Verma Krishan K, Singh Umesh K, Jain Jainendra
Department of Pharmacy, Ram-Eesh Institute of Vocational & Technical Education, Plot No. 3, Knowledge Park-I, Greater Noida, UP, India.
Kherwal Department of Pharmacy, Swami Vivekanand Subharti University, Meerut Bypass, Meerut, UP, India.
Cent Nerv Syst Agents Med Chem. 2020;20(1):41-48. doi: 10.2174/1871524919666191209103003.
In the present study, we synthesized fifteen 4, 5-disubstituted 1, 2, 4-triazol- 3-thione derivatives and evaluated for anticonvulsant activity with neurotoxicity determination.
The synthesized compounds were characterized using FTIR, 1H-NMR and MS. The molecular docking study was also performed to study the interactions of compounds with LYS329 residue of gamma amino butyric acid aminotransferase (GABA-AT) using Autodock 4.2 software. The anticonvulsant activity was assessed by maximal electroshock (MES) test and subcutaneous pentylenetetrazol (scPTZ) tests. The neurotoxicity was assessed by rotarod ataxia test.
In MES test, compounds 5a, 8a and 9a were found active at 100 mg/kg and five compounds were found active at 300 mg/kg dose after 1 hr of administration. After 4 hr of drug administration, only two compounds 8a and 9a exhibited protection at 100 mg/kg. In scPTZ test, three compounds 2a, 6a and 8a were found active at 100 mg/kg and 7a was active at 300 mg/kg after 1 hr of test drug administration. Most of the compounds were found active in MES test with 8a and 9a being the most active among all. In docking study, 2a was found to be best compound based on the binding energy of -6.5 kcal/mol and estimated inhibition constant of 17.2 µM.
Majority of synthesized compounds were found active in MES test, whereas only few were found to possess anti scPTZ activity. Among all compounds, only 14a caused motor coordination impairment in rotarod ataxia test at 300 mg/kg 1 hr duration.
在本研究中,我们合成了15种4,5-二取代的1,2,4-三唑-3-硫酮衍生物,并对其进行抗惊厥活性评估及神经毒性测定。
利用傅里叶变换红外光谱(FTIR)、核磁共振氢谱(1H-NMR)和质谱(MS)对合成的化合物进行表征。还使用Autodock 4.2软件进行分子对接研究,以研究化合物与γ-氨基丁酸转氨酶(GABA-AT)的LYS329残基的相互作用。通过最大电休克(MES)试验和皮下注射戊四氮(scPTZ)试验评估抗惊厥活性。通过转棒共济失调试验评估神经毒性。
在MES试验中,化合物5a、8a和9a在给药1小时后,在100 mg/kg剂量下表现出活性,5种化合物在300 mg/kg剂量下表现出活性。给药4小时后,只有两种化合物8a和9a在100 mg/kg剂量下表现出保护作用。在scPTZ试验中,给药1小时后,3种化合物2a、6a和8a在100 mg/kg剂量下表现出活性,7a在300 mg/kg剂量下表现出活性。大多数化合物在MES试验中表现出活性,其中8a和9a是所有化合物中活性最高的。在对接研究中,基于-6.5 kcal/mol的结合能和17.2 µM的估计抑制常数,发现2a是最佳化合物。
大多数合成化合物在MES试验中表现出活性,而只有少数具有抗scPTZ活性。在所有化合物中,只有14a在300 mg/kg、持续1小时的转棒共济失调试验中导致运动协调障碍。