کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8338004 | 1540985 | 2016 | 8 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
A microsomal based method to detect aromatase activity in different brain regions of the rat using ultra performance liquid chromatography-mass spectrometry
ترجمه فارسی عنوان
یک روش مبتنی بر میکروسومال برای تشخیص فعالیت آروماتاز در مناطق مختلف مغز موش صحرایی با استفاده از طیف سنجی جرمی کروماتوگرافی مایع فوق العاده
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موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
زیست شیمی
چکیده انگلیسی
Aromatase (ARO) is a cytochrome P450 enzyme that accounts for local estrogen production in the brain. The goal of this study was to develop a microsomal based assay to sensitively and reliably detect the low levels of ARO activity in different brain regions. Enzyme activity was detected based on the conversion of testosterone to estradiol. Quantity of estradiol was measured using ultra performance liquid chromatography-mass spectrometry. Detection was linear over a range of 2.5-200Â pg/ml estradiol, and was reproducible with intra- and inter-assay coefficients of variation (CV) <15%. Estradiol production using isolated microsomes was linear with time up to 30Â min as well as linearly related to amount of microsome. Substrate concentration curves revealed enzymatic kinetics (hippocampus: Vmax and Km: 0.57Â pmol estradiol/h per mg microsome and 48.58Â nM; amygdala: Vmax and Km: 1.69Â pmol estradiol/h per mg microsome and 48.4Â nM; preoptic area: Vmax and Km: 0.96Â pmol estradiol/h per mg microsome and 44.31Â nM) with testosterone used at a saturating concentration of 400Â nM. Anastrozole treatment blocked ARO activity in hippocampal and ovarian microsomes, indicating that the assay is specific for ARO. Also, we showed that the distribution of the long form ARO mRNA (CYP19A1) in different regions of the brain is correlated with ARO activity, with highest levels in the amygdala, followed by preoptic area and hippocampus. In the frontal cortex, very little long form ARO mRNA, and little to no ARO activity, were detected. These findings demonstrate that the microsomal incubation (MIB) assay is a sensitive and reliable method for quantifying ARO activity in discrete brain regions.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: The Journal of Steroid Biochemistry and Molecular Biology - Volume 163, October 2016, Pages 113-120
Journal: The Journal of Steroid Biochemistry and Molecular Biology - Volume 163, October 2016, Pages 113-120
نویسندگان
Junyi Li, Patrick J. Oberly, Samuel M. Poloyac, Robert B. Gibbs,