Lipid emulsion attenuates theophylline-induced cardiotoxicity in rat cardiomyoblasts.

IF 1.5 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Soo Hee Lee, Seung Hyun Ahn, Seong-Ho Ok, Gyujin Sim, Kyeong-Eon Park, Seunghyeon Park, Ju-Tae Sohn
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引用次数: 0

Abstract

Theophylline, a bronchodilator, induces cardiotoxicity due to its narrow therapeutic index. Lipid emulsion is used as a nonspecific antidote. However, its effects on theophylline-induced cardiotoxicity remain unknown. This study aimed to examine the effects of lipid emulsion on cardiotoxicity induced by toxic doses of theophylline in H9c2 rat cardiomyoblasts. The effects of theophylline and lipid emulsion (Lipofundin MCT/LCT), alone or in combination, on cell viability and migration were examined. Moreover, their effects on cleaved caspase-3, Bax/Bcl-XL ratio, and cleaved caspase-9 and caspase-8 expression, nuclear factor-κβ (NF-κβ) phosphorylation, and TUNEL-positive cells were examined. Theophylline treatment decreased cell viability. Lipofundin MCT/LCT (0.1-1%) with 50% longchain and 50% medium-chain fatty acids inhibited the theophylline-induced reduction in cell viability (3×10-3 M). It partially inhibited the theophylline-induced decrease in cell migration. Further, it reversed the theophylline-induced increase in cleaved caspase-3, Bax/Bcl-XL ratio, and cleaved caspase-9 expression as well as NF-κβ (Ser536) phosphorylation. However, theophylline treatment did not alter cleaved caspase-8 expression. Additionally, lipid emulsion inhibited theophylline-induced increase in TUNELpositive cells. Taken together, these results suggest that lipid emulsion reverses theophylline-induced apoptosis in cardiomyoblasts via inhibition of the mitochondrial apoptotic pathway associated with NF-κβ (Ser536) phosphorylation, indicating its potential for treating theophylline-induced cardiotoxicity.

脂质乳剂减轻茶碱诱导的大鼠成心肌细胞心脏毒性。
茶碱是一种支气管扩张剂,由于其治疗指数较窄而引起心脏毒性。脂质乳剂用作非特异性解毒剂。然而,其对茶碱诱导的心脏毒性的影响尚不清楚。本研究旨在探讨脂质乳对毒性剂量茶碱对H9c2大鼠成心肌细胞心脏毒性的影响。研究了茶碱和脂质乳(Lipofundin MCT/LCT)单独或联合使用对细胞活力和迁移的影响。并观察其对裂解型caspase-3、Bax/Bcl-XL比值、裂解型caspase-9和caspase-8表达、核因子-κβ (NF-κβ)磷酸化及tunel阳性细胞的影响。茶碱处理降低了细胞活力。含有50%长链和50%中链脂肪酸的Lipofundin MCT/LCT(0.1-1%)抑制茶碱诱导的细胞活力降低(3×10-3 M)。部分抑制茶碱诱导的细胞迁移减少。此外,它还逆转了茶碱诱导的裂解型caspase-3、Bax/Bcl-XL比值、裂解型caspase-9表达以及NF-κβ (Ser536)磷酸化的升高。然而,茶碱处理没有改变裂解caspase-8的表达。此外,脂质乳抑制茶碱诱导的tunel阳性细胞的增加。综上所述,这些结果表明,脂质乳通过抑制与NF-κβ (Ser536)磷酸化相关的线粒体凋亡途径,逆转了茶碱诱导的心肌细胞凋亡,表明其治疗茶碱诱导的心脏毒性的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
General physiology and biophysics
General physiology and biophysics 生物-生化与分子生物学
CiteScore
2.70
自引率
0.00%
发文量
42
审稿时长
6-12 weeks
期刊介绍: General Physiology and Biophysics is devoted to the publication of original research papers concerned with general physiology, biophysics and biochemistry at the cellular and molecular level and is published quarterly by the Institute of Molecular Physiology and Genetics, Slovak Academy of Sciences.
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