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M.T. Goghataei, F. Kermanian, M. Mehdizadeh. Anatomy Department, Iran University, Tehran, Iran Peganum Harmala is popular plant in traditional medicine. It used for the treatment of asthma, parasitical and microbial infections, postpartum hemorrhage and etc. In order to study the side effects of PJHL in pregnant mice such as growth retardation and abortion, we injected P.H. intraperitoneally to the pregnant mice in three doses: 6, 15, 30 mg kg day from the first up to the lo"h day of pregnancy, then we killed the mice in 1519" pregnancy days. After Laparatomy we extract fetuses and measured their height and weight. Then the fetuses were stained with Alizarin Red and observed with stereomicroscope for skeletal anomalies. Conclusions showed that there were no skeletal anomalies. But in comparison with control group, absorption and decrease of height and weight was observed. Since the most absorption of the fetuses was in the last days of pregnancy 1819th ; , we believe that P.H. causes abortion by means of affecting on growth and development offetus. 242 and zyloprim.

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SELECT-1 Antiviral Results The study has been completed for the 160, 320 and 480 g dose cohorts of the study. The 12week antiviral results for the two Locteron doses that were most effective, the 320 and 480 g doses, compare favorably with results previously reported in clinical trials for the currently marketed pegylated interferon alfa products and for Albuferon. At the conclusion of the study, 12 weeks of treatment, the results for the 160, 320 and 480 g dose cohorts were as follows: A dose response was observed in the study, with patients treated with the 320 and 480 g doses of Locteron demonstrating a greater reduction in hepatitis C virus than the patients treated with the 160 g dose at all measurement times. Average viral reduction after 12 weeks of treatment for the 320 and 480 g doses was 4.5 and 4.2 logs, respectively, compared to 1.8 logs in the lowest dose of 160 g. After 12 weeks of treatment, plasma hepatitis C RNA was reduced to undetectable levels 28 IU ml ; 63% 5 8 ; and 63% 5 8 ; of the patients in the 320 and 480 g dose cohorts, respectively, compared to 13% 1 8 ; of the patients in the lowest-dose group of 160 g. The percentage of patients who achieved early virologic response EVR ; , defined as at least a two-log reduction in hepatitis C virus after 12 weeks of treatment, was 88% 7 8 ; and 100% 8 ; in the 320 and 480 g dose cohorts, respectively, compared to 38% 3 8 ; of the patients in the lowest-dose group of 160 g. Achievement of EVR has been broadly established to be a pre-requisite for long-term response. SELECT-1 Safety and Tolerability Results The following Locteron side effect and patient tolerability results were observed during the 12 weeks of treatment for the 160, 320 and 480 g dose cohorts: Locteron was safe and well tolerated. There were no serious adverse events. The vast majority over 90% ; of the adverse events that were experienced were rated as mild. Dose reductions were limited to one patient each in the 320 and 480 g dose cohorts with none in the 160 g dose cohort. No patients discontinued treatment. The majority of the side effects experienced by patients treated with Locteron in the SELECT-1 study in the 160, 320 and 480 g dose cohorts appear to be less frequent and less severe than the side effects reported in previous clinical trials for pegylated interferons and Albuferon. For example, only one patient in the SELECT-1 study receiving Locteron experienced an adverse event rated as severe, indicating an improvement over previously reported results in clinical trials for Pegasys and Albuferon as illustrated in Figure 1. more and aciphex.
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