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Anthroponosis (human to animal transmission) and reverse anthroponosis (spill-over back into humans after a period of adaptation in the new animal reservoir) have been detected for SARS-CoV-2, thus impeding the eradication of SARS-CoV-2 and increasing the risks of recombination, evolution and immune evasion [15]

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In vivo, chronic intraperitoneal MG administration, particularly in the context of morphine exposure, increased CB1 receptor expression in the hippocampal CA1 region and ventral tegmental area [24]