Chronic Alcohol Intoxication and Cortical Ischemia: Study of Their Comorbidity and the Protective Effects of Minocycline

Author:

Fontes-Júnior Enéas Andrade12ORCID,Maia Cristiane Socorro Ferraz2ORCID,Fernandes Luanna Melo Pereira2,Gomes-Leal Walace3,Costa-Malaquias Allan1ORCID,Lima Rafael Rodrigues4,Prediger Rui Daniel5,Crespo-López Maria Elena1

Affiliation:

1. Laboratory of Molecular Pharmacology, Institute of Biological Sciences, Federal University of Pará, 66075-110 Belém, PA, Brazil

2. Laboratory of Pharmacology of Inflammation and Behavior, Institute of Health Sciences, Federal University of Pará, 66075-110 Belém, PA, Brazil

3. Laboratory of Experimental Neuroprotection and Neurodegeneration, Institute of Biological Sciences, Federal University of Pará, 66075-110 Belém, PA, Brazil

4. Laboratory of Functional and Structural Biology, Institute of Biological Sciences, Federal University of Pará, 66075-110 Belém, PA, Brazil

5. Department of Pharmacology, Center of Biological Sciences, Federal University of Santa Catarina, 88040-900 Florianópolis, SC, Brazil

Abstract

Chronic alcohol intoxication (CAI) increases both morbidity and mortality of stroke patients. Despite the high prevalence of CAI and ischemic stroke, studies addressing their comorbidity and/or protective alternatives remain scarce. Thus, the influence of CAI on both stroke outcome and minocycline treatment (recognized for its neuroprotective effect) was investigated. Female Wistar rats (35 days old) were treated with water or ethanol (6.5 g/kg/day, 22.5% w/v) for 55 days. Then, focal ischemia was induced by endothelin-1 in the motor cortex. Two hours later, four doses of 50 mg/kg of minocycline every 12 hours followed by five doses of 25 mg/kg every 24 hours were administered. Behavioral performance (open field and rotarod tests) and immunohistochemical (cellular density, neuronal death, and astrocytic activation) and biochemical (lipid peroxidation and nitrite levels) analyses were performed. CAI increased motor disruption, nitrite and lipid peroxidation levels, and neuronal loss caused by ischemia, whereas it reduced the astrogliosis. Minocycline was effective in preventing the motor and tissue damage caused by stroke. However, these effects were attenuated when CAI preceded stroke. Our data suggest that CAI beginning in adolescence contributes to a worse outcome in ischemic stroke survivors and reduces the benefits of minocycline, possibly requiring adjustments in therapy.

Funder

Fundação de Amparo à Pesquisa do Estado da Bahia

Publisher

Hindawi Limited

Subject

Cell Biology,Aging,General Medicine,Biochemistry

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