Methamphetamine is, worldwide, one of the most consumed drugs of abuse. One important side effect is neurodegeneration leading to a decrease in life expectancy. The aim of this paper was to check whether the drug affects one of the receptors involved in neurodegeneration/neuroprotection events, namely the adenosine A receptor (AR). First, we noticed that methamphetamine does not affect A functionality if the receptor is expressed in a heterologous system. However, AR becomes sensitive to the drug upon complexes formation with the cannabinoid CB receptor (CBR) and the sigma 1 receptor (σR). Signaling via both adenosine AR and cannabinoid CBR was affected by methamphetamine in cells co-expressing the two receptors. In striatal primary cultures, the AR-CBR heteromer complex was detected and methamphetamine not only altered its expression but completely blocked the AR- and the CBR-mediated activation of the mitogen activated protein kinase (MAPK) pathway. In conclusion, methamphetamine, with the participation of σR, alters the expression and function of two interacting receptors, AR, which is a therapeutic target for neuroprotection, and CBR, which is the most abundant G protein-coupled receptor (GPCR) in the brain.
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http://dx.doi.org/10.3390/ijms22052743 | DOI Listing |
Int J Rheum Dis
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The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, Anhui, China.
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December 2024
State Key Laboratory of Tree Genetics and Breeding, College of Biological Sciences and Technology, Beijing Forestry University, Beijing 100083, China.
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View Article and Find Full Text PDFChin J Integr Med
January 2025
Department of Ultrasound in Medicine, the Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, 310009, China.
Objective: To evaluate the therapeutic effects of Kuanxiong Aerosol (KXA) on ischemic stroke with reperfusion and elucidate the underlying pharmacological mechanisms.
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Cells
January 2025
Department of Pharmacology, University of Oxford, Mansfield Road, Oxford OX1 3QT, UK.
Sandhoff disease (SD) is a progressive neurodegenerative lysosomal storage disorder characterized by GM2 ganglioside accumulation as a result of mutations in the gene, which encodes the β-subunit of the enzyme β-hexosaminidase. Lysosomal storage of GM2 triggers inflammation in the CNS and periphery. The NLRP3 inflammasome is an important coordinator of pro-inflammatory responses, and we have investigated its regulation in murine SD.
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Department of Pharmacology, School of Basic Medical Sciences, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Joint International Research Laboratory of Sleep, Fudan University, Shanghai, 200032, China.
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