Literature DB >> 9546738

Identification of cigarette smoke components that alter functioning of hamster (Mesocricetus auratus) oviducts in vitro.

P Talbot1, G DiCarlantonio, M Knoll, C Gomez.   

Abstract

Previous studies have shown that solutions of mainstream and sidestream cigarette smoke decrease both ciliary beat frequency and oocyte cumulus complex pick-up rate of hamster oviducts in vitro. The purpose of this study was to identify the component(s) in smoke that produces these effects. Chemicals reported to be ciliotoxic in other systems were tested on hamster infundibula at various concentrations to determine whether a dose-response inhibition of ciliary beat frequency occurred. In addition, the concentration of each test component was measured in mainstream and sidestream smoke solutions (whole, particulate, and gas phase). All test components (acrolein, formaldehyde, phenol, acetaldehyde, and potassium cyanide [KCN]) inhibited ciliary beat frequency in a dose-dependent manner. Inhibition of ciliary beat frequency was at least partially reversible for all test compounds except acrolein. The concentrations of acrolein, formaldehyde, and phenol that were required to inhibit beat frequency were at least 3-50 times higher than their corresponding concentrations in smoke solutions. In contrast, cyanide was present in all smoke solutions at concentrations sufficient to inhibit ciliary beat frequency. Cilia on the outer surface of the infundibulum function in picking up the oocyte cumulus complex. Oocyte cumulus complex pick-up rate was measured in vitro at KCN concentrations shown to inhibit ciliary beat frequency. Pick-up rate was likewise inhibited by KCN and remained significantly depressed after washout of KCN. These data show that cyanide is a potent inhibitor of both ciliary beat frequency and oocyte cumulus complex pick-up rate and that its concentration in smoke solutions is sufficiently high to explain the previously reported inhibition of these oviductal processes.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9546738     DOI: 10.1095/biolreprod58.4.1047

Source DB:  PubMed          Journal:  Biol Reprod        ISSN: 0006-3363            Impact factor:   4.285


  7 in total

1.  A microRNA processing defect in smokers' macrophages is linked to SUMOylation of the endonuclease DICER.

Authors:  Thomas J Gross; Linda S Powers; Ryan L Boudreau; Brandi Brink; Anna Reisetter; Khushboo Goel; Alicia K Gerke; Ihab H Hassan; Martha M Monick
Journal:  J Biol Chem       Date:  2014-03-25       Impact factor: 5.157

2.  Characterization of oviduct ciliary beat frequency using real time phase resolved Doppler spectrally encoded interferometric microscopy.

Authors:  Youmin He; Yueqiao Qu; Joseph C Jing; Zhongping Chen
Journal:  Biomed Opt Express       Date:  2019-10-11       Impact factor: 3.732

Review 3.  Mechanism of Human Tubal Ectopic Pregnancy Caused by Cigarette Smoking.

Authors:  Quan Guo; Zaiyi Li; Steve Jia; Fangze Tong; Lin Ma
Journal:  Reprod Sci       Date:  2022-08-12       Impact factor: 2.924

4.  Histological study of smoke extract of Tobacco nicotiana on the heart, liver, lungs, kidney, and testes of male Sprague-Dawley rats.

Authors:  Adekomi Damilare Adedayo; A A Tijani; A A Musa; T D Adeniyi
Journal:  Niger Med J       Date:  2011-10

Review 5.  Smoking and reproduction: the oviduct as a target of cigarette smoke.

Authors:  Prue Talbot; Karen Riveles
Journal:  Reprod Biol Endocrinol       Date:  2005-09-28       Impact factor: 5.211

6.  Transcriptomic Evidence That Switching from Tobacco to Electronic Cigarettes Does Not Reverse Damage to the Respiratory Epithelium.

Authors:  Giovanna L Pozuelos; Meenakshi Kagda; Matine A Rubin; Maciej L Goniewicz; Thomas Girke; Prue Talbot
Journal:  Toxics       Date:  2022-07-04

7.  Pyrazine derivatives in cigarette smoke inhibit hamster oviductal functioning.

Authors:  Karen Riveles; Ryan Roza; Janet Arey; Prue Talbot
Journal:  Reprod Biol Endocrinol       Date:  2004-05-12       Impact factor: 5.211

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.