Assessment of Sedative Activity of Lonicerin: In Vivo Approach With Pharmacokinetics and Molecular Docking

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Publicado en:Brain and Behavior vol. 15, no. 5 (May 1, 2025)
Autor principal: Eity, Tanzila Akter
Otros Autores: Bhuia, Md. Shimul, Chowdhury, Raihan, Sheikh, Salehin, Ansari, Siddique Akber, Ahammed, Nowreen Tabassum, Kamli, Hossam, Islam, Muhammad Torequl
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John Wiley & Sons, Inc.
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Acceso en línea:Citation/Abstract
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001 3210269073
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022 |a 2162-3279 
024 7 |a 10.1002/brb3.70524  |2 doi 
035 |a 3210269073 
045 0 |b d20250501 
084 |a 162435  |2 nlm 
100 1 |a Eity, Tanzila Akter  |u Department of Biotechnology and Genetic Engineering, Gopalganj Science and Technology University, Gopalganj, Bangladesh 
245 1 |a Assessment of Sedative Activity of Lonicerin: In Vivo Approach With Pharmacokinetics and Molecular Docking 
260 |b John Wiley & Sons, Inc.  |c May 1, 2025 
513 |a Journal Article 
520 3 |a ABSTRACT Background: Lonicerin (LON) has been identified to have different biological properties, such as anticancer, anti‐inflammatory, immunomodulatory, antibacterial, antimicrobial, and neuroprotective. This study aims to assess the sedative effect of LON in Swiss albino mice, which is yet to be discovered. Materials and Methods: Mice were treated with two different doses of LON (5 and 10 mg/kg) and 2 mg/kg of diazepam (DZP), which is the referral GABAergic medication, and the latency time and sleeping duration of animals were observed. A computational study was also conducted to evaluate the docking scores and display the binding sites of LON and receptor (GABAA α1 and β2 subunits). The study also investigated the pharmacokinetics and drug‐likeness properties of LON along with toxicological analysis by using SwissADME and Protox‐3 software, respectively. Results: Findings revealed that the higher concentration of LON reduced the latency (9.86 ± 1.44 min) and increased the sleep duration (191.29 ± 7.43 min) compared to the lower concentration. Besides, the combination group of LON and DZP showed the lowest latency (6.17 ± 0.82 min) and highest sleeping time (219.00 ± 6.39 min). In the in silico study, LON exhibited a strong docking score (−8.1 kcal/mol) with the macromolecules, which is closer to the binding affinity of DZP (–8.3 kcal/mol), indicating that LON could show strong sedative activity by binding with the GABAA receptor. Computational toxicity analysis revealed that LON is non‐hepatotoxic, non‐neurotoxic, noncarcinogenic, noncytotoxic, non‐ecotoxic, and non‐mutagenic. Conclusion: Therefore, LON may be effective for the treatment of insomnia in the near future. 
651 4 |a Bangladesh 
653 |a Insomnia 
653 |a Ligands 
653 |a Sleep 
653 |a Animals 
653 |a Albinism 
653 |a Natural products 
653 |a Energy consumption 
653 |a Benzodiazepines 
653 |a Drug dosages 
653 |a Variance analysis 
700 1 |a Bhuia, Md. Shimul  |u Department of Pharmacy, Gopalganj Science and Technology University, Gopalganj, Bangladesh 
700 1 |a Chowdhury, Raihan  |u Department of Pharmacy, Gopalganj Science and Technology University, Gopalganj, Bangladesh 
700 1 |a Sheikh, Salehin  |u Department of Pharmacy, Gopalganj Science and Technology University, Gopalganj, Bangladesh 
700 1 |a Ansari, Siddique Akber  |u Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia 
700 1 |a Ahammed, Nowreen Tabassum  |u Department of Biology, Touro University, New York City, New York, USA 
700 1 |a Kamli, Hossam  |u Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Khalid University, Abha, Saudi Arabia 
700 1 |a Islam, Muhammad Torequl  |u Department of Pharmacy, Gopalganj Science and Technology University, Gopalganj, Bangladesh 
773 0 |t Brain and Behavior  |g vol. 15, no. 5 (May 1, 2025) 
786 0 |d ProQuest  |t Health & Medical Collection 
856 4 1 |3 Citation/Abstract  |u https://www.proquest.com/docview/3210269073/abstract/embedded/J7RWLIQ9I3C9JK51?source=fedsrch 
856 4 0 |3 Full Text  |u https://www.proquest.com/docview/3210269073/fulltext/embedded/J7RWLIQ9I3C9JK51?source=fedsrch 
856 4 0 |3 Full Text - PDF  |u https://www.proquest.com/docview/3210269073/fulltextPDF/embedded/J7RWLIQ9I3C9JK51?source=fedsrch