2012
DOI: 10.4067/s0716-97602012000200001
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In vitro assessment of reproductive toxicity of cigarette smoke and deleterious consequences of maternal exposure to its constituents

Abstract: Cigarette smoke is known to be a serious health risk factor and considered reproductively toxic. In the current study, we investigated whether constituents of cigarette smoke, pyrazine, 2-ethylpyridine, and 3-ethylpyridine, adversely aff ect reproductive functioning such as oocyte maturation and sperm capacitation. Our fi ndings indicated that three smoke components were involved in retardation of oocyte maturation in a dose-dependent manner and the lowest-observed-adverse-eff ect level (LOAEL) was determined … Show more

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Cited by 7 publications
(6 citation statements)
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“…Active smokers inhaled smoker directly from the cigarette, while passive smokers will inhale from other people's tobacco smoke. Various studies have shown that passive smoking has the same risk as active smokers for coronary heart disease, stroke, emphysema, lung cancer, and chronic lung disease [15][16][17] .…”
Section: Discussionmentioning
confidence: 99%
“…Active smokers inhaled smoker directly from the cigarette, while passive smokers will inhale from other people's tobacco smoke. Various studies have shown that passive smoking has the same risk as active smokers for coronary heart disease, stroke, emphysema, lung cancer, and chronic lung disease [15][16][17] .…”
Section: Discussionmentioning
confidence: 99%
“…Components of tobacco smoke will accumulate on the female reproductive organs 10,21 .…”
Section: Discussionmentioning
confidence: 99%
“…To capacitate sperm in vitro, samples were incubated in Whittingham medium supplemented with 10 mM HEPES and 4% BSA [Whittingham 1971] for 1 h under light mineral oil at 37 C in 5% C0 2 :95% air. Sperm capacitation status was assessed based on hyperactivation by objective photographic method [Wu and Liu 2012].…”
Section: Gamete and Embryo Collectionmentioning
confidence: 99%
“…Oocyte or preimplantation embryo samples were fixed in 4% paraformaldehyde made in DPBS, pH 7.4, for 30 min at room temperature [Wu and Liu 2012]. Samples were permeabillized by 0.1% Triton x-100 made in blocking solution (7.5 mg/mL glycine in PBS) for 5 min.…”
Section: Fluorescent Microscopymentioning
confidence: 99%