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咀嚼功能负荷增加大鼠咬肌中ACTN2和ACTN3的mRNA表达水平以及α-辅肌动蛋白-2的蛋白表达。

Masticatory Functional Load Increases the mRNA Expression Levels of ACTN2 and ACTN3 and the Protein Expression of α-Actinin-2 in Rat Masseter Muscle.

作者信息

Masita Silviana Nur, Andarini Sri, Lyrawati Diana, Hidayat Mohammad

机构信息

Universitas Brawijaya Faculty of Dentistry, Department of Orthodontics, Malang, Indonesia.

Universitas Brawijaya Faculty of Medicine, Department of Public Health, Malang, Indonesia.

出版信息

Turk J Pharm Sci. 2021 Feb 25;18(1):28-33. doi: 10.4274/tjps.galenos.2019.53323.

Abstract

OBJECTIVES

α-actinins play structural and regulatory roles in cytoskeletal organization. They form a lattice structure that secures actin in thin filaments, which generate and transmit muscle contractile forces. The morphological and biochemical characteristics of rat masseter muscles are known to change reactions to masticatory functional loads, but their effect on α-actinins remains unknown. This study aimed to determine the response of α-actinins to masticatory functional loads.

MATERIALS AND METHODS

Twenty-four male Wistar rats aged 3 weeks were divided randomly into 3 groups of liquid diet (LD), soft diet, and hard diet (HD). The rats were then sacrificed at the end of 8 weeks. The middle part of superficial masseter muscles was examined to investigate the masticatory effect of functional load on the mRNA expression levels of ACTN2 and ACTN3 and the protein expression levels of α-actinin-2 and α-actinin-3.

RESULTS

The mRNA expression levels of ACTN2 and ACTN3 and the protein expression levels of α-actinin-2 of the HD group were significantly higher than those of the LD group, which served as the control group.

CONCLUSION

Masticatory functional load organizes the mRNA expression levels of ACTN2 and ACTN3 and the protein expression levels of α-actinin-2 in rat masseter muscles through stimuli during muscle physiological adaptation.

摘要

目的

α-辅肌动蛋白在细胞骨架组织中发挥结构和调节作用。它们形成一种晶格结构,将肌动蛋白固定在细肌丝中,细肌丝产生并传递肌肉收缩力。已知大鼠咬肌的形态和生化特征会因咀嚼功能负荷而发生变化,但其对α-辅肌动蛋白的影响尚不清楚。本研究旨在确定α-辅肌动蛋白对咀嚼功能负荷的反应。

材料与方法

将24只3周龄雄性Wistar大鼠随机分为流食(LD)、软食和硬食(HD)3组。8周结束时处死大鼠。检查咬肌浅层中部,以研究功能负荷对ACTN2和ACTN3 mRNA表达水平以及α-辅肌动蛋白-2和α-辅肌动蛋白-3蛋白表达水平的咀嚼作用。

结果

HD组的ACTN2和ACTN3 mRNA表达水平以及α-辅肌动蛋白-2的蛋白表达水平显著高于作为对照组的LD组。

结论

咀嚼功能负荷通过肌肉生理适应过程中的刺激,调节大鼠咬肌中ACTN2和ACTN3的mRNA表达水平以及α-辅肌动蛋白-2的蛋白表达水平。

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本文引用的文献

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ACTN3 R577X genotypes associate with Class II and deepbite malocclusions.α-辅肌动蛋白3基因R577X基因型与Ⅱ类错颌畸形和深覆颌有关。
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alpha-actinin-3 and performance.α-辅肌动蛋白-3与运动表现。
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