کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6281331 | 1615111 | 2015 | 6 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Potential involvement of the mitochondrial unfolded protein response in depressive-like symptoms in mice
ترجمه فارسی عنوان
دخالت بالقوه پاسخ پروتئین باز شدن میتوکندریال در علائم افسردگی در موش
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
کلمات کلیدی
ADPUPRmtMitochondrial DNA - DNA میتوکندریاROS - ROSadenosine diphosphate - آدنوزین دی فسفاتMajor depression - افسردگی شدیدstandard error - خطای استانداردmtDNA - دیانای میتوکندریاییDepressive-like behavior - رفتار افسردگی مانندMitochondria - میتوکندریاmitochondrial unfolded protein response - پاسخ پروتئین بازتابنده میتوکندریReactive oxygen species - گونههای فعال اکسیژن
موضوعات مرتبط
علوم زیستی و بیوفناوری
علم عصب شناسی
علوم اعصاب (عمومی)
چکیده انگلیسی
Many evidences strongly suggest that a mitochondrial deficit is implicated in major depression. A mitochondrial deficit leads to mitochondrial stress responses, including the mitochondrial unfolded protein response (UPRmt), which is associated with certain brain disorders such as spastic paraplegia and Parkinson's disease. However, there is no evidence regarding the relationship between depressive disorder and UPRmt. Mice treated with chronic restraint stress showed significant depressive-like behaviors in the tail suspension and forced swim tests, decreased oxygen consumption rate, and increased levels of molecules associated with UPRmt such as Hspa9, Hspd1, Ubl5, Abcb10, and ClpP. All of the UPRmt-related molecules were significantly correlated with depressive-like behavior in the forced swim test. Thus, the present study is to reveal a relationship between the UPRmt and depressive disorder, suggesting that the UPRmt is a potential drug target for depressive disorders.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuroscience Letters - Volume 588, 19 February 2015, Pages 166-171
Journal: Neuroscience Letters - Volume 588, 19 February 2015, Pages 166-171
نویسندگان
Yuki Kambe, Atsuro Miyata,