Literature DB >> 6714329

Cataract and other ophthalmic lesions in senescence accelerated mouse (SAM). Morphology and incidence of senescence associated ophthalmic changes in mice.

M Hosokawa, S Takeshita, K Higuchi, K Shimizu, M Irino, K Toda, A Honma, A Matsumura, K Yasuhira, T Takeda.   

Abstract

In a murine model of accelerated senescence (SAM), grading score and incidence in cataract, periophthalmic lesions, opacity and ulcer of the cornea were determined in mice from 4 to 24 months of age. From 4 to 6 months of age, incidence and grading score of these four categories began to increase in both the accelerated senescence prone (SAM) and resistant series with normal aging, and these increases continued with aging. As compared with the resistant series, there was a higher incidence and grading score of the four categories and a higher rate of increase in the prone series. The prone 3 series in particular showed a much higher incidence and grading score on cataract, the rate being 27.5% and 70.6% at 12 and 16 months, respectively. Histologically, the cataract was classified into two types. In one, degeneration of lens fibers, disintegration of lens cortex, and at an advanced stage, liquefaction of the lens cortex and proliferation of the anterior lens epithelial cells occurred. In the other type, lens fibers lost their distinct shapes and a homogenous mass formed at the anterior and posterior superficial cortex. The anterior lens epithelial cells had shrunk. There was an opacity and ulcer of the cornea with keratitis and the corneal epithelium was lost in case of the latter. Periophthalmic lesions included catarrhal changes of the skin of the eyelids and face and blepharitis. There were no lesions specific to each of the prone and resistant series. Thus, SAM should prove to be a suitable murine model for investigation of age-related ophthalmic lesions, including cataract in humans.

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Year:  1984        PMID: 6714329     DOI: 10.1016/0014-4835(84)90095-2

Source DB:  PubMed          Journal:  Exp Eye Res        ISSN: 0014-4835            Impact factor:   3.467


  14 in total

1.  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

2.  High incidence of spontaneous cataracts in aging laboratory rabbits of an inbred strain.

Authors:  Xuwen Peng; Sara Roshwalb; Timothy K Cooper; Heather Zimmerman; Neil D Christensen
Journal:  Vet Ophthalmol       Date:  2014-08-14       Impact factor: 1.644

3.  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

4.  Morphological study of the cataractous lens of the senescence accelerated mouse.

Authors:  H Nishimoto; S Uga; M Miyata; S Ishikawa; K Yamashita
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1993-12       Impact factor: 3.117

5.  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

6.  Morphologic demonstration of cytoplasmic ASSAM-related antigenic substance (CASSAM) by an immunoperoxidase technique.

Authors:  S Takeshita; K Higuchi; M Hosokawa; A Matsumura; K Higuchi; A Kohno; M Matsushita; T Yonezu; T Takeda
Journal:  Am J Pathol       Date:  1985-12       Impact factor: 4.307

7.  Immunocytochemical evaluation of the blood-brain barrier to endogenous albumin in the olfactory bulb and pons of senescence-accelerated mice (SAM).

Authors:  M Ueno; D H Dobrogowska; A W Vorbrodt
Journal:  Histochem Cell Biol       Date:  1996-03       Impact factor: 4.304

8.  Immune responses in newly developed short-lived SAM mice. I. Age-associated early decline in immune activities of cultured spleen cells.

Authors:  T Hosokawa; M Hosono; K Higuchi; A Aoike; K Kawai; T Takeda
Journal:  Immunology       Date:  1987-11       Impact factor: 7.397

9.  Periodic acid-Schiff (PAS)-positive, granular structures increase in the brain of senescence accelerated mouse (SAM).

Authors:  H Akiyama; M Kameyama; I Akiguchi; H Sugiyama; T Kawamata; H Fukuyama; H Kimura; M Matsushita; T Takeda
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

10.  Monoamine oxidase-B-positive granular structures in the hippocampus of aged senescence-accelerated mouse (SAMP8).

Authors:  S Nakamura; I Akiguchi; N Seriu; K Ohnishi; M Takemura; M Ueno; H Tomimoto; T Kawamata; J Kimura; M Hosokawa
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

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