Latrepirdine dihydrochloride (Dimebolin dihydrochloride) is an orally active, and neuroactive antagonist of multiple drug targets, including histamine receptors, GluR, and 5-HT receptors, used as an antihistamine drug.

Latrepirdine increases succinate dehydrogenase activity (MTT-assay), mitochondrial membrane potential (DeltaPsim), and cellular ATP levels in primary mouse cortical neurons and human neuroblastoma cells (SH-SY5Y). Latrepirdine enhances mitochondrial function both in the absence and presence of stress and Dimebon-treated cells are partially protected to maintain cell viability. [1] Latrepirdine leads to enhanced mTOR- and Atg5-dependent autophagy in cultured mammalian cells. [2] latrepirdine stimulates MTOR- and ATG5-dependent autophagy, leading to the reduction of intracellular levels of APP metabolites, including Aβ in cultured cells. [3] Latrepirdine stimulates the degradation of α-syn in differentiated SH-SY5Y neurons, and in mouse brain following chronic administration, in parallel with elevation of the levels of markers of autophagic activity. [4] Latrepirdine increases intracellular ATP levels and glucose transporter 3 translocation to the plasma membrane in primary neuron. [5]

Latrepirdine treatment of TgCRND8 transgenic mice is linked to improved learning behavior and reduced accumulation of Aβ42 and α-synuclein. [2] Latrepirdine administration results in increased levels of biomarkers associated with autophagy activation in the brains of TgCRND8 (APP K670M, N671L, V717F) or wild-type mice, and is also associated with behavioral improvement, reduced Aβ neuropathology, and prevention of autophagic failure in TgCRND8 mice. [3]

DMSO: 39.2 mg/mL (99.91 mM), Sonication is recommended.

10% DMSO+40% PEG300+5% Tween-80+45% Saline: 0.5 mg/mL (1.27 mM), Sonication is recommended.