A comparison study of effects of Echinacea extract and levamisole on phenytoin-induced cleft palate in mice
There are many reports that the teratogenic effects of phenytoin, especially cleft palate can be decreased by stimulation of maternal immune system. Also, there is some evidence that Echinacea extract and levamisole are immunomodulator drugs. So, in this study, we compared the prophylactic effects o...
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Veröffentlicht in: | Regulatory toxicology and pharmacology 2006-12, Vol.46 (3), p.163-166 |
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Zusammenfassung: | There are many reports that the teratogenic effects of phenytoin, especially cleft palate can be decreased by stimulation of maternal immune system. Also, there is some evidence that
Echinacea extract and levamisole are immunomodulator drugs. So, in this study, we compared the prophylactic effects of levamisole and
Echinacea extract on teratogenic effects of phenytoin. This study was performed on 32 pregnant mice that were divided into four groups. The first group (control group) received normal saline intraperitoneally and the other groups (test groups) received phenytoin (65
mg/kg intraperitoneally) at 10th day of gestation. Levamisole and extract of
Echinacea purpurea were administrated at dose of 10 and 360
mg/kg intraperitoneally, respectively, in along with and 12
h later after phenytoin injection, in two groups. Fetuses were carried out in 19th day of gestation and after determination of weight and length; they were stained by Alizarin red–Alcian blue method. Cleft palate incidence was 16, 5.3, and 3.2% in fetuses of mice that received only phenytoin, phenytoin with levamisole, and phenytoin with
Echinacea extract, respectively. Mean weight and length of fetuses of animals that received levamisole and
Echinacea extract were significantly greater than those received only phenytoin. It is concluded that
Echinacea can stimulate immune system more than levamisole and has better prophylactic effect on incidence of phenytoin-induced cleft palate, but it is not significant. |
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ISSN: | 0273-2300 1096-0295 |
DOI: | 10.1016/j.yrtph.2006.06.005 |