Tabernaemontana divaricata extract inhibits neuronal acetylcholinesterase activity in rats
The current pharmacotherapy for Alzheimer's disease (AD) is the use of acetylcholinesterase inhibitors (AChE-Is). A previous in vitro study showed that Tabernaemontana divaricata extract (TDE) can inhibit AChE activity. However, neither the AChE inhibitory effects nor the effect on neuronal act...
Saved in:
Main Authors: | , , , , , |
---|---|
Format: | Journal |
Published: |
2018
|
Subjects: | |
Online Access: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33846827338&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/61382 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Chiang Mai University |
id |
th-cmuir.6653943832-61382 |
---|---|
record_format |
dspace |
spelling |
th-cmuir.6653943832-613822018-09-10T04:09:47Z Tabernaemontana divaricata extract inhibits neuronal acetylcholinesterase activity in rats Siriporn Chattipakorn Anucha Pongpanparadorn Wasana Pratchayasakul Anchalee Pongchaidacha Kornkanok Ingkaninan Nipon Chattipakorn Pharmacology, Toxicology and Pharmaceutics The current pharmacotherapy for Alzheimer's disease (AD) is the use of acetylcholinesterase inhibitors (AChE-Is). A previous in vitro study showed that Tabernaemontana divaricata extract (TDE) can inhibit AChE activity. However, neither the AChE inhibitory effects nor the effect on neuronal activity of TDE has been investigated in vivo. To determine those effects of TDE in animal models, the Ellman's colorimetric method was implemented to investigate the cortical and circulating cholinesterase (ChE) activity, and Fos expression was used to determine the neuronal activity in the cerebral cortex, following acute administration of TDE with various doses (250, 500 and 1000 mg/kg) and at different time points. All doses of TDE 2 h after a single administration significantly inhibited cortical AChE activity and enhanced neuronal activity in the cerebral cortex. The enhancement of Fos expression and AChE inhibitory effects in the cerebral cortex among the three TDE-treated groups was not significantly different. A 2 h interval following all doses of TDE administration had no effect on circulating ChE activity. However, TDE significantly inhibited circulating AChE 10, 30 and 60 min after administration. Our findings suggest that TDE is a reversible AChE-I and could be beneficial as a novel therapeutic agent for AD. © 2006 Elsevier Ireland Ltd. All rights reserved. 2018-09-10T04:09:47Z 2018-09-10T04:09:47Z 2007-03-01 Journal 03788741 2-s2.0-33846827338 10.1016/j.jep.2006.09.007 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33846827338&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/61382 |
institution |
Chiang Mai University |
building |
Chiang Mai University Library |
country |
Thailand |
collection |
CMU Intellectual Repository |
topic |
Pharmacology, Toxicology and Pharmaceutics |
spellingShingle |
Pharmacology, Toxicology and Pharmaceutics Siriporn Chattipakorn Anucha Pongpanparadorn Wasana Pratchayasakul Anchalee Pongchaidacha Kornkanok Ingkaninan Nipon Chattipakorn Tabernaemontana divaricata extract inhibits neuronal acetylcholinesterase activity in rats |
description |
The current pharmacotherapy for Alzheimer's disease (AD) is the use of acetylcholinesterase inhibitors (AChE-Is). A previous in vitro study showed that Tabernaemontana divaricata extract (TDE) can inhibit AChE activity. However, neither the AChE inhibitory effects nor the effect on neuronal activity of TDE has been investigated in vivo. To determine those effects of TDE in animal models, the Ellman's colorimetric method was implemented to investigate the cortical and circulating cholinesterase (ChE) activity, and Fos expression was used to determine the neuronal activity in the cerebral cortex, following acute administration of TDE with various doses (250, 500 and 1000 mg/kg) and at different time points. All doses of TDE 2 h after a single administration significantly inhibited cortical AChE activity and enhanced neuronal activity in the cerebral cortex. The enhancement of Fos expression and AChE inhibitory effects in the cerebral cortex among the three TDE-treated groups was not significantly different. A 2 h interval following all doses of TDE administration had no effect on circulating ChE activity. However, TDE significantly inhibited circulating AChE 10, 30 and 60 min after administration. Our findings suggest that TDE is a reversible AChE-I and could be beneficial as a novel therapeutic agent for AD. © 2006 Elsevier Ireland Ltd. All rights reserved. |
format |
Journal |
author |
Siriporn Chattipakorn Anucha Pongpanparadorn Wasana Pratchayasakul Anchalee Pongchaidacha Kornkanok Ingkaninan Nipon Chattipakorn |
author_facet |
Siriporn Chattipakorn Anucha Pongpanparadorn Wasana Pratchayasakul Anchalee Pongchaidacha Kornkanok Ingkaninan Nipon Chattipakorn |
author_sort |
Siriporn Chattipakorn |
title |
Tabernaemontana divaricata extract inhibits neuronal acetylcholinesterase activity in rats |
title_short |
Tabernaemontana divaricata extract inhibits neuronal acetylcholinesterase activity in rats |
title_full |
Tabernaemontana divaricata extract inhibits neuronal acetylcholinesterase activity in rats |
title_fullStr |
Tabernaemontana divaricata extract inhibits neuronal acetylcholinesterase activity in rats |
title_full_unstemmed |
Tabernaemontana divaricata extract inhibits neuronal acetylcholinesterase activity in rats |
title_sort |
tabernaemontana divaricata extract inhibits neuronal acetylcholinesterase activity in rats |
publishDate |
2018 |
url |
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33846827338&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/61382 |
_version_ |
1681425610199531520 |