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1.
Eur Rev Med Pharmacol Sci ; 18(21): 3315-9, 2014.
Article in English | MEDLINE | ID: mdl-25487945

ABSTRACT

OBJECTIVE: Electronic cigarette smoking is gaining dramatic popularity and is steadily spreading among the adolescents, high income, urban population around the world. The aim of this study is to highlight the hazards of e-cigarette smoking on human health. MATERIALS AND METHODS: In this study, we identified 38 published studies through a systematic database searches including ISI-web of science and pub-med. We searched the related literature by using the key words including Electronic cigarette, E-cigarette, E-vapers, incidence, hazards. Studies in which electronic cigarette smoking hazards was investigated were included in the study. No limitations on publication status, study design of publication were implemented. Finally we included 28 publications and remaining 10 were excluded. RESULTS: E-smoking can cause, nausea, vomiting, headache, dizziness, choking, burn injuries, upper respiratory tract irritation, dry cough, dryness of the eyes and mucous membrane, release of cytokines and pro-inflammatory mediators, allergic airway inflammation, decreased exhaled nitric oxide (FeNO) synthesis in the lungs, change in bronchial gene expression and risk of lung cancer. CONCLUSIONS: Electronic cigarettes are swiftly promoted as an alternative to conventional cigarette smoking, although its use is highly controversial. Electronic cigarettes are not a smoking cessation product. Non-scientific claims about e-cigarettes are creating confusion in public perception about e-cigarette and people believe that e-cigarettes are safe and less addictive, but its use is unsafe and hazardous to human health. E-cigarette smoking should be regulated in the same way as traditional cigarettes and must be prohibited to children and adolescents.


Subject(s)
Electronic Nicotine Delivery Systems/adverse effects , Smoking/adverse effects , Adolescent , Child , Databases, Bibliographic , Humans
2.
Drugs Exp Clin Res ; 27(4): 127-33, 2001.
Article in English | MEDLINE | ID: mdl-11822222

ABSTRACT

Treatment with the drugs berenil, dibromopropamidine, pentamidine and CGP-4O-215 were found to alter levels of intracellular polyamines of Acanthamoeba polyphagia trophozoites in organisms. While the polyamine, spermidine, consistently remained higher in the control organisms incubated at 8, 16 and 32 h respectively, the level fluctuated significantly from below 5% to 40% in drug-treated organisms. A novel polyamine (polyamine F), yet to be identified, representing 80% of the total polyamine extracts and seen in control organisms after 48 h of incubation (stationary phase), was seen much earlier in the drug treated organisms. Pentamidine, dibromopropamidine and CGP-4O-215 induced the appearance of the novel polyamine in the trophozoites after only 8 h of incubation with the drugs while induction by berenil occurred after 32 h. It is suggested that diamidine drugs either induce encystment or alter the pathway of polyamine metabolism in Acanthamoeba. If inducing encystment is the main mode of reaction, then drugs that induce early encystment will be less effective in treatment than those that delay it.


Subject(s)
Acanthamoeba/drug effects , Antiprotozoal Agents/pharmacology , Diminazene/analogs & derivatives , Pentamidine/pharmacology , Polyamines/metabolism , Acanthamoeba/metabolism , Animals , Benzamidines/chemistry , Benzamidines/pharmacology , Diminazene/chemistry , Diminazene/pharmacology , Humans , Pentamidine/chemistry , Pyridines/chemistry , Pyridines/pharmacology , Robenidine/analogs & derivatives
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