Contributing to Understand the Crosstalk between Brain and Periphery in Methylmercury Intoxication: Neurotoxicity and Extracellular Vesicles

被引:6
作者
Arrifano, Gabriela de Paula [1 ,2 ]
Augusto-Oliveira, Marcus [1 ,2 ]
Sealey-Bright, Megan [2 ]
Zainal, Jaezah [2 ]
Imbiriba, Luciana [1 ]
Pereira Fernandes, Luanna Melo [3 ]
Ferraz Maia, Cristiane Socorro [3 ]
Anthony, Daniel [2 ]
Crespo-Lopez, Maria Elena [1 ]
机构
[1] Univ Fed Para, Inst Ciencias Biol, Lab Farmacol Mol, BR-66075110 Belem, Para, Brazil
[2] Univ Oxford, Dept Pharmacol, Oxford OX1 3QT, England
[3] Fed Univ Para, Fac Pharm, Inst Hlth Sci, Lab Pharmacol Inflammat & Behav, BR-66075110 Belem, Para, Brazil
关键词
exosomes; mercury; MeHg; exposure; pollution; pollutant; CNS; S100b; real time; qPCR; MERCURY; EXPOSURE; S100B; EXPRESSION; GLUTAMATE; EXOSOMES; INVOLVEMENT; CEREBELLUM; PROTEINS; DISEASE;
D O I
10.3390/ijms221910855
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human exposure to methylmercury (MeHg) is currently high in regions such as the Amazon. Understanding the molecular changes associated with MeHg-induced neurotoxicity and the crosstalk with the periphery is essential to support early diagnoses. This work aimed to evaluate cellular and molecular changes associated with behavioral alterations in MeHg acute exposure and the possible changes in extracellular vesicles (EVs) number and S100 beta content. Adults male Wistar rats were orally treated with 5 mg/kg for four days. Behavioral performance, molecular and histological changes in the cerebellum, and plasma EVs were assessed. MeHg-intoxicated animals performed significantly worse in behavioral tests. MeHg increased the number of GFAP+ cells and GFAP and S100 beta mRNA expression in the cerebellum but no change in NeuN+ or IBA-1+ cells number was detected. The number of exosomes isolated from plasma were decreased by the metal. S100B mRNA was detected in circulating plasma EVs cargo in MeHg exposure. Though preliminary, our results suggest astrocytic reactivity is displaying a protective role once there was no neuronal death. Interestingly, the reduction in exosomes number could be a new mechanism associated with MeHg-induced neurotoxicity and plasma EVs could represent a source of future biomarkers in MeHg intoxication.
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页数:16
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