*P < 0 05, **P < 0 01 compared with that from mice in the control

Data were mean ± SD. *P < 0.05, **P < 0.01 compared with that from mice in the control group by one-way ANOVA test. Subacute toxicity evaluations Beginning on the third week of exposure to C-dots, the body weight of the rats in all groups selleck significantly increased (Table 4). The food intake and food utilization of the test groups were not significantly different between the negative groups (P > 0.05). Table 4 Diversification of rat body weight Gender Dose Number of rats Initial weight First week

(g) Second week (g) Third week (g) Fourth week       (g) F P       (g) F P Female Negative control 8 193.9 ± 8.24 0.327 Tozasertib molecular weight 0.806 204.5 ± 9.4 222.6 ± 11.6 237.4 ± 16.3 246.9 ± 18.8 0.177 0.911   Low 8 191.2 ± 7.70     201.8 ± 9.0 220.0 ± 12.1 237.4 ± 13.4 247.5 ± 12.4      

Middle 8 194.4 ± 7.01     203.4 ± 6.8 219.9 ± 11.0 234.8 ± 13.0 246.0 ± 14.3       High 8 194.6 ± 7.71     204.1 ± 10.4 220.2 ± 14.1 231.9 ± 18.7 241.9 ± 21.2     Male Negative control 8 207.9 ± 7.9 0.970 0.421 250.8 ± 9.6 308.4 ± 13.7 344.6 ± 18.4 383.8 ± 25.5 0.590 0.626   Low 8 210.2 ± 7.3     246.5 ± 7.7 302.1 ± 12.1 336.4 ± 7.7 373.0 ± 17.4       Middle 8 211.4 ± 8.8     245.9 ± 14.3 297.5 ± 16.8 336.0 ± 19.1 373.9 ± 26.2       High 8 205.0 ± 8.4     245.4 ± 11.4 308.5 ± 11.6 346.4 ± 15.6 383.6 ± 16.3     Body weight of rats was taken at different time points after C-dot treatment. Data were mean ± SD. Significant difference was Dichloromethane dehalogenase LY2603618 supplier analyzed by one-way ANOVA test. To reveal any potential toxic effect of the C-dots on the treated rats, biochemical and hematological analyses were performed. The following key hematology markers were assessed at various time points (1, 3, 7, and 28 days): white blood cells, red blood cells, platelets, lymphocytes, neutral cells, other cells, hemoglobin, and hematocrit (HCT) (Figure 2). All above

parameters in rats treated with different concentrations of C-dots at different time points appeared to be normal compared with the control groups. However, 7 days after exposure, the HCT of the low-dose C-dot-treated group showed a significant difference compared with that of the normal control group (P < 0.05). Figure 2 Blood hematology analysis of rats treated with C-dots. The rats were treated with C-dots at doses of 0.2, 2, and 20 mg/kg BW in 1, 3, 7 and 28 days. (A) White blood cells, (B) red blood cells, (C) hemoglobin, (D) HCT, (E) platelets, (F) lymphocytes, (G) neutral cells, and (H) other cells. Subacute C-dot poisoning can cause changes in the following biochemical indices: GOT, GPT, urea, Cr, cholesterol, TG, blood glucose, total protein, and albumin (Figure 3). On the first day after exposure, the blood arsenic level in the high-dose group was obviously higher than in the control group (P < 0.

Comments are closed.