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Perinatal nicotine-induced transgenerational asthma

机译:围产期尼古丁诱发的跨代哮喘

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摘要

Asthma is a major public health hazard worldwide. Its transgenerational inheritance has been inferred from epidemiological studies. More recently, using nicotine as a proxy for maternal smoking, we have demonstrated that an asthma-like phenotype can be inherited by rat offspring for up to two generations, i.e., multigenerationally, after the initial intrauterine exposure. We hypothesized that asthma transmission to offspring following perinatal nicotine exposure is not restricted up to F2 generation, but it also extends to subsequent generations. To test this hypothesis, using a well-established rat model of nicotine exposure-induced childhood asthma, we determined if perinatal nicotine exposure of F0 gestating dams would transmit asthma transgenerationally to F3 offspring. We now extend our findings to third-generation offspring, including abnormal pulmonary function, particularly as it relates to the occurrence in the upper airway exclusively in males, and to its effects on molecular functional markers (fibronectin and peroxisome proliferator-activated receptor γ), previously shown to be consistent with the asthma phenotype, herein expressed in fibroblasts isolated from the lung. These data, for the first time, demonstrate the transgenerational transmission of the asthma phenotype to F3 offspring following perinatal nicotine exposure of F0 dams.
机译:哮喘是全世界主要的公共健康危害。它的跨代遗传已经从流行病学研究中推断出来。最近,我们使用尼古丁作为孕产妇吸烟的替代物,我们已经证明,大鼠的后代可以在最初的宫内暴露后最多两代(即多代)遗传哮喘样表型。我们假设围产期尼古丁暴露后哮喘向后代的传播不仅限于F2代,而且还扩展到了后代。为了验证这一假设,我们使用建立良好的烟碱暴露诱发的儿童哮喘大鼠模型,我们确定了围产期F0妊娠母亲的烟碱暴露是否会导致哮喘向F3后代传代传播。现在,我们将研究结果扩展到第三代后代,包括异常的肺功能,特别是因为它与仅在男性中上呼吸道的发生有关,并且涉及其对分子功能标记(纤连蛋白和过氧化物酶体增殖物激活的受体γ)的影响,先前显示与哮喘表型一致,本文在从肺分离的成纤维细胞中表达。这些数据首次证明围产期尼古丁暴露于F0大坝后,哮喘表型向F3后代的跨代传播。

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