CART peptides and drugs of abuse : a review of recent progress

المؤلف

Kuhar, Michael J.

المصدر

Journal of Drug and Alcohol Research

العدد

المجلد 5، العدد 2016 (31 ديسمبر/كانون الأول 2016)، ص ص. 1-6، 6ص.

الناشر

Ashdin Publishing Corporation

تاريخ النشر

2016-12-31

دولة النشر

مصر

عدد الصفحات

6

التخصصات الرئيسية

علم الصيدلة

الموضوعات

الملخص EN

Earlier studies suggesting an involvement of cocaine and amphetamine regulated transcript peptide (CARTp) in the actions of drugs of abuse are confirmed in the most recent publications.

This seems especially true for the psychostimulants where CARTp in the nucleus accumbens inhibits or regulates the actions of these drugs; the regulation is lost after repeated drug use which may be an important mechanism in addiction.

The other drugs, including nicotine, alcohol, opiates, and perhaps caffeine can affect CARTp or CART mRNA levels.

While the exact mechanism is not always clear, the hope is that these findings may provide some insight for the development of medications.

While binding studies indicate the existence of specific G-protein coupled receptors (GPCR) receptors for CARTp,major work to be done is the cloning of these receptors

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Kuhar, Michael J.. 2016. CART peptides and drugs of abuse : a review of recent progress. Journal of Drug and Alcohol Research،Vol. 5, no. 2016, pp.1-6.
https://search.emarefa.net/detail/BIM-690783

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Kuhar, Michael J.. CART peptides and drugs of abuse : a review of recent progress. Journal of Drug and Alcohol Research Vol. 5 (2016), pp.1-6.
https://search.emarefa.net/detail/BIM-690783

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Kuhar, Michael J.. CART peptides and drugs of abuse : a review of recent progress. Journal of Drug and Alcohol Research. 2016. Vol. 5, no. 2016, pp.1-6.
https://search.emarefa.net/detail/BIM-690783

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 5-6

رقم السجل

BIM-690783