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[Effect of perfluorooctanoic acid on lipid accumulation in rat liver cells BRL-3A and its possible mechanism].
Sun, Weiqiang; Ma, Xinzhuang; Zhou, Yongbing; Wang, Li; Liu, Hui.
Afiliación
  • Sun W; School of Laboratory Medicine, Bengbu Medical College, Anhui Province Key Laboratory of Immunology in Chronic Diseases, Bengbu 233030, China.
  • Ma X; School of Public Health, Bengbu Medical College, Anhui Province Key Laboratory of Immunology in Chronic Diseases, Bengbu 233030, China.
  • Zhou Y; School of Public Health, Bengbu Medical College, Anhui Province Key Laboratory of Immunology in Chronic Diseases, Bengbu 233030, China.
  • Wang L; School of Public Health, Bengbu Medical College, Anhui Province Key Laboratory of Immunology in Chronic Diseases, Bengbu 233030, China.
  • Liu H; School of Laboratory Medicine, Bengbu Medical College, Anhui Province Key Laboratory of Immunology in Chronic Diseases, Bengbu 233030, China.
Wei Sheng Yan Jiu ; 51(1): 107-112, 2022 Jan.
Article en Zh | MEDLINE | ID: mdl-35341501
OBJECTIVE: To investigate the effect of perfluorooctanoic acid on rat hepatocytes BRL-3 A cell viability and the expression of transcription factor nuclear factor erythroid 2-related factor 2(Nrf2) and arginosuccinate synthase(Ass1). METHODS: Rat hepatocytes BRL-3 A were cultured and divided into control group(0 µmol/L PFOA), low-dose group(6.25 µmol/L PFOA), and medium-dose group(25 µmol/L PFOA), high-dose group(100 µmol/L PFOA). After 48 hours, cell viability was detected by MTT, ROS content was detected by free radical indicator H_2DCFDA, enzyme activity related to oxidative stress was detected by the kit, Nrf2 and Ass1 protein expression level was detected by Western blot and immunocytochemistry(ICC). RESULTS: Compared with the control group, with the increase of the PFOA concentration, the cell viability of the middle and high dose groups had a downward trend, but there was no statistical significance(P>0.05). The intracellular ROS content increased, among which in the middle and high dose groups significantly increased(P<0.05), and the average fluorescence intensity was(5417.66±161.09) and(5725.50±166.83), respectively. Compared with the control group, the content of intracellular TG, TC and MDA in the low and medium dose groups did not change significantly, and the content of TG, TC and MDA in the high dose group was significantly increased(P<0.05), which was(0.21±0.05) mmol/L, (14.5±6.07) mmol/L and(1.23±0.33) nmol/mL, respectively. According to the ICC and Western blot result, the expression level of Nrf2 protein increased significantly in the high-dose group(P<0.05), and the expression level of Ass1 protein increased significantly in the low-dose group(P<0.05). CONCLUSION: Exposure to a certain dose of PFOA can lead to the accumulation of ROS in BRL-3 A cells. Nrf2 and Ass1 can play a certain role in eliminating ROS and ammonia detoxification by increasing their expression under the oxidative damage of rat liver cells caused by PFOA.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Caprilatos / Fluorocarburos Límite: Animals Idioma: Zh Revista: Wei Sheng Yan Jiu Asunto de la revista: SAUDE PUBLICA Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Caprilatos / Fluorocarburos Límite: Animals Idioma: Zh Revista: Wei Sheng Yan Jiu Asunto de la revista: SAUDE PUBLICA Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: China