Cargando…

Krill-Derived Phosphatidylserine Improves TMT-Induced Memory Impairment in the Rat

The present study examined the effects of krill-derived phosphatidylserine (Krill-PS) on the learning and memory function and the neural activity in rats with trimethyltin (TMT)-induced memory deficits. The rats were administered vehicle (medium-chain triglyceride: MCT) or Krill-PS (50, 100 mg/kg, p...

Descripción completa

Detalles Bibliográficos
Autores principales: Shim, Hyun Soo, Park, Hyun-Jung, Ahn, Yong Ho, Her, Song, Han, Jeong-Jun, Hahm, Dae-Hyun, Lee, Hyejung, Shim, Insop
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Applied Pharmacology 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3792220/
https://www.ncbi.nlm.nih.gov/pubmed/24116297
http://dx.doi.org/10.4062/biomolther.2012.20.2.207
_version_ 1782286831615737856
author Shim, Hyun Soo
Park, Hyun-Jung
Ahn, Yong Ho
Her, Song
Han, Jeong-Jun
Hahm, Dae-Hyun
Lee, Hyejung
Shim, Insop
author_facet Shim, Hyun Soo
Park, Hyun-Jung
Ahn, Yong Ho
Her, Song
Han, Jeong-Jun
Hahm, Dae-Hyun
Lee, Hyejung
Shim, Insop
author_sort Shim, Hyun Soo
collection PubMed
description The present study examined the effects of krill-derived phosphatidylserine (Krill-PS) on the learning and memory function and the neural activity in rats with trimethyltin (TMT)-induced memory deficits. The rats were administered vehicle (medium-chain triglyceride: MCT) or Krill-PS (50, 100 mg/kg, p.o.) daily for 21 days. The cognitive improving efficacy of Krill-PS in TMT-induced amnesic rats was investigated by assessing the Morris water maze test and by performing choline acetyltransferase (ChAT), acetylcholinesterase (AChE) and cAMP responsive element binding protein (CREB) immunohistochemistry. The rats with TMT injection showed impaired learning and memory of the tasks and treatment with Krill-PS produced a significant improvement of the escape latency to find the platform in the Morris water maze at the 2(nd) and 4(th) day compared to that of the MCT group (p<0.05). In the retention test, the Krill-PS+MCT groups showed increased time spent around the platform compared to that of the MCT group. Consistent with the behavioral data, Krill-PS 50+MCT group significantly alleviated the loss of acetylcholinergic neurons in the hippocampus and medial septum compared to that of the MCT group. Treatment with Krill-PS significantly increased the CREB positive neurons in the hippocampal CA1 area as compared to that of the MCT group. These results suggest that Krill-PS may be useful for improving the cognitive function via regulation of cholinergic marker enzyme activity and neural activity.
format Online
Article
Text
id pubmed-3792220
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher The Korean Society of Applied Pharmacology
record_format MEDLINE/PubMed
spelling pubmed-37922202013-10-10 Krill-Derived Phosphatidylserine Improves TMT-Induced Memory Impairment in the Rat Shim, Hyun Soo Park, Hyun-Jung Ahn, Yong Ho Her, Song Han, Jeong-Jun Hahm, Dae-Hyun Lee, Hyejung Shim, Insop Biomol Ther (Seoul) Articles The present study examined the effects of krill-derived phosphatidylserine (Krill-PS) on the learning and memory function and the neural activity in rats with trimethyltin (TMT)-induced memory deficits. The rats were administered vehicle (medium-chain triglyceride: MCT) or Krill-PS (50, 100 mg/kg, p.o.) daily for 21 days. The cognitive improving efficacy of Krill-PS in TMT-induced amnesic rats was investigated by assessing the Morris water maze test and by performing choline acetyltransferase (ChAT), acetylcholinesterase (AChE) and cAMP responsive element binding protein (CREB) immunohistochemistry. The rats with TMT injection showed impaired learning and memory of the tasks and treatment with Krill-PS produced a significant improvement of the escape latency to find the platform in the Morris water maze at the 2(nd) and 4(th) day compared to that of the MCT group (p<0.05). In the retention test, the Krill-PS+MCT groups showed increased time spent around the platform compared to that of the MCT group. Consistent with the behavioral data, Krill-PS 50+MCT group significantly alleviated the loss of acetylcholinergic neurons in the hippocampus and medial septum compared to that of the MCT group. Treatment with Krill-PS significantly increased the CREB positive neurons in the hippocampal CA1 area as compared to that of the MCT group. These results suggest that Krill-PS may be useful for improving the cognitive function via regulation of cholinergic marker enzyme activity and neural activity. The Korean Society of Applied Pharmacology 2012-03 /pmc/articles/PMC3792220/ /pubmed/24116297 http://dx.doi.org/10.4062/biomolther.2012.20.2.207 Text en Copyright ©2012, The Korean Society of Applied Pharmacology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Shim, Hyun Soo
Park, Hyun-Jung
Ahn, Yong Ho
Her, Song
Han, Jeong-Jun
Hahm, Dae-Hyun
Lee, Hyejung
Shim, Insop
Krill-Derived Phosphatidylserine Improves TMT-Induced Memory Impairment in the Rat
title Krill-Derived Phosphatidylserine Improves TMT-Induced Memory Impairment in the Rat
title_full Krill-Derived Phosphatidylserine Improves TMT-Induced Memory Impairment in the Rat
title_fullStr Krill-Derived Phosphatidylserine Improves TMT-Induced Memory Impairment in the Rat
title_full_unstemmed Krill-Derived Phosphatidylserine Improves TMT-Induced Memory Impairment in the Rat
title_short Krill-Derived Phosphatidylserine Improves TMT-Induced Memory Impairment in the Rat
title_sort krill-derived phosphatidylserine improves tmt-induced memory impairment in the rat
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3792220/
https://www.ncbi.nlm.nih.gov/pubmed/24116297
http://dx.doi.org/10.4062/biomolther.2012.20.2.207
work_keys_str_mv AT shimhyunsoo krillderivedphosphatidylserineimprovestmtinducedmemoryimpairmentintherat
AT parkhyunjung krillderivedphosphatidylserineimprovestmtinducedmemoryimpairmentintherat
AT ahnyongho krillderivedphosphatidylserineimprovestmtinducedmemoryimpairmentintherat
AT hersong krillderivedphosphatidylserineimprovestmtinducedmemoryimpairmentintherat
AT hanjeongjun krillderivedphosphatidylserineimprovestmtinducedmemoryimpairmentintherat
AT hahmdaehyun krillderivedphosphatidylserineimprovestmtinducedmemoryimpairmentintherat
AT leehyejung krillderivedphosphatidylserineimprovestmtinducedmemoryimpairmentintherat
AT shiminsop krillderivedphosphatidylserineimprovestmtinducedmemoryimpairmentintherat