author_facet Xu, Lin
Liu, Shao‐Lin
Zhang, Jun‐Tian
Xu, Lin
Liu, Shao‐Lin
Zhang, Jun‐Tian
author Xu, Lin
Liu, Shao‐Lin
Zhang, Jun‐Tian
spellingShingle Xu, Lin
Liu, Shao‐Lin
Zhang, Jun‐Tian
Chirality
(−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats
Organic Chemistry
Spectroscopy
Drug Discovery
Pharmacology
Catalysis
Analytical Chemistry
author_sort xu, lin
spelling Xu, Lin Liu, Shao‐Lin Zhang, Jun‐Tian 0899-0042 1520-636X Wiley Organic Chemistry Spectroscopy Drug Discovery Pharmacology Catalysis Analytical Chemistry http://dx.doi.org/10.1002/chir.20150 <jats:title>Abstract</jats:title><jats:p>The effect of clausenamide on synaptic transmission in the dentate gyrus of rats in vivo and its possible mechanism of action were investigated in this study. Four of 16 enantiomers showed potentiating effects on basal synaptic transmission in anesthetized animals. By comparing one pair of enantiomers, (−)‐clausenamide and (+)‐clausenamide, we can report three primary findings: (1) (−)‐clausenamide potentiated synaptic transmission in both anesthetized and freely moving animals while (+)‐clausenamide showed no or little effect; (2) (−)‐clausenamide increased the magnitude of long‐term potentiation (LTP) induced by high‐frequency stimulation (HFS) in anesthetized animals whereas (+)‐clausenamide had no effect; (3) voltage‐dependent calcium channels (VDCCs) calcineurin and calpain are involved in (−)‐clausenamide‐induced potentiation of synaptic transmission. Because hippocampal LTP is thought to reflect a cellular mechanism involved in learning and memory, our findings may provide the pharmacological basis for understanding the nootropic mechanisms of (−)‐clausenamide, which is the first chiral nootropic agent developed in China. <jats:italic>Chirality 17:239–244, 2005. </jats:italic>© 2005 Wiley‐Liss, Inc.</jats:p> (−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats Chirality
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title (−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats
title_unstemmed (−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats
title_full (−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats
title_fullStr (−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats
title_full_unstemmed (−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats
title_short (−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats
title_sort (−)‐clausenamide potentiates synaptic transmission in the dentate gyrus of rats
topic Organic Chemistry
Spectroscopy
Drug Discovery
Pharmacology
Catalysis
Analytical Chemistry
url http://dx.doi.org/10.1002/chir.20150
publishDate 2005
physical 239-244
description <jats:title>Abstract</jats:title><jats:p>The effect of clausenamide on synaptic transmission in the dentate gyrus of rats in vivo and its possible mechanism of action were investigated in this study. Four of 16 enantiomers showed potentiating effects on basal synaptic transmission in anesthetized animals. By comparing one pair of enantiomers, (−)‐clausenamide and (+)‐clausenamide, we can report three primary findings: (1) (−)‐clausenamide potentiated synaptic transmission in both anesthetized and freely moving animals while (+)‐clausenamide showed no or little effect; (2) (−)‐clausenamide increased the magnitude of long‐term potentiation (LTP) induced by high‐frequency stimulation (HFS) in anesthetized animals whereas (+)‐clausenamide had no effect; (3) voltage‐dependent calcium channels (VDCCs) calcineurin and calpain are involved in (−)‐clausenamide‐induced potentiation of synaptic transmission. Because hippocampal LTP is thought to reflect a cellular mechanism involved in learning and memory, our findings may provide the pharmacological basis for understanding the nootropic mechanisms of (−)‐clausenamide, which is the first chiral nootropic agent developed in China. <jats:italic>Chirality 17:239–244, 2005. </jats:italic>© 2005 Wiley‐Liss, Inc.</jats:p>
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author Xu, Lin, Liu, Shao‐Lin, Zhang, Jun‐Tian
author_facet Xu, Lin, Liu, Shao‐Lin, Zhang, Jun‐Tian, Xu, Lin, Liu, Shao‐Lin, Zhang, Jun‐Tian
author_sort xu, lin
container_issue 5
container_start_page 239
container_title Chirality
container_volume 17
description <jats:title>Abstract</jats:title><jats:p>The effect of clausenamide on synaptic transmission in the dentate gyrus of rats in vivo and its possible mechanism of action were investigated in this study. Four of 16 enantiomers showed potentiating effects on basal synaptic transmission in anesthetized animals. By comparing one pair of enantiomers, (−)‐clausenamide and (+)‐clausenamide, we can report three primary findings: (1) (−)‐clausenamide potentiated synaptic transmission in both anesthetized and freely moving animals while (+)‐clausenamide showed no or little effect; (2) (−)‐clausenamide increased the magnitude of long‐term potentiation (LTP) induced by high‐frequency stimulation (HFS) in anesthetized animals whereas (+)‐clausenamide had no effect; (3) voltage‐dependent calcium channels (VDCCs) calcineurin and calpain are involved in (−)‐clausenamide‐induced potentiation of synaptic transmission. Because hippocampal LTP is thought to reflect a cellular mechanism involved in learning and memory, our findings may provide the pharmacological basis for understanding the nootropic mechanisms of (−)‐clausenamide, which is the first chiral nootropic agent developed in China. <jats:italic>Chirality 17:239–244, 2005. </jats:italic>© 2005 Wiley‐Liss, Inc.</jats:p>
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spelling Xu, Lin Liu, Shao‐Lin Zhang, Jun‐Tian 0899-0042 1520-636X Wiley Organic Chemistry Spectroscopy Drug Discovery Pharmacology Catalysis Analytical Chemistry http://dx.doi.org/10.1002/chir.20150 <jats:title>Abstract</jats:title><jats:p>The effect of clausenamide on synaptic transmission in the dentate gyrus of rats in vivo and its possible mechanism of action were investigated in this study. Four of 16 enantiomers showed potentiating effects on basal synaptic transmission in anesthetized animals. By comparing one pair of enantiomers, (−)‐clausenamide and (+)‐clausenamide, we can report three primary findings: (1) (−)‐clausenamide potentiated synaptic transmission in both anesthetized and freely moving animals while (+)‐clausenamide showed no or little effect; (2) (−)‐clausenamide increased the magnitude of long‐term potentiation (LTP) induced by high‐frequency stimulation (HFS) in anesthetized animals whereas (+)‐clausenamide had no effect; (3) voltage‐dependent calcium channels (VDCCs) calcineurin and calpain are involved in (−)‐clausenamide‐induced potentiation of synaptic transmission. Because hippocampal LTP is thought to reflect a cellular mechanism involved in learning and memory, our findings may provide the pharmacological basis for understanding the nootropic mechanisms of (−)‐clausenamide, which is the first chiral nootropic agent developed in China. <jats:italic>Chirality 17:239–244, 2005. </jats:italic>© 2005 Wiley‐Liss, Inc.</jats:p> (−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats Chirality
spellingShingle Xu, Lin, Liu, Shao‐Lin, Zhang, Jun‐Tian, Chirality, (−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats, Organic Chemistry, Spectroscopy, Drug Discovery, Pharmacology, Catalysis, Analytical Chemistry
title (−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats
title_full (−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats
title_fullStr (−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats
title_full_unstemmed (−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats
title_short (−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats
title_sort (−)‐clausenamide potentiates synaptic transmission in the dentate gyrus of rats
title_unstemmed (−)‐Clausenamide potentiates synaptic transmission in the dentate gyrus of rats
topic Organic Chemistry, Spectroscopy, Drug Discovery, Pharmacology, Catalysis, Analytical Chemistry
url http://dx.doi.org/10.1002/chir.20150