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Meclofenoxate is a nootropic agent.1 It inhibits norepinephrine reuptake by isolated rat striatal synaptosomes (IC50 = 0.5 mM) and serotonin (5-HT) reuptake by isolated rat cortical synaptosomes (IC50 = 2.7 mM). Meclofenoxate increases survival of dopaminergic neurons in a C. elegans psd-1 knockdown model of Parkinson's disease.2 It reduces rotenone-induced depletion of dopamine and glutathione (GSH), lipid peroxidation, production of nitric oxide (NO), and cortical and cerebral damage, as well as enhances activity of catalase and superoxide dismutase in a rat model of Parkinson's disease when administered at a dose of 100 mg/kg.3 Meclofenoxate (100 mg/kg) increases synaptic surface density and reduces age-induced decreases in synaptic numerical density in aged rats.4 It also reduces neuronal lipofuscin pigment, a marker of aging, in the cerebral cortex and hippocampus and improves learning and memory in the T-maze in aged mice.5 Formulations containing meclofenoxate have been used in the treatment of senile dementia.
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1. Biogenic monoamine uptake by rat brain synaptosomes during aging. Effects of nootropic drugs. Gen. Pharmacol. 25(5), 981-987 (1994).
2. Chemical compensation of mitochondrial phospholipid depletion in yeast and animal models of parkinson’s disease. PLoS One 11(10), e0164465 (2016).
3. Effect of centrophenoxine against rotenone-
4. The effect of acute and chronic centrophenoxine treatment on the synaptic plasticity of old rats. Arch. Gerontol. Geriatr. 1(4), 365-373 (1982).
5. Centrophenoxine: Efects on aging mammalian brain. J. Am. Geriatr. Soc. 26(2), 74-81 (1978).