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Hypnotic, anticonvulsant and anxiolytic effects of 1-nitro-2-phenylethane isolated from the essential oil of Dennettia tripetala in mice.
Phytomedicine. 2013 Nov 15; 20(14):1315-22.P

Abstract

This study investigated the hypnotic, anti-convulsant and anxiolytic effects of 1-nitro-2-phenylethane (BPNE) obtained from the oil of Dennettia tripetala G. Baker (Annonaceae) and established its mechanism of action. The essential oil (EO) from the leaf, fruit and seed was obtained by hydrodistillation, followed by isolation of BPNE purified to 99.2% by accelerated gradient chromatography on silica, and identified by NMR and GC-MS. The pure BPNE and EO of the dried seed (93.6%) were comparatively evaluated for hypnotic, anticonvulsant and anxiolytic effects in mice. The acute toxicity of BPNE was determined and the LD50 was 490 mg/kg, intrapritonealy. The hypnotic activities of the EO and BPNE (50-400 mg/kg, i.p.) were assessed by loss of righting reflex, while sodium pentobarbitone (PBS) and diazepam (DZM) were used as positive controls. The anticonvulsant and anxiolytic effects of the EO and BPNE were evaluated in mice. Both BPNE and EO at doses ≥100 mg/kg induced spontaneous hypnosis with loss of righting reflex, significantly decreased sleep latency (SL) and also increased total sleeping time (TST) dose-dependently. They had comparable activity with NAP in TST. The BPNE exhibited higher hypnotic potency than EO at the same dose levels. The EO and BPNE offered comparable dose-related protections against PTZ- and strychnine-induced convulsions. Flumazenil (2 mg/kg) blocked the hypnotic and anticonvulsant (PTZ-convulsions) effects of both EO and BPNE. The essential oil at 5-20 mg/kg dose levels significantly (p<0.05) increased the percentage time spent and number of entries into the open arms. While at the same dose range BPNE significantly (p<0.05) increased the percentage time spent and the number of entries into the open arms respectively. The study concluded that 1-nitro-2-phenylethane exhibited dose dependent significant hypnotic, anticonvulsant and anxiolytic effects and it is the compound largely responsible for the neuropharmacological effects of the oil.

Authors+Show Affiliations

Department of Pharmacology, Obafemi Awolowo University, Ile-Ife, 220005 Osun State, Nigeria.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

23920280

Citation

Oyemitan, Idris Ajayi, et al. "Hypnotic, Anticonvulsant and Anxiolytic Effects of 1-nitro-2-phenylethane Isolated From the Essential Oil of Dennettia Tripetala in Mice." Phytomedicine : International Journal of Phytotherapy and Phytopharmacology, vol. 20, no. 14, 2013, pp. 1315-22.
Oyemitan IA, Elusiyan CA, Akanmu MA, et al. Hypnotic, anticonvulsant and anxiolytic effects of 1-nitro-2-phenylethane isolated from the essential oil of Dennettia tripetala in mice. Phytomedicine. 2013;20(14):1315-22.
Oyemitan, I. A., Elusiyan, C. A., Akanmu, M. A., & Olugbade, T. A. (2013). Hypnotic, anticonvulsant and anxiolytic effects of 1-nitro-2-phenylethane isolated from the essential oil of Dennettia tripetala in mice. Phytomedicine : International Journal of Phytotherapy and Phytopharmacology, 20(14), 1315-22. https://doi.org/10.1016/j.phymed.2013.07.005
Oyemitan IA, et al. Hypnotic, Anticonvulsant and Anxiolytic Effects of 1-nitro-2-phenylethane Isolated From the Essential Oil of Dennettia Tripetala in Mice. Phytomedicine. 2013 Nov 15;20(14):1315-22. PubMed PMID: 23920280.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Hypnotic, anticonvulsant and anxiolytic effects of 1-nitro-2-phenylethane isolated from the essential oil of Dennettia tripetala in mice. AU - Oyemitan,Idris Ajayi, AU - Elusiyan,Christianah Abimbola, AU - Akanmu,Moses Atanda, AU - Olugbade,Tiwalade Adewale, Y1 - 2013/08/03/ PY - 2013/04/29/received PY - 2013/06/24/revised PY - 2013/07/02/accepted PY - 2013/8/8/entrez PY - 2013/8/8/pubmed PY - 2014/5/9/medline KW - 1-Nitro-2-phenylethane KW - 1-nitro-2-phenylethane KW - AGC KW - Annonaceae KW - Anticonvulsant KW - Anxiolytic KW - BPNE KW - CNS KW - DZM KW - Dennettia tripetala KW - EO KW - FMZ KW - GABA KW - Hypnosis KW - IOAA KW - LRR KW - NAP KW - PTZ KW - SL KW - TLC KW - TST KW - VEH KW - accelerated gradient chromatography KW - central nervous system KW - diazepam KW - essential oil KW - flumazenil KW - gamma amino butyric acid KW - index of open arm avoidance KW - loss of righting reflex KW - pentylene tetrazole KW - sleep latency KW - sodium pentobarbitone KW - thin layer chromatography KW - total sleeping time KW - vehicle SP - 1315 EP - 22 JF - Phytomedicine : international journal of phytotherapy and phytopharmacology JO - Phytomedicine VL - 20 IS - 14 N2 - This study investigated the hypnotic, anti-convulsant and anxiolytic effects of 1-nitro-2-phenylethane (BPNE) obtained from the oil of Dennettia tripetala G. Baker (Annonaceae) and established its mechanism of action. The essential oil (EO) from the leaf, fruit and seed was obtained by hydrodistillation, followed by isolation of BPNE purified to 99.2% by accelerated gradient chromatography on silica, and identified by NMR and GC-MS. The pure BPNE and EO of the dried seed (93.6%) were comparatively evaluated for hypnotic, anticonvulsant and anxiolytic effects in mice. The acute toxicity of BPNE was determined and the LD50 was 490 mg/kg, intrapritonealy. The hypnotic activities of the EO and BPNE (50-400 mg/kg, i.p.) were assessed by loss of righting reflex, while sodium pentobarbitone (PBS) and diazepam (DZM) were used as positive controls. The anticonvulsant and anxiolytic effects of the EO and BPNE were evaluated in mice. Both BPNE and EO at doses ≥100 mg/kg induced spontaneous hypnosis with loss of righting reflex, significantly decreased sleep latency (SL) and also increased total sleeping time (TST) dose-dependently. They had comparable activity with NAP in TST. The BPNE exhibited higher hypnotic potency than EO at the same dose levels. The EO and BPNE offered comparable dose-related protections against PTZ- and strychnine-induced convulsions. Flumazenil (2 mg/kg) blocked the hypnotic and anticonvulsant (PTZ-convulsions) effects of both EO and BPNE. The essential oil at 5-20 mg/kg dose levels significantly (p<0.05) increased the percentage time spent and number of entries into the open arms. While at the same dose range BPNE significantly (p<0.05) increased the percentage time spent and the number of entries into the open arms respectively. The study concluded that 1-nitro-2-phenylethane exhibited dose dependent significant hypnotic, anticonvulsant and anxiolytic effects and it is the compound largely responsible for the neuropharmacological effects of the oil. SN - 1618-095X UR - https://www.unboundmedicine.com/medline/citation/23920280/Hypnotic_anticonvulsant_and_anxiolytic_effects_of_1_nitro_2_phenylethane_isolated_from_the_essential_oil_of_Dennettia_tripetala_in_mice_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0944-7113(13)00249-3 DB - PRIME DP - Unbound Medicine ER -