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Effects of a Proprietary Standardized Orthosiphon stamineus Ethanolic Leaf Extract on Enhancing Memory in Sprague Dawley Rats Possibly via Blockade of Adenosine A(2A) Receptors

The aim of the study was to explore a propriety standardized ethanolic extract from leaves of Orthosiphon stamineus Benth in improving impairments in short-term social memory in vivo, possibly via blockade of adenosine A(2A) receptors (A2AR). The ethanolic extract of O. stamineus leaves showed signi...

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Detalles Bibliográficos
Autores principales: George, Annie, Chinnappan, Sasikala, Choudhary, Yogendra, Choudhary, Vandana Kotak, Bommu, Praveen, Wong, Hoi Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655036/
https://www.ncbi.nlm.nih.gov/pubmed/26649059
http://dx.doi.org/10.1155/2015/375837
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author George, Annie
Chinnappan, Sasikala
Choudhary, Yogendra
Choudhary, Vandana Kotak
Bommu, Praveen
Wong, Hoi Jin
author_facet George, Annie
Chinnappan, Sasikala
Choudhary, Yogendra
Choudhary, Vandana Kotak
Bommu, Praveen
Wong, Hoi Jin
author_sort George, Annie
collection PubMed
description The aim of the study was to explore a propriety standardized ethanolic extract from leaves of Orthosiphon stamineus Benth in improving impairments in short-term social memory in vivo, possibly via blockade of adenosine A(2A) receptors (A2AR). The ethanolic extract of O. stamineus leaves showed significant in vitro binding activity of A2AR with 74% inhibition at 150 μg/ml and significant A2AR antagonist activity with 98% inhibition at 300 μg/mL. A significant adenosine A(1) receptor (A1R) antagonist activity with 100% inhibition was observed at 300 μg/mL. Its effect on learning and memory was assessed via social recognition task using Sprague Dawley rats whereby the ethanolic extract of O. stamineus showed significant (p < 0.001) change in recognition index (RI) at 300 mg/kg and 600 mg/kg p.o and 120 mg/kg i.p., respectively, compared to the vehicle control. In comparison, the ethanolic extract of Polygonum minus aerial parts showed small change in inflexion; however, it remained insignificant in RI at 200 mg/kg p.o. Our findings suggest that the ethanolic extract of O. stamineus leaves improves memory by reversing age-related deficits in short-term social memory and the possible involvement of adenosine A(1) and adenosine A(2A) as a target bioactivity site in the restoration of memory.
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spelling pubmed-46550362015-12-08 Effects of a Proprietary Standardized Orthosiphon stamineus Ethanolic Leaf Extract on Enhancing Memory in Sprague Dawley Rats Possibly via Blockade of Adenosine A(2A) Receptors George, Annie Chinnappan, Sasikala Choudhary, Yogendra Choudhary, Vandana Kotak Bommu, Praveen Wong, Hoi Jin Evid Based Complement Alternat Med Research Article The aim of the study was to explore a propriety standardized ethanolic extract from leaves of Orthosiphon stamineus Benth in improving impairments in short-term social memory in vivo, possibly via blockade of adenosine A(2A) receptors (A2AR). The ethanolic extract of O. stamineus leaves showed significant in vitro binding activity of A2AR with 74% inhibition at 150 μg/ml and significant A2AR antagonist activity with 98% inhibition at 300 μg/mL. A significant adenosine A(1) receptor (A1R) antagonist activity with 100% inhibition was observed at 300 μg/mL. Its effect on learning and memory was assessed via social recognition task using Sprague Dawley rats whereby the ethanolic extract of O. stamineus showed significant (p < 0.001) change in recognition index (RI) at 300 mg/kg and 600 mg/kg p.o and 120 mg/kg i.p., respectively, compared to the vehicle control. In comparison, the ethanolic extract of Polygonum minus aerial parts showed small change in inflexion; however, it remained insignificant in RI at 200 mg/kg p.o. Our findings suggest that the ethanolic extract of O. stamineus leaves improves memory by reversing age-related deficits in short-term social memory and the possible involvement of adenosine A(1) and adenosine A(2A) as a target bioactivity site in the restoration of memory. Hindawi Publishing Corporation 2015 2015-11-08 /pmc/articles/PMC4655036/ /pubmed/26649059 http://dx.doi.org/10.1155/2015/375837 Text en Copyright © 2015 Annie George et al. https://creativecommons.org/licenses/by/3.0/ 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
George, Annie
Chinnappan, Sasikala
Choudhary, Yogendra
Choudhary, Vandana Kotak
Bommu, Praveen
Wong, Hoi Jin
Effects of a Proprietary Standardized Orthosiphon stamineus Ethanolic Leaf Extract on Enhancing Memory in Sprague Dawley Rats Possibly via Blockade of Adenosine A(2A) Receptors
title Effects of a Proprietary Standardized Orthosiphon stamineus Ethanolic Leaf Extract on Enhancing Memory in Sprague Dawley Rats Possibly via Blockade of Adenosine A(2A) Receptors
title_full Effects of a Proprietary Standardized Orthosiphon stamineus Ethanolic Leaf Extract on Enhancing Memory in Sprague Dawley Rats Possibly via Blockade of Adenosine A(2A) Receptors
title_fullStr Effects of a Proprietary Standardized Orthosiphon stamineus Ethanolic Leaf Extract on Enhancing Memory in Sprague Dawley Rats Possibly via Blockade of Adenosine A(2A) Receptors
title_full_unstemmed Effects of a Proprietary Standardized Orthosiphon stamineus Ethanolic Leaf Extract on Enhancing Memory in Sprague Dawley Rats Possibly via Blockade of Adenosine A(2A) Receptors
title_short Effects of a Proprietary Standardized Orthosiphon stamineus Ethanolic Leaf Extract on Enhancing Memory in Sprague Dawley Rats Possibly via Blockade of Adenosine A(2A) Receptors
title_sort effects of a proprietary standardized orthosiphon stamineus ethanolic leaf extract on enhancing memory in sprague dawley rats possibly via blockade of adenosine a(2a) receptors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655036/
https://www.ncbi.nlm.nih.gov/pubmed/26649059
http://dx.doi.org/10.1155/2015/375837
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