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  • Lipoic acid prevents mirtaz...
    Oliveira, Tatiana de Queiroz; Chaves Filho, Adriano José Maia; Jucá, Paloma Marinho; Soares, Michelle Verde Ramos; Cunha, Natássia Lopes; Vieira, Charliene Freire Xavier; Gadelha Filho, Carlos Venício Jataí; Viana, Glautemberg de Almeida; De Oliveira, Gabriela Mariângela Farias; Macedo, Danielle Silveira; Vasconcelos, Silvânia Maria Mendes

    Behavioural brain research, 02/2022, Letnik: 419
    Journal Article

    Mirtazapine (MIRT) is a multi-target antidepressant used in treatment of severe depression with promising efficacy, but also with important side effects, mainly sedation and weight gain. Thus, the present study aimed to test the effects of the neuroprotective antioxidant lipoic acid (ALA) in the reversal of weight and metabolic changes induced by MIRT in corticosterone-induced depression model in mice, as well as proposed mechanisms for their association antidepressant and pro-cognitive effects. To do these male Swiss mice received Tween 80 (control), corticosterone (CORT 20 mg / kg), MIRT (3 mg / kg) and ALA (100 or 200 mg / kg), alone or associated for 21 days. After this, the animals were subjected to behavioral tests for affective and cognitive domains. Daily weight changes, blood cholesterol fractions and corticosterone were measured. Also, hippocampus (HC) protein expression of the serotonin transporter (SERT), synaptophysin, protein kinase B-Akt (total and phosphorylated) and the cytokines IL-4 and IL-6 were investigated. CORT induced a marked depression-like behavior, memory deficits, metabolic changes (total cholesterol and LDL) and increased serum corticosterone. Also, CORT increased SERT expression in the HC. MIRT alone or combined with ALA sustained its antidepressant-like effect, as well as reversed CORT-induced impairment in spatial recognition memory. Additionally, the association MIRT+ALA200 reversed the weight gain induced by the former antidepressant, as well as reduced serum corticosterone levels and SERT expression in the HC. ALA alone induced significant weight loss and reduced total cholesterol and HDL fraction. Our findings provide promising evidence about the ALA potential to prevent metabolic and weight changes associated to MIRT, without impair its antidepressant and pro-cognition actions. Therefore, ALA+MIRT combination could represent a new therapeutic strategy for treating depression with less side effects. •MIRT induced antidepressant-like effects in CORT model of depression.•MIRT and ALA in combination presented antidepressant-like effect in CORT model.•MIRT combined with ALA reversed MIRT-induced weight gain.•ALA presents anti-inflammatory effects in the brain.