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Effects of the HIV treatment drugs nevirapine and efavirenz on brain creatine kinase activity.
- Source :
-
Metabolic brain disease [Metab Brain Dis] 2008 Dec; Vol. 23 (4), pp. 485-92. Date of Electronic Publication: 2008 Sep 24. - Publication Year :
- 2008
-
Abstract
- Nevirapine (NVP) and efavirenz (EFV) are antiretroviral drugs belonging to potent class of non-nucleoside reverse transcriptase inhibitors (NNRTIs) widely used for the treatment human immunodeficiency virus (HIV) infection. It has been demonstrated that NVP and EFV are able to cross the blood-brain barrier and arrive at the central nervous system (CNS), causing important adverse effects related to their presence within this tissue. Considering that the exact mechanisms responsible for CNS toxicity associated with NVP and EFV remain unknown and that creatine kinase (CK) plays an important role in cell energy homeostasis, in the present work we evaluated CK activity in brain of mice after chronic administration of these drugs. Our results demonstrated that NVP and EFV significantly inhibited CK activity in cerebellum, hippocampus, striatum and cortex of mice. Although it is difficult to extrapolate our findings to the human condition, the inhibition of brain CK activity by NVP and EFV may be associated with neurological adverse symptoms of these drugs.
- Subjects :
- Alkynes
Animals
Blood-Brain Barrier drug effects
Brain drug effects
Cerebellum drug effects
Cerebellum enzymology
Cerebral Cortex drug effects
Cerebral Cortex enzymology
Creatine Kinase metabolism
Cyclopropanes
Enzyme Inhibitors pharmacology
Hippocampus drug effects
Hippocampus enzymology
Male
Mice
Neostriatum drug effects
Neostriatum enzymology
Reverse Transcriptase Inhibitors pharmacology
Anti-HIV Agents pharmacology
Benzoxazines pharmacology
Brain enzymology
Creatine Kinase drug effects
Nevirapine pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0885-7490
- Volume :
- 23
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Metabolic brain disease
- Publication Type :
- Academic Journal
- Accession number :
- 18815873
- Full Text :
- https://doi.org/10.1007/s11011-008-9109-2