2007
DOI: 10.1016/j.neuropharm.2007.02.008
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Dehydroevodiamine attenuates tau hyperphosphorylation and spatial memory deficit induced by activation of glycogen synthase kinase-3 in rats

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Cited by 41 publications
(35 citation statements)
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“…Many sites of tau phosphorylation are serine or threonine residues that are immediately followed in the sequence by Proline residues, and hence are candidate phosphorylation sites for Proline-directed kinases [129,130]. GSK-3 plays a central role in AD, which is involved in the hyperphosphorylation of tau [131,132] Fig.…”
Section: Gsk-3 Directly Phosphorylates Taumentioning
confidence: 99%
“…Many sites of tau phosphorylation are serine or threonine residues that are immediately followed in the sequence by Proline residues, and hence are candidate phosphorylation sites for Proline-directed kinases [129,130]. GSK-3 plays a central role in AD, which is involved in the hyperphosphorylation of tau [131,132] Fig.…”
Section: Gsk-3 Directly Phosphorylates Taumentioning
confidence: 99%
“…Our study reported that DeHE pretreatment attenuated intracerebroventricular administration of beta-amyloid peptide (25-35) and intraperitoneal administration of scopolamine induced amnesia in mice [62]. Furthermore, pre-administration of DeHE via vena caudalis for one week effectively improved the Wortmannin and GF-109 203X (WT/GFX) induced spatial memory retention impairment of rats, antagonized tau hyperphosphorylation at multiple Alzheimer's disease site and arrested the overactivation of glycogen synthase kinase-3 induced by WT/GFX [63]. DeHE did not cause any serious adverse effects at the dose levels in the experimental animals [64].…”
Section: Introductionmentioning
confidence: 99%
“…It could also protect against learning and memory impairment in both scopolamine-and Ab-induced amnesia animal. The mechanism of the neuroprotective effects of dehyroevodiamine has been examined by Peng et al [17,18].…”
Section: Resultsmentioning
confidence: 99%