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Mol Cell Endocrinol ; 524: 111157, 2021 03 15.
Artigo em Inglês | MEDLINE | ID: mdl-33421531

RESUMO

Both the cholinergic pathway and oxidative stress are important mechanisms involved in the pathogenesis of hypothyroidism, a condition characterized by low levels of thyroid hormone that predispose the patient to brain dysfunction. Phenolic compounds have numerous health benefits, including antioxidant activity. This study evaluates the preventive effects of resveratrol in the cholinergic system and redox status in rats with methimazole-induced hypothyroidism. Hypothyroidism increases acetylcholinesterase (AChE) activity and density in the cerebral cortex and hippocampus and decreases the α7 and M1 receptor densities in the hippocampus. Hypothyroidism also increases cellular levels of reactive oxygen species (ROS) and thiobarbituric acid reactive substances (TBARS), but reduces total thiol content, and catalase and superoxide dismutase activities in the serum. In the cerebral cortex and hippocampus, hypothyroidism increases the levels of ROS and nitrites. In this study, resveratrol (50 mg/kg) treatment prevents the observed increase in AChE in the cerebral cortex, and increases the protein levels of NeuN, a marker of mature neurons. Resveratrol also prevents changes in serum ROS levels and brain structure, as well as the levels of TBARS, total thiol content, and serum catalase enzyme activity. These collective findings suggest that resveratrol has a high antioxidant capacity and can restore hypothyroidism-triggered alterations related to neurotransmission. Thus, it is a promising agent for the prevention of brain damage resulting from hypothyroidism.


Assuntos
Colinérgicos/metabolismo , Hipotireoidismo/metabolismo , Hipotireoidismo/patologia , Neuroproteção/efeitos dos fármacos , Resveratrol/farmacologia , Transdução de Sinais , Acetilcolinesterase/metabolismo , Animais , Antígenos Nucleares/metabolismo , Modelos Animais de Doenças , Proteína Glial Fibrilar Ácida/metabolismo , Hipocampo/metabolismo , Hipotireoidismo/sangue , Masculino , Proteínas do Tecido Nervoso/metabolismo , Oxirredução/efeitos dos fármacos , Estresse Oxidativo/efeitos dos fármacos , Ratos Wistar , Receptores Colinérgicos/metabolismo , Transdução de Sinais/efeitos dos fármacos , Tiroxina/sangue , Tri-Iodotironina/sangue
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