Literature DB >> 17971066

A novel cyclic squamosamide analogue compound FLZ improves memory impairment in artificial senescence mice induced by chronic injection of D-galactose and NaNO2.

Fang Fang1, Gengtao Liu.   

Abstract

The aim of the present study was to access the protective effect of a novel synthesized squamosamide cyclic analogue, compound FLZ, on memory impairment in artificially senescent mice induced by chronic injection of D-galactose and sodium nitrite (NaNO(2)). Artificially senescent mouse model was induced by consecutive injection of D-galactose (120 mg/kg) and NaNO(2) (90 mg/kg) once daily for 60 days. Compound FLZ (75 and 150 mg/kg) was orally administered once daily for 30 days after D-galactose and NaNO(2) injection for 30 days. The water maze test was used to evaluate the learning and memory function of mice. The content of malondialdehyde (MDA) and the activities of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) in serum were determined using different biochemical kits. The alterations in hippocampus morphology were assessed by light and electronic microscope. Immunoreactive cells of Bcl-2 in the hippocampus were counted by immunohistochemical staining, and Bcl-2 protein expression was analysed by Western blot method. The results indicate that injection of D-galactose and NaNO(2) induces memory impairment and neuronal damage in hippocampus of mice. In addition, serum SOD and GSH-Px activities decreased, while MDA level increased. Bcl-2-positive neurons and Bcl-2 protein expression in the hippocampus decreased remarkably. Oral administration of FLZ for 30 days significantly improved the cognitive deficits and the biochemical markers mentioned above, and also reduced the pathological alterations in mouse hippocampus. The results suggest that FLZ ameliorates memory deficits and pathological injury in artificially senescent mice induced by chronic injection of D-galactose and NaNO(2), indicating that FLZ is worth further studies for fighting antisenescence and dementia.

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Year:  2007        PMID: 17971066     DOI: 10.1111/j.1742-7843.2007.00138.x

Source DB:  PubMed          Journal:  Basic Clin Pharmacol Toxicol        ISSN: 1742-7835            Impact factor:   4.080


  9 in total

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3.  Ethanol extract of Scutellaria baicalensis Georgi prevents oxidative damage and neuroinflammation and memorial impairments in artificial senescense mice.

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Journal:  J Biomed Sci       Date:  2011-02-08       Impact factor: 8.410

4.  The novel squamosamide derivative FLZ enhances BDNF/TrkB/CREB signaling and inhibits neuronal apoptosis in APP/PS1 mice.

Authors:  Ning Li; Geng-tao Liu
Journal:  Acta Pharmacol Sin       Date:  2010-02-15       Impact factor: 6.150

5.  An in vivo microdialysis study of FLZ penetration through the blood-brain barrier in normal and 6-hydroxydopamine induced Parkinson's disease model rats.

Authors:  Jinfeng Hou; Qian Liu; Yingfei Li; Hua Sun; Jinlan Zhang
Journal:  Biomed Res Int       Date:  2014-06-23       Impact factor: 3.411

6.  Saffron (Crocus sativus L.) extract prevents and improves D-galactose and NaNO2 induced memory impairment in mice.

Authors:  M H Dashti-R; F Zeinali; M Anvari; S M Hosseini
Journal:  EXCLI J       Date:  2012-06-27       Impact factor: 4.068

7.  Rutin, a Flavonoid That Is a Main Component of Saussurea involucrata, Attenuates the Senescence Effect in D-Galactose Aging Mouse Model.

Authors:  Ying-Chen Yang; Hsueh-Yi Lin; Kang-Yi Su; Chien-Hsu Chen; Yung-Lung Yu; Chai-Ching Lin; Sung-Liang Yu; Hong-Young Yan; Kuo-Jung Su; Yi-Lin Sophia Chen
Journal:  Evid Based Complement Alternat Med       Date:  2012-08-16       Impact factor: 2.629

8.  Hippocampal neurochemical changes in senescent mice induced with chronic injection of D-galactose and NaNO₂: an in vitro high-resolution NMR spectroscopy study at 9.4T.

Authors:  Yan Lin; Jianli Yao; Yaowen Chen; Li Pang; Haihong Li; Zhen Cao; Kezeng You; Haiyang Dai; Renhua Wu
Journal:  PLoS One       Date:  2014-02-12       Impact factor: 3.240

9.  FLZ alleviates the memory deficits in transgenic mouse model of Alzheimer's disease via decreasing beta-amyloid production and tau hyperphosphorylation.

Authors:  Xiu-Qi Bao; Ning Li; Tao Wang; Xiang-Chen Kong; Wen-Jiao Tai; Hua Sun; Dan Zhang
Journal:  PLoS One       Date:  2013-11-04       Impact factor: 3.240

  9 in total

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