅酶Q不易被大脑吸收,因此有必要开发一种增加神经元中辅酶Q含量的方法。辅酶Q像胆固醇一样通过甲羟戊酸途径合成。转铁蛋白、胰岛素和孕酮是神经元培养中使用的因子。在这项研究中,我们确定了这些试剂对细胞辅酶Q和胆固醇水平的影响。转铁蛋白、胰岛素和孕酮的给药增加了未分化PC12细胞中的细胞辅酶Q水平。当去除血清并仅给予胰岛素时,细胞内辅酶Q水平增加。同时给予转铁蛋白、胰岛素和孕酮时,这种增加更为明显。转铁蛋白、胰岛素和孕酮的给药降低了胆固醇水平。孕酮处理以浓度依赖的方式降低细胞内胆固醇水平。我们的研究结果表明,转铁蛋白、胰岛素和孕酮可能有助于调节甲羟戊酸途径的产物辅酶Q水平和胆固醇水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5ff/10209592/2cec0643310c/jcbn22-115f01.jpg

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