Sedative effects of the naturally derived product NSDVT in experimental animals
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Tóm tắt
Sleep disturbance is a prominent and debilitating feature of chronic fatigue syndrome, underscoring the need for safe sedative agents. The present study investigated the sedative effects of NSDVT using standardized experimental models in mice. NSDVT was administered orally at 2.5 and 5 g/kg, with diazepam serving as a positive control. Spontaneous locomotor activity, Rotarod test, and hexobarbital-induced sleeping time were assessed. NSDVT significantly reduced both horizontal and vertical locomotor activity compared with baseline and control values. Diazepam produced a more pronounced reduction at 1 hour post-administration, whereas NSDVT, particularly at 5 g/kg, exhibited a stronger effect at 3 hours, indicating a delayed but sustained sedative action. In the rotarod test, both doses of NSDVT and diazepam significantly decreased the latency to fall. Similarly, diazepam exerted a greater effect at 1 hour, while NSDVT at 5 g/kg showed a more marked reduction at 3 hours. In the hexobarbital-induced sleep test, NSDVT did not affect sleep latency but significantly prolonged sleeping time to 113.45% and 150.83% of control values, with statistical significance observed at the higher dose. These findings demonstrate that NSDVT produces a clear sedative effect characterized by central nervous system depression with a delayed onset.
Chi tiết bài viết
Từ khóa
NSDVT, sedative, experimental animals, mice
Tài liệu tham khảo
2. Lim EJ, Ahn YC, Jang ES, et al. Systematic review and meta-analysis of the prevalence of chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME). J Transl Med. 2020; 18(1): 100. doi:10.1186/s12967-020-02269-0.
3. Liu T, Sun W, Guo S, et al. Research progress on pathogenesis of chronic fatigue syndrome and treatment of traditional Chinese and Western medicine. Auton Neurosci. 2024; 255: 103198. doi:10.1016/j.autneu.2024.103198.
4. Russell C, Kyle SD, Wearden AJ. Do evidence based interventions for chronic fatigue syndrome improve sleep? A systematic review and narrative synthesis. Sleep Med Rev. 2017; 33: 101-110. doi:10.1016/j.smrv.2016.05.001.
5. Zhang Y, Jin F, Wei X, et al. Chinese herbal medicine for the treatment of chronic fatigue syndrome: A systematic review and meta-analysis. Front Pharmacol. 2022; 13: 958005. doi:10.3389/fphar.2022.958005.
6. Lý Phi. Phương Tễ Học (quyển thượng). NXB Y tế cộng đồng; 2003.
7. Luo H, Sun SJ, Wang Y, Wang YL. Revealing the sedative-hypnotic effect of the extracts of herb pair Semen Ziziphi spinosae and Radix Polygalae and related mechanisms through experiments and metabolomics approach. BMC Complement Med Ther. 2020; 20(1): 206. doi:10.1186/s12906-020-03000-8.
8. Huang F, Xiong Y, Xu L, Ma S, Dou C. Sedative and hypnotic activities of the ethanol fraction from Fructus Schisandrae in mice and rats. J Ethnopharmacol. 2007;110(3):471-475. doi:10.1016/j.jep.2006.10.008.
9. Cục Khoa học công nghệ và đào tạo. Quyết định ban hành tài liệu chuyên môn “Hướng dẫn thử nghiệm tiền lâm sàng và lâm sàng thuốc đông y, thuốc từ dược liệu.” 2015.
10. Curzon P, Zhang M, Radek RJ, et al. The Behavioral Assessment of Sensorimotor Processes in the Mouse: Acoustic Startle, Sensory Gating, Locomotor Activity, Rotarod, and Beam Walking. In: Buccafusco JJ, ed. Methods of Behavior Analysis in Neuroscience. 2nd ed. Frontiers in Neuroscience. CRC Press/Taylor & Francis; 2009. Accessed December 22, 2025. http://www.ncbi.nlm.nih.gov/books/NBK5236/.
11. Komelkova M, Manukhina E, Downey HF, et al. Hexobarbital Sleep Test for Predicting the Susceptibility or Resistance to Experimental Posttraumatic Stress Disorder. Int J Mol Sci. 2020; 21(16): 5900. doi:10.3390/ijms21165900.
12. Jo K, Kim S, Ahn Y, et al. Effects of Green Lettuce Leaf Extract on Sleep Disturbance Control in Oxidative Stress-Induced Invertebrate and Vertebrate Models. Antioxidants. 2021; 10(6): 970. doi:10.3390/antiox10060970.
13. Majer M, Jones JF, Unger ER, et al. Perception versus polysomnographic assessment of sleep in CFS and non-fatigued control subjects: results from a population-based study. BMC Neurol. 2007; 7(1): 40. doi:10.1186/1471-2377-7-40.
14. Jackson ML, Bruck D. Sleep abnormalities in chronic fatigue syndrome/myalgic encephalomyelitis: a review. J Clin Sleep Med JCSM Off Publ Am Acad Sleep Med. 2012; 8(6): 719-728. doi:10.5664/jcsm.2276.
15. Umezu T. Evaluation of Central Nervous System Acting Effects of Plant-Derived Essential Oils Using Ambulatory Activity in Mice. Pharmacol Amp Pharm. 2013; 4(2): 160-170. doi:10.4236/pp.2013.42023.
16. Pádua-Reis M, Nôga DA, Tort ABL, et al. Diazepam causes sedative rather than anxiolytic effects in C57BL/6J mice. Sci Rep. 2021; 11(1): 9335. doi:10.1038/s41598-021-88599-5.
17. Dhaliwal JS, Rosani A, Saadabadi A. Diazepam. StatPearls. 2025.
18. Khonsary S. Goodman and Gilman’s The Pharmacological Basis of Therapeutics. Surg Neurol Int. 2023; 14: 91. doi:10.25259/SNI_184_2023.
19. Stanley JL, Lincoln RJ, Brown TA, et al. The mouse beam walking assay offers improved sensitivity over the mouse rotarod in determining motor coordination deficits induced by benzodiazepines. J Psychopharmacol Oxf Engl. 2005; 19(3): 221-227.
20. Skibiski J, Patel P, Abdijadid S. Barbiturates. StatPearls. 2025.
21. Knodell RG, Dubey RK, Wilkinson GR, Guengerich FP. Oxidative metabolism of hexobarbital in human liver: relationship to polymorphic S-mephenytoin 4-hydroxylation. J Pharmacol Exp Ther. 1988; 245(3): 845-849.