Quercetin increases the antidepressant-like effects of sclareol and antagonizes diazepam in thiopental sodium-induced sleeping mice: A possible GABAergic transmission intervention

被引:10
|
作者
Bappi, Mehedi Hasan [1 ]
Mia, Md. Nayem [1 ]
Ansari, Siddique Akber [2 ]
Ansari, Irfan Aamer [3 ]
Prottay, Abdullah Al Shamsh [1 ]
Akbor, Md. Showkoth [1 ]
El-Nashar, Heba A. S. [4 ,6 ]
El-Shazly, Mohamed [4 ,6 ]
Mubarak, Mohammad S. [5 ]
Torequl Islam, Muhammad [1 ,7 ]
机构
[1] Bangabandhu Sheikh Mujibur Rahman Sci & Technol Un, Dept Pharm, Gopalganj 8100, Bangladesh
[2] King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, Riyadh, Saudi Arabia
[3] Univ Turin, Dept Drug Sci & Technol, Turin, Italy
[4] Ain Shams Univ, Fac Pharm, Dept Pharmacognosy, Cairo, Egypt
[5] Univ Jordan, Dept Chem, Amman, Jordan
[6] Ain Shams Univ, Fac Pharm, Dept Pharmacognosy, Cairo 11566, Egypt
[7] Bangabandhu Sheikh Mujibur Rahman Sci & Technol Un, Dept Pharm, Gopalganj 8100, Bangladesh
关键词
combined treatment strategy; computer-assisted studies; depression; quercetin; sclareol; IN-VIVO; SEX-DIFFERENCES; ANIMAL-MODELS; ANXIETY; DEPRESSION; NEURONS; ALPHA; GABA; SIMULATIONS; INDUCTION;
D O I
10.1002/ptr.8139
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Quercetin is the most common polyphenolic flavonoid present in fruits and vegetables demonstrating versatile health-promoting effects. This study aimed to examine the effects of quercetin (QR) and sclareol (SCL) on the thiopental sodium (TS)-induced sleeping and forced swimming test (FST) mouse models. SCL (1, 5, and 10 mg/kg, p.o.) or QR (50 mg/kg, p.o.) and/or diazepam (DZP) (3 mg/kg, i.p.) were employed. After 30 min of TS induction, individual or combined effects on the animals were checked. In the FST test, the animals were subjected to forced swimming after 30 min of administration of the test and/or controls for 5 min. In this case, immobility time was measured. In silico studies were conducted to evaluate the involvement of GABA receptors. SCL (5 and 10 mg/kg) significantly increased the latency and decreased sleeping time compared to the control in the TS-induced sleeping time study. DZP (3 mg/kg) showed a sedative-like effect in animals in both sleeping and FST studies. QR (50 mg/kg) exhibited a similar pattern of activity as SCL. However, its effects were more prominent than those of SCL groups. SCL (10 mg/kg) altered the DZP-3-mediated effects. SCL-10 co-treated with QR-50 significantly (p < 0.05) increased the latency and decreased sleep time and immobility time, suggesting possible synergistic antidepressant-like effects. In silico studies revealed that SCL and QR demonstrated better binding affinities with GABAA receptor, especially alpha 2, alpha 3, and alpha 5 subunits. Both compounds also exhibited good ADMET and drug-like properties. In animal studies, the both compounds worked synergistically to provide antidepressant-like effects in a slightly different fashion. As a conclusion, the combined administration of SCL and QR may be used in upcoming neurological clinical trials, according to in vivo and in silico findings. However, additional investigation is necessary to verify this behavior and clarify the potential mechanism of action.
引用
收藏
页码:2198 / 2214
页数:17
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