Literature DB >> 6748759

Grading score system: a method for evaluation of the degree of senescence in senescence accelerated mouse (SAM).

M Hosokawa, R Kasai, K Higuchi, S Takeshita, K Shimizu, H Hamamoto, A Honma, M Irino, K Toda, A Matsumura.   

Abstract

For evaluation of the degree of senescence in SAM-P, accelerated senescence prone mouse, formerly called SAM or prone series or P-series, consisting of SAM-P/1, SAM-P/2, SAM-P/3 and SAM-P/4 corresponding to P-1, P-2, P-3 and P-4 series, respectively, in the previous reports, and in SAM-R, accelerated senescence resistant mouse, formerly called resistant series or R-series, consisting of SAM-R/1, SAM-R/2 and SAM-R/3 corresponding to R-1, R-2 and R-3 series, respectively, in the previous reports, the grading score system was adopted. The items to be examined in this system include 11 categories selected from the clinical signs and gross lesions considered to be associated with the aging process. The degree of the senescence in each category was graded from 0 to 4 according to the detailed criteria devised in our laboratory. After 8 months of age each mouse was examined every 4 months, and some of the mice were examined after 2 months of age. In almost all categories, the grading score and incidence began to increase from 4 or 6 months of age and continued to increase with advancing age in both SAM-P and SAM-R. The increase, however, was more marked in SAM-P than in SAM-R. The slow but steady increase in the SAM-R levelled out at 24 months of age and was comparable to that at 12 months of age in SAM-P. In both SAM-P/1 at 8 months of age and SAM-R/2 at 12 months of age, there was a significant reverse correlation between total score of this grading score system and length of residual life after examination. Systematic and extensive studies using the grading score system showed that if the validity of the system is, based on "irreversibility" and "universality" of the changes in each category with advancing age, most categories are valid for evaluation of the degree of senescence. This grading score system is a unique, useful and convenient method for evaluation of the degree of senescence in mice.

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Year:  1984        PMID: 6748759     DOI: 10.1016/0047-6374(84)90168-4

Source DB:  PubMed          Journal:  Mech Ageing Dev        ISSN: 0047-6374            Impact factor:   5.432


  39 in total

1.  Comparative studies of early liver dysfunction in senescence-accelerated mouse using mitochondrial proteomics approaches.

Authors:  Yashu Liu; Jintang He; Shaoyi Ji; Qingsong Wang; Hai Pu; Tingting Jiang; Lingyao Meng; Xiuwei Yang; Jianguo Ji
Journal:  Mol Cell Proteomics       Date:  2008-05-29       Impact factor: 5.911

2.  Hippocampal neuron loss is correlated with cognitive deficits in SAMP8 mice.

Authors:  Guomin Li; Haiyan Cheng; Xuezhu Zhang; Xuemei Shang; Hui Xie; Xin Zhang; Jianchun Yu; Jingxian Han
Journal:  Neurol Sci       Date:  2012-08-08       Impact factor: 3.307

3.  Immune responses in newly developed short-lived SAM mice. III. Genetic control of defective helper T-cell activity in in vitro primary antibody response.

Authors:  K Hanada; M Hosono; T Hosokawa; W E Chen; T Tsuboyama; T Takeda
Journal:  Immunology       Date:  1989-12       Impact factor: 7.397

4.  Astrocytes and neurons produce distinct types of polyglucosan bodies in Lafora disease.

Authors:  Elisabet Augé; Carme Pelegrí; Gemma Manich; Itsaso Cabezón; Joan J Guinovart; Jordi Duran; Jordi Vilaplana
Journal:  Glia       Date:  2018-08-26       Impact factor: 7.452

5.  Practical methodology of evaluation of mortality curves and detection of aging-related interventions.

Authors:  S Doubal; P Klemera
Journal:  Age (Omaha)       Date:  1997-10

6.  Molecular cloning and nucleotide sequence of cDNA for murine senile amyloid protein: nucleotide substitutions found in apolipoprotein A-II cDNA of senescence accelerated mouse (SAM).

Authors:  T Kunisada; K Higuchi; S Aota; T Takeda; H Yamagishi
Journal:  Nucleic Acids Res       Date:  1986-07-25       Impact factor: 16.971

7.  TMJ degeneration in SAMP8 mice is accompanied by deranged Ihh signaling.

Authors:  Y Ishizuka; Y Shibukawa; M Nagayama; R Decker; T Kinumatsu; A Saito; M Pacifici; E Koyama
Journal:  J Dent Res       Date:  2014-01-22       Impact factor: 6.116

8.  Age-related changes in the temporomandibular joint of the senescence accelerated mouse. SAM-P/3 as a new murine model of degenerative joint disease.

Authors:  W H Chen; M Hosokawa; T Tsuboyama; T Ono; T Iizuka; T Takeda
Journal:  Am J Pathol       Date:  1989-08       Impact factor: 4.307

9.  Age-related changes in bone mass in the senescence-accelerated mouse (SAM). SAM-R/3 and SAM-P/6 as new murine models for senile osteoporosis.

Authors:  M Matsushita; T Tsuboyama; R Kasai; H Okumura; T Yamamuro; K Higuchi; K Higuchi; A Kohno; T Yonezu; A Utani
Journal:  Am J Pathol       Date:  1986-11       Impact factor: 4.307

10.  An acceleration of age-related increases in levels of the beta-subunit of nerve growth factor in selected tissues from senescence-accelerated mice (SAM-P/8).

Authors:  R Katoh-Semba; R Semba; S Kashiwamata; K Kato
Journal:  J Mol Neurosci       Date:  1993       Impact factor: 3.444

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