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Apoptosis induced by acrylamide is suppressed in a 21.5 fat diet through caspase-3-independent pathway in mice testis

机译:21.5%的脂肪饮食中通过caspase-3非依赖性途径抑制了小鼠睾丸中丙烯酰胺诱导的细胞凋亡。

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摘要

This study investigates the simultaneous effect of acrylamide (ACR) and high-fat-intake on the apoptosis in testis cells, and also the expression and activity of caspase-3. Seventy-two male Kunming mice were divided into two blocks and fed with a high-fat diet (crude fat 21.5%) or basic diet (crude fat 4.4%), respectively; and animals in each diet block were exposed to ACR at the dose of 20 mg/kgbw•d or 40 mg/kgbw•d as ACR treated groups or the normal saline as control. Germ cells prepared from testis were stained with Hoechst dye 33258 and paraffin wax sections from testis were suffered to a TUNEL process. Expression of caspase-3 on protein level was investigated using an immunohistochemical analysis assay. The supernatant of unilateral testes were subjected to a Caspase-3 activity kit to determine the activity of Caspase-3 in testis. The concentration of ACR and glycidamide(GA), epox-ide of ACR, in plasma and testis were detected by LC-ES/MS/MS analysis. Results based on the morphological changes, percentage of apoptotic cells, and integrated optical density (IOD) of positive amethyst staining which indicates the apoptotic DNA fragmentation, show that apoptosis was induced by acrylamide only; however, acr-ylamide-induced apoptosis was weakened by high-fat-intake. The protein expression and activity of Caspase-3 were not induced by ACR or high-fat-intake. Moreover, no significant differences of ACR and GA concentration were found between the high-fat and basic diet groups after exposure of ACR. Results indicate that high-fat-intake reverses the effects on apoptosis induced by ACR; and more possibly, apoptosis is induced by a caspase-3-independent mechanism.
机译:这项研究调查了丙烯酰胺(ACR)和高脂摄入对睾丸细胞凋亡的同时影响,以及caspase-3的表达和活性。将七十二只昆明雄性小鼠分为两个部分,分别喂养高脂饮食(粗脂肪21.5%)或基本饮食(粗脂肪4.4%);并且将每个饮食块中的动物作为ACR治疗组,以20 mg / kgbw•d或40 mg / kgbw•d的剂量暴露于ACR,或将生理盐水作为对照组。睾丸制备的生殖细胞用Hoechst染料33258染色,睾丸的石蜡切片经TUNEL处理。使用免疫组织化学分析方法研究了caspase-3在蛋白水平上的表达。将单侧睾丸的上清液置于Caspase-3活性试剂盒中,以确定睾丸中Caspase-3的活性。通过LC-ES / MS / MS分析检测血浆和睾丸中ACR和缩水甘油酰胺(GA),ACR的环氧化物的浓度。根据形态变化,凋亡细胞百分数和阳性紫水晶染色的积分光密度(IOD)(表明凋亡DNA片段化)得出的结果表明,凋亡仅由丙烯酰胺诱导。然而,高脂摄入会削弱丙烯酰胺诱导的细胞凋亡。 ACR或高脂摄入不会诱导Caspase-3的蛋白表达和活性。此外,在高脂饮食组和基本饮食组中,ACR暴露后,ACR和GA浓度没有显着差异。结果表明,高脂摄入可以逆转ACR诱导的细胞凋亡。更有可能的是,细胞凋亡是由不依赖caspase-3的机制诱导的。

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