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Neuropharmacological Assessment of the Hydroethanolic Leaf Extract of Calotropis procera (Ait). R. Br. (Apocynaceae) in Mice

BACKGROUND: Calotropis procera has been widely used traditionally for its analgesic and anti-inflammatory effects. It is also reportedly used in ethnomedicine for mental health disorders including epilepsy even in the absence of supporting scientific data. Thus, the potential of the plant to affect...

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Autores principales: Obese, Ernest, Ameyaw, Elvis Ofori, Biney, Robert Peter, Adakudugu, Emmanuel Awintiig, Woode, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270701/
https://www.ncbi.nlm.nih.gov/pubmed/34306795
http://dx.doi.org/10.1155/2021/5551380
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author Obese, Ernest
Ameyaw, Elvis Ofori
Biney, Robert Peter
Adakudugu, Emmanuel Awintiig
Woode, Eric
author_facet Obese, Ernest
Ameyaw, Elvis Ofori
Biney, Robert Peter
Adakudugu, Emmanuel Awintiig
Woode, Eric
author_sort Obese, Ernest
collection PubMed
description BACKGROUND: Calotropis procera has been widely used traditionally for its analgesic and anti-inflammatory effects. It is also reportedly used in ethnomedicine for mental health disorders including epilepsy even in the absence of supporting scientific data. Thus, the potential of the plant to affect neurological functions was evaluated. METHODS: Irwin's test was performed to determine the effect of the oral administration of the extract (30–3000 mg kg(−1)) on gross behaviour and physiological function. The activity meter, rotarod, pentylenetetrazol- (PTZ-) induced convulsion, pentobarbitone-induced sleep test, and the tail immersion tests were used to evaluate the spontaneous activity, neuromuscular function, convulsive threshold, sedation, and analgesic effects of the Calotropis procera extract (30–1000 mg/kg), respectively, in mice. RESULTS: Calotropis procera extract (CPE) exhibited significant (p < 0.0001) anticonvulsant and analgesic effects. There was a significant increase in withdrawal latency of the CPE-treated animals in the tail immersion test for analgesia (p < 0.0001), while latency and duration of PTZ-induced convulsions were positively modulated. Calotropis procera extract showed significant (p < 0.0001) central nervous system depressant effects in pentobarbitone-induced hypnosis at 100–1000 mg/kg and spontaneous activity test (30–1000 mg/kg). The extract also depicted impaired motor coordination at 100–1000 mg/kg dose levels. LD(50) was estimated to be above 1000 mg kg(−1). CONCLUSIONS: Calotropis procera extract has significant central nervous system depressant and analgesic effects in mice.
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spelling pubmed-82707012021-07-22 Neuropharmacological Assessment of the Hydroethanolic Leaf Extract of Calotropis procera (Ait). R. Br. (Apocynaceae) in Mice Obese, Ernest Ameyaw, Elvis Ofori Biney, Robert Peter Adakudugu, Emmanuel Awintiig Woode, Eric Scientifica (Cairo) Research Article BACKGROUND: Calotropis procera has been widely used traditionally for its analgesic and anti-inflammatory effects. It is also reportedly used in ethnomedicine for mental health disorders including epilepsy even in the absence of supporting scientific data. Thus, the potential of the plant to affect neurological functions was evaluated. METHODS: Irwin's test was performed to determine the effect of the oral administration of the extract (30–3000 mg kg(−1)) on gross behaviour and physiological function. The activity meter, rotarod, pentylenetetrazol- (PTZ-) induced convulsion, pentobarbitone-induced sleep test, and the tail immersion tests were used to evaluate the spontaneous activity, neuromuscular function, convulsive threshold, sedation, and analgesic effects of the Calotropis procera extract (30–1000 mg/kg), respectively, in mice. RESULTS: Calotropis procera extract (CPE) exhibited significant (p < 0.0001) anticonvulsant and analgesic effects. There was a significant increase in withdrawal latency of the CPE-treated animals in the tail immersion test for analgesia (p < 0.0001), while latency and duration of PTZ-induced convulsions were positively modulated. Calotropis procera extract showed significant (p < 0.0001) central nervous system depressant effects in pentobarbitone-induced hypnosis at 100–1000 mg/kg and spontaneous activity test (30–1000 mg/kg). The extract also depicted impaired motor coordination at 100–1000 mg/kg dose levels. LD(50) was estimated to be above 1000 mg kg(−1). CONCLUSIONS: Calotropis procera extract has significant central nervous system depressant and analgesic effects in mice. Hindawi 2021-07-01 /pmc/articles/PMC8270701/ /pubmed/34306795 http://dx.doi.org/10.1155/2021/5551380 Text en Copyright © 2021 Ernest Obese et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Obese, Ernest
Ameyaw, Elvis Ofori
Biney, Robert Peter
Adakudugu, Emmanuel Awintiig
Woode, Eric
Neuropharmacological Assessment of the Hydroethanolic Leaf Extract of Calotropis procera (Ait). R. Br. (Apocynaceae) in Mice
title Neuropharmacological Assessment of the Hydroethanolic Leaf Extract of Calotropis procera (Ait). R. Br. (Apocynaceae) in Mice
title_full Neuropharmacological Assessment of the Hydroethanolic Leaf Extract of Calotropis procera (Ait). R. Br. (Apocynaceae) in Mice
title_fullStr Neuropharmacological Assessment of the Hydroethanolic Leaf Extract of Calotropis procera (Ait). R. Br. (Apocynaceae) in Mice
title_full_unstemmed Neuropharmacological Assessment of the Hydroethanolic Leaf Extract of Calotropis procera (Ait). R. Br. (Apocynaceae) in Mice
title_short Neuropharmacological Assessment of the Hydroethanolic Leaf Extract of Calotropis procera (Ait). R. Br. (Apocynaceae) in Mice
title_sort neuropharmacological assessment of the hydroethanolic leaf extract of calotropis procera (ait). r. br. (apocynaceae) in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270701/
https://www.ncbi.nlm.nih.gov/pubmed/34306795
http://dx.doi.org/10.1155/2021/5551380
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