Literature DB >> 1615059

Senescence-accelerated mouse (SAM): age-related reduced anxiety-like behavior in the SAM-P/8 strain.

M Miyamoto1, Y Kiyota, M Nishiyama, A Nagaoka.   

Abstract

Age-related behavioral changes in the passive avoidance, food neophobia, elevated plus-maze, and water-lick conflict tests were studied using substrains of senescence-accelerated mouse (SAM-P/8 and SAM-R/1) at 2 to 20 months of age. SAM-P/8 mice exhibited a significant impairment of acquisition of passive avoidance compared with SAM-R/1 mice when they were trained repeatedly, and the acquired response in SAM-P/8 mice rapidly diminished in contrast to good retention in SAM-R/1 mice. SAM-P/8 mice showed an age-related decrease in the latency to eat novel food after a 24-h food deprivation as compared with SAM-R/1 mice at 2 to 12 months of age, despite no significant difference in latency to eat familiar food between the two strains. In the elevated plus-maze test, SAM-P/8 mice had apparent increases in the number of entries into open arms and time spent on open arms in comparison to SAM-R/1 mice at 4 through 12 months of age; this difference became obvious with aging, implying age-associated reduced anxiety in the SAM-P/8 strain. In addition, SAM-P/8 mice exhibited a significant increase in punished water drinking compared to SAM-R/1 mice in the water-lick conflict test, although unpunished water intake in SAM-P/8 mice did not differ from that in the SAM-R/1 control. Aged SAM-R/1 mice, 20 months old, exhibited low anxiety-like behavior in the food neophobia and elevated plus-maze tests such as was seen in SAM-P/8 mice, when compared with young (4-month-old) SAM-R/1 mice.(ABSTRACT TRUNCATED AT 250 WORDS)

Entities:  

Mesh:

Year:  1992        PMID: 1615059     DOI: 10.1016/0031-9384(92)90081-c

Source DB:  PubMed          Journal:  Physiol Behav        ISSN: 0031-9384


  16 in total

1.  Amyloid and tau pathology of familial Alzheimer's disease APP/PS1 mouse model in a senescence phenotype background (SAMP8).

Authors:  D Porquet; P Andrés-Benito; C Griñán-Ferré; A Camins; I Ferrer; A M Canudas; J Del Valle; Mercè Pallàs
Journal:  Age (Dordr)       Date:  2015-02-08

2.  The aging brain: is function dependent on growth hormone/insulin-like growth factor-1 signaling?

Authors:  B A Forshee
Journal:  Age (Dordr)       Date:  2006-06-03

3.  Chronic adjunction of 1-deoxynojirimycin protects from age-related behavioral and biochemical changes in the SAMP8 mice.

Authors:  Gui-Hai Chen; Jing-Jing Tong; Fang Wang; Xue-Qin Hu; Xue-Wei Li; Fei Tao; Zhao-Jun Wei
Journal:  Age (Dordr)       Date:  2015-09-23

4.  Dietary resveratrol prevents Alzheimer's markers and increases life span in SAMP8.

Authors:  David Porquet; Gemma Casadesús; Sergi Bayod; Alberto Vicente; Anna M Canudas; Jordi Vilaplana; Carme Pelegrí; Coral Sanfeliu; Antoni Camins; Mercè Pallàs; Jaume del Valle
Journal:  Age (Dordr)       Date:  2012-11-07

Review 5.  Senescence-accelerated mouse (SAM) with special references to neurodegeneration models, SAMP8 and SAMP10 mice.

Authors:  Toshio Takeda
Journal:  Neurochem Res       Date:  2009-02-07       Impact factor: 3.996

6.  Dietary Protein Source Influences Brain Inflammation and Memory in a Male Senescence-Accelerated Mouse Model of Dementia.

Authors:  Sabrina Petralla; Cristina Parenti; Valentina Ravaioli; Irene Fancello; Francesca Massenzio; Marco Virgili; Barbara Monti; Emiliano Pena-Altamira
Journal:  Mol Neurobiol       Date:  2020-11-09       Impact factor: 5.590

7.  Mitochondrial dysfunction in platelets and hippocampi of senescence-accelerated mice.

Authors:  Jie Xu; Chun Shi; Qi Li; Jiajia Wu; E Lucy Forster; David T Yew
Journal:  J Bioenerg Biomembr       Date:  2007-04-14       Impact factor: 3.853

8.  Mechanisms of aging in senescence-accelerated mice.

Authors:  Todd A Carter; Jennifer A Greenhall; Shigeo Yoshida; Sebastian Fuchs; Robert Helton; Anand Swaroop; David J Lockhart; Carrolee Barlow
Journal:  Genome Biol       Date:  2005-06-01       Impact factor: 13.583

9.  Exome sequencing of senescence-accelerated mice (SAM) reveals deleterious mutations in degenerative disease-causing genes.

Authors:  Kumpei Tanisawa; Eri Mikami; Noriyuki Fuku; Yoko Honda; Shuji Honda; Ikuro Ohsawa; Masafumi Ito; Shogo Endo; Kunio Ihara; Kinji Ohno; Yuki Kishimoto; Akihito Ishigami; Naoki Maruyama; Motoji Sawabe; Hiroyoshi Iseki; Yasushi Okazaki; Sanae Hasegawa-Ishii; Shiro Takei; Atsuyoshi Shimada; Masanori Hosokawa; Masayuki Mori; Keiichi Higuchi; Toshio Takeda; Mitsuru Higuchi; Masashi Tanaka
Journal:  BMC Genomics       Date:  2013-04-15       Impact factor: 3.969

10.  Alterations in local thyroid hormone signaling in the hippocampus of the SAMP8 mouse at younger ages: association with delayed myelination and behavioral abnormalities.

Authors:  Erika Sawano; Takayuki Negishi; Tomoyuki Aoki; Masami Murakami; Tomoko Tashiro
Journal:  J Neurosci Res       Date:  2012-12-06       Impact factor: 4.164

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.