Department of Pharmacology and Toxicology, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran.
Isfahan Pharmaceutical Sciences Research Center, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran.
Neurotoxicol Teratol. 2021 Mar-Apr;84:106957. doi: 10.1016/j.ntt.2021.106957. Epub 2021 Feb 1.
Phosalone (Pln) is an organophosphorus pesticide acetylcholinesterase (AChE) inhibitor. Blockade of AChE amplifies ACh signaling that is related to depressive symptoms. The effects of Pln exposure were evaluated on depressive behavior in mice and the involvement of muscarinic ACh receptor (MAChR) was assessed.
After measuring total activity in the locomotor test the immobility time during the forced swimming test (FST) in male mice was evaluated as an index of depression. Pln single dose was administered by gavage feeding and examined after 3 h (day1) and on day 7 for evaluating delayed toxicity. In separate groups Pln was administered for 5 consecutive days and examined on day 6 also after one-week delay on day12.
While there were only marginal differences in the locomotor tests. Immobility time during the FST significantly increased on day1 by Pln 6, 12, 40 mg/kg (185 ± 17 s, 186 ± 9 s, 172.0 ± 7 s respectively) compared with control animals (149 ± 8 s, p < 0.01), immobility time was higher than control on day 6 after multiple exposures to Pln (0.6, 6, 12, 20 mg/kg 190 ± 20s, 210 ± 4 s, 196 ± 10s, 204 ± 9 respectively, vs control 153 ± 7 p < 0.001). The immobility time remained high following a week of relapse. The co-administration of Pln with scopolamine (Scp) a MAChR antagonist reduced immobility time (141 ± 10s vs Pln 186 ± 9 s, p < 0.01).
Single exposure to Pln induced depressive-like effects that were reversed by Scp, indicating that MAChR stimulation may be involved. While cumulative exposures caused more pronounced changes in depressive behavior that remained after a week from the last exposure.
磷硫磷(Pln)是一种有机磷农药乙酰胆碱酯酶(AChE)抑制剂。AChE 的阻断会放大与抑郁症状相关的 ACh 信号。评估了 Pln 暴露对小鼠抑郁行为的影响,并评估了毒蕈碱型乙酰胆碱受体(MAChR)的参与情况。
在测量了雄性小鼠的运动试验中的总活性后,通过强迫游泳试验(FST)中的不动时间评估作为抑郁的指标。Pln 通过灌胃给药给予单剂量,并在 3 小时后(第 1 天)和第 7 天进行检查,以评估迟发性毒性。在单独的组中,Pln 连续 5 天给药,并在第 6 天进行检查,在第 1 天延迟一周后在第 12 天也进行检查。
虽然在运动试验中只有微小的差异,但 Pln 6、12、40mg/kg(185±17s、186±9s、172.0±7s)在第 1 天的 FST 中的不动时间明显增加与对照动物(149±8s,p<0.01)相比,在多次接触 Pln 后,第 6 天的不动时间高于对照(0.6、6、12、20mg/kg 190±20s、210±4s、196±10s、204±9s,与对照 153±7p<0.001)。在一周的复发后,不动时间仍然很高。Pln 与 scopolamine(Scp)的共同给药,一种 MAChR 拮抗剂,减少了不动时间(141±10s 与 Pln 186±9s,p<0.01)。
单次接触 Pln 诱导了类似抑郁的影响,这些影响被 Scp 逆转,表明 MAChR 刺激可能参与其中。虽然累积暴露导致抑郁行为的更明显变化,这些变化在最后一次暴露一周后仍然存在。