کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8516223 | 1556574 | 2018 | 45 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Maladaptive behavioral regulation in alcohol dependence: Role of kappa-opioid receptors in the bed nucleus of the stria terminalis
ترجمه فارسی عنوان
مقررات رفتاری ناسازگارانه در وابستگی به الکل: نقش گیرنده های کاپا اپیوئید در هسته بستر ترمینال های استری
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کلمات کلیدی
EPMBed nucleus of the stria terminalis (BNST)OPRK1USVBNSTpDynMORultrasonic vocalization - آوازگیری اولتراسونیکSelf administration - اداره خودAlcohol withdrawal - ترک الکلOperant self-administration - خود اداره عملیاتdynorphin - دینورفینDyn - مردNor-BNI - نور BNINor-binaltorphimine - نور باینلورفیمیمbed nucleus of the stria terminalis - هسته تخت ترمینال های استریAlcohol dependence - وابستگی الکلیKOR - وقتیkappa opioid receptor - گیرنده اپوئیدی کاپاپkappa-opioid receptor - گیرنده کاپا اپیوئیدmu-opioid receptor - گیرنده ی مئو-اپوئیدی
موضوعات مرتبط
علوم زیستی و بیوفناوری
علم عصب شناسی
علوم اعصاب رفتاری
چکیده انگلیسی
There is an important emerging role for the endogenous opioid dynorphin (DYN) and the kappa-opioid receptor (KOR) in the treatment of alcohol dependence. Evidence suggests that the DYN/KOR system in the bed nucleus of the stria terminalis (BNST) contributes to maladaptive behavioral regulation during withdrawal in alcohol dependence. The current experiments were designed to assess dysregulation of the BNST DYN/KOR system by evaluating alcohol dependence-induced changes in DYN/KOR gene expression (Pdyn and Oprk1, respectively), and the sensitivity of alcohol self-administration, negative affective-like behavior and physiological withdrawal to intra-BNST KOR antagonism during acute withdrawal. Wistar rats trained to self-administer alcohol, or not trained, were subjected to an alcohol dependence induction procedure (14â¯h alcohol vapor/10â¯h air) or air-exposure. BNST micropunches from air- and vapor-exposed animals were analyzed using RT-qPCR to quantify dependence-induced changes in Pdyn and Oprk1 mRNA expression. In addition, vapor- and air-exposed groups received an intra-BNST infusion of a KOR antagonist or vehicle prior to measurement of alcohol self-administration. A separate cohort of vapor-exposed rats was assessed for physiological withdrawal and negative affective-like behavior signs following intra-BNST KOR antagonism. During acute withdrawal, following alcohol dependence induction, there was an upregulation in Oprk1 mRNA expression in alcohol self-administering animals, but not non-alcohol self-administering animals, that confirmed dysregulation of the KOR/DYN system within the BNST. Furthermore, intra-BNST KOR antagonism attenuated escalated alcohol self-administration and negative affective-like behavior during acute withdrawal without reliably impacting physiological symptoms of withdrawal. The results confirm KOR system dysregulation in the BNST in alcohol dependence, illustrating the therapeutic potential of targeting the KOR to treat alcohol dependence.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuropharmacology - Volume 140, 15 September 2018, Pages 162-173
Journal: Neuropharmacology - Volume 140, 15 September 2018, Pages 162-173
نویسندگان
Chloe M. Erikson, Gengze Wei, Brendan M. Walker,