Bojungikgi-tang Improves Muscle and Spinal Cord Function in an Amyotrophic Lateral Sclerosis Model

被引:24
作者
Cai, MuDan [1 ]
Lee, Sun Hwa [1 ]
Yang, Eun Jin [1 ]
机构
[1] Korea Inst Oriental Med, Dept Clin Res, 1672 Yuseong Daero, Daejeon 305811, South Korea
基金
新加坡国家研究基金会;
关键词
Amyotrophic lateral sclerosis; Bojungikgi-tang; Motor function; Muscle atrophy; HOCHU-EKKI-TO; YI-QI-TANG; SKELETAL-MUSCLE; MOUSE MODEL; DISEASE PROGRESSION; MOTOR-NEURONS; HERBAL MEDICINE; ALS MICE; MECHANISMS; DEGENERATION;
D O I
10.1007/s12035-018-1236-0
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Amyotrophic lateral sclerosis (ALS) is a motor neuron disease characterized by progressive motor function impairment, dysphagia, and respiratory failure. Owing to the complexity of its pathogenic mechanisms, an effective therapy for ALS is lacking. Herbal medicines with multiple targets have good efficacy and low adverse reactions for the treatment of neurodegenerative diseases. In this study, the effects of Bojungikgi-tang (BJIGT), an herbal medicine with eight component herbs, on muscle and spinal cord function were evaluated in an ALS animal model. Animals were randomly divided into three groups: a non-transgenic group (nTg, n=24), a hSOD1(G93A) transgenic group (Tg, n=24), and a hSOD1(G93A) transgenic group in which 8-week-old mice were orally administered BJIGT (1mg/g) once daily for 6weeks (Tg+BJIGT, n=24). The effects of BJIGT were evaluated using a rotarod test, foot-printing, and survival analyses based on Kaplan-Meier survival curves. To determine the biological mechanism underlying the effects of BJIGT in hSOD1(G93A) mice, western blotting, transmission electron microscopy, and Bungarotoxin staining were used. BJIGT improved motor function and extended the survival duration of hSOD1(G93A) mice. In addition, BJIGT had protective effects, including anti-oxidative and anti-inflammatory effects, in both the spinal cord and muscle of hSOD1(G93A) mice. Our results demonstrated that BJIGT causes muscle atrophy and the denervation of neuromuscular junctions in the gastrocnemius of hSOD1(G93A) mice. The components of BJIGT may alleviate the symptoms of ALS via different mechanisms, and accordingly, BJIGT treatment may be an effective therapeutic approach.
引用
收藏
页码:2394 / 2407
页数:14
相关论文
共 68 条
[1]
Cellular and molecular mechanisms of muscle atrophy [J].
Bonaldo, Paolo ;
Sandri, Marco .
DISEASE MODELS & MECHANISMS, 2013, 6 (01) :25-39
[2]
Borthwick GM, 1999, ANN NEUROL, V46, P787, DOI 10.1002/1531-8249(199911)46:5<787::AID-ANA17>3.0.CO
[3]
2-8
[4]
Wnt signaling during synaptic development and plasticity [J].
Budnik, Vivian ;
Salinas, Patricia C. .
CURRENT OPINION IN NEUROBIOLOGY, 2011, 21 (01) :151-159
[5]
The Effects of Bee Venom Acupuncture on the Central Nervous System and Muscle in an Animal hSOD1G93A Mutant [J].
Cai, MuDan ;
Choi, Sun-Mi ;
Yang, Eun Jin .
TOXINS, 2015, 7 (03) :846-858
[6]
Wnt Signaling in Skeletal Muscle Dynamics: Myogenesis, Neuromuscular Synapse and Fibrosis [J].
Cisternas, Pedro ;
Henriquez, Juan P. ;
Brandan, Enrique ;
Inestrosa, Nibaldo C. .
MOLECULAR NEUROBIOLOGY, 2014, 49 (01) :574-589
[7]
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction [J].
Corti, Stefania ;
Donadoni, Chiara ;
Ronchi, Dario ;
Bordoni, Andreina ;
Fortunato, Francesco ;
Santoro, Domenico ;
Del Bo, Roberto ;
Lucchini, Valeria ;
Crugnola, Veronica ;
Papadimitriou, Dimitra ;
Salani, Sabrina ;
Moggio, Maurizio ;
Bresolin, Nereo ;
Comi, Giacomo P. .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2009, 276 (1-2) :170-174
[8]
Differential autophagy power in the spinal cord and muscle of transgenic ALS mice [J].
Crippa, Valeria ;
Boncoraglio, Alessandra ;
Galbiati, Mariarita ;
Aggarwal, Tanya ;
Rusmini, Paola ;
Giorgetti, Elisa ;
Cristofani, Riccardo ;
Carra, Serena ;
Pennuto, Maria ;
Poletti, Angelo .
FRONTIERS IN CELLULAR NEUROSCIENCE, 2013, 7
[9]
Neuroinflammation in Amyotrophic Lateral Sclerosis: Role of Redox (dys)Regulation [J].
D'Ambrosi, Nadia ;
Cozzolino, Mauro ;
Carri, Maria Teresa .
ANTIOXIDANTS & REDOX SIGNALING, 2018, 29 (01) :15-36
[10]
Skeletal Muscle Is a Primary Target of SOD1G93A-Mediated Toxicity [J].
Dobrowolny, Gabriella ;
Aucello, Michela ;
Rizzuto, Emanuele ;
Beccafico, Sara ;
Mammucari, Cristina ;
Bonconpagni, Simona ;
Belia, Silvia ;
Wannenes, Francesca ;
Nicoletti, Carmine ;
Del Prete, Zaccaria ;
Rosenthal, Nadia ;
Molinaro, Mario ;
Protasi, Feliciano ;
Fano, Giorgio ;
Sandri, Marco ;
Musaro, Antonio .
CELL METABOLISM, 2008, 8 (05) :425-436