Literature DB >> 18264714

Subcutaneous injection, from birth, of epigallocatechin-3-gallate, a component of green tea, limits the onset of muscular dystrophy in mdx mice: a quantitative histological, immunohistochemical and electrophysiological study.

Yoshiko Nakae1, Katsuya Hirasaka, Junpei Goto, Takeshi Nikawa, Masayuki Shono, Mizuko Yoshida, Peter J Stoward.   

Abstract

Dystrophic muscles suffer from enhanced oxidative stress. We have investigated whether administration of an antioxidant, epigallocatechin-3-gallate (EGCG), a component of green tea, reduces their oxidative stress and pathophysiology in mdx mice, a mild phenotype model of human Duchenne-type muscular dystrophy. EGCG (5 mg/kg body weight in saline) was injected subcutaneously 4x a week into the backs of C57 normal and dystrophin-deficient mdx mice for 8 weeks after birth. Saline was injected into normal and mdx controls. EGCG had almost no observable effects on normal mice or on the body weights of mdx mice. In contrast, it produced the following improvements in the blood chemistry, muscle histology, and electrophysiology of the treated mdx mice. First, the activities of serum creatine kinase were reduced to normal levels. Second, the numbers of fluorescent lipofuscin granules per unit volume of soleus and diaphragm muscles were significantly decreased by about 50% compared to the numbers in the corresponding saline-treated controls. Third, in sections of diaphragm and soleus muscles, the relative area occupied by histologically normal muscle fibres increased significantly 1.5- to 2-fold whereas the relative areas of connective tissue and necrotic muscle fibres were substantially reduced. Fourth, the times for the maximum tetanic force of soleus muscles to fall by a half increased to almost normal values. Fifth, the amount of utrophin in diaphragm muscles increased significantly by 17%, partially compensating for the lack of dystrophin expression.

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Year:  2008        PMID: 18264714     DOI: 10.1007/s00418-008-0390-2

Source DB:  PubMed          Journal:  Histochem Cell Biol        ISSN: 0948-6143            Impact factor:   4.304


  47 in total

1.  Muscle and neural isoforms of agrin increase utrophin expression in cultured myotubes via a transcriptional regulatory mechanism.

Authors:  A O Gramolini; E A Burton; J M Tinsley; M J Ferns; A Cartaud; J Cartaud; K E Davies; J A Lunde; B J Jasmin
Journal:  J Biol Chem       Date:  1998-01-09       Impact factor: 5.157

2.  Full functional rescue of a complete muscle (TA) in dystrophic hamsters by adeno-associated virus vector-directed gene therapy.

Authors:  X Xiao; J Li; Y P Tsao; D Dressman; E P Hoffman; J F Watchko
Journal:  J Virol       Date:  2000-02       Impact factor: 5.103

Review 3.  Function and genetics of dystrophin and dystrophin-related proteins in muscle.

Authors:  Derek J Blake; Andrew Weir; Sarah E Newey; Kay E Davies
Journal:  Physiol Rev       Date:  2002-04       Impact factor: 37.312

Review 4.  Dystrophin, its interactions with other proteins, and implications for muscular dystrophy.

Authors:  James M Ervasti
Journal:  Biochim Biophys Acta       Date:  2006-06-07

5.  Sarcolemmal damage in dystrophin deficiency is modulated by synergistic interactions between mechanical and oxidative/nitrosative stresses.

Authors:  Roy W R Dudley; Gawiyou Danialou; Karuthapillai Govindaraju; Larry Lands; David E Eidelman; Basil J Petrof
Journal:  Am J Pathol       Date:  2006-04       Impact factor: 4.307

Review 6.  The role of free radicals in the pathophysiology of muscular dystrophy.

Authors:  James G Tidball; Michelle Wehling-Henricks
Journal:  J Appl Physiol (1985)       Date:  2006-11-09

7.  The role of reactive oxygen species in the hearts of dystrophin-deficient mdx mice.

Authors:  Iwan A Williams; David G Allen
Journal:  Am J Physiol Heart Circ Physiol       Date:  2007-06-15       Impact factor: 4.733

8.  Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscle.

Authors:  A Clerk; G E Morris; V Dubowitz; K E Davies; C A Sewry
Journal:  Histochem J       Date:  1993-08

9.  Evidence of oxidative stress in mdx mouse muscle: studies of the pre-necrotic state.

Authors:  M H Disatnik; J Dhawan; Y Yu; M F Beal; M M Whirl; A A Franco; T A Rando
Journal:  J Neurol Sci       Date:  1998-11-26       Impact factor: 3.181

10.  The effect of glucocorticoids on the accumulation of utrophin by cultured normal and dystrophic human skeletal muscle satellite cells.

Authors:  F Pasquini; C Guerin; D Blake; K Davies; G Karpati; P Holland
Journal:  Neuromuscul Disord       Date:  1995-03       Impact factor: 4.296

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  26 in total

Review 1.  What has the mdx mouse model of Duchenne muscular dystrophy contributed to our understanding of this disease?

Authors:  Jennifer Manning; Dervla O'Malley
Journal:  J Muscle Res Cell Motil       Date:  2015-02-11       Impact factor: 2.698

Review 2.  State-of-the-art technologies, current opinions and developments, and novel findings: news from the field of histochemistry and cell biology.

Authors:  Esther Asan; Detlev Drenckhahn
Journal:  Histochem Cell Biol       Date:  2008-11-05       Impact factor: 4.304

3.  Green tea catechins are potent sensitizers of ryanodine receptor type 1 (RyR1).

Authors:  Wei Feng; Gennady Cherednichenko; Chris W Ward; Isela T Padilla; Elaine Cabrales; José R Lopez; José M Eltit; Paul D Allen; Isaac N Pessah
Journal:  Biochem Pharmacol       Date:  2010-05-22       Impact factor: 5.858

4.  Quantification of ceroid and lipofuscin in skeletal muscle.

Authors:  Hatice Tohma; Anna R Hepworth; Thea Shavlakadze; Miranda D Grounds; Peter G Arthur
Journal:  J Histochem Cytochem       Date:  2011-08       Impact factor: 2.479

5.  Identification of retinoic acid in a high content screen for agents that overcome the anti-myogenic effect of TGF-beta-1.

Authors:  Chateen Krueger; F Michael Hoffmann
Journal:  PLoS One       Date:  2010-11-30       Impact factor: 3.240

6.  Endurance capacity in maturing mdx mice is markedly enhanced by combined voluntary wheel running and green tea extract.

Authors:  Jarrod A Call; Kevin A Voelker; Andrew V Wolff; Ryan P McMillan; Nick P Evans; Matthew W Hulver; Robert J Talmadge; Robert W Grange
Journal:  J Appl Physiol (1985)       Date:  2008-06-26

Review 7.  Immune-mediated mechanisms potentially regulate the disease time-course of duchenne muscular dystrophy and provide targets for therapeutic intervention.

Authors:  Nicholas P Evans; Sarah A Misyak; John L Robertson; Josep Bassaganya-Riera; Robert W Grange
Journal:  PM R       Date:  2009-08       Impact factor: 2.298

8.  The Dietary Supplement Protandim Decreases Plasma Osteopontin and Improves Markers of Oxidative Stress in Muscular Dystrophy Mdx Mice.

Authors:  Muhammad Muddasir Qureshi; Warren C McClure; Nicole L Arevalo; Rick E Rabon; Benjamin Mohr; Swapan K Bose; Joe M McCord; Brian S Tseng
Journal:  J Diet Suppl       Date:  2010-06-01

9.  Green tea extract decreases muscle pathology and NF-kappaB immunostaining in regenerating muscle fibers of mdx mice.

Authors:  Nicholas P Evans; Jarrod A Call; Josep Bassaganya-Riera; John L Robertson; Robert W Grange
Journal:  Clin Nutr       Date:  2009-11-07       Impact factor: 7.324

Review 10.  Contribution of oxidative stress to pathology in diaphragm and limb muscles with Duchenne muscular dystrophy.

Authors:  Jong-Hee Kim; Hyo-Bum Kwak; LaDora V Thompson; John M Lawler
Journal:  J Muscle Res Cell Motil       Date:  2012-10-28       Impact factor: 2.698

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