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  Contractile characteristics of gastrocnemius-soleus muscle in the SOD1G93A ALS mouse model.

Dibaj, P., Schomburg, E. D., & Steffens, H. (2015). Contractile characteristics of gastrocnemius-soleus muscle in the SOD1G93A ALS mouse model. Neurological Research, 37(8), 693-702. doi:10.1179/1743132815Y.0000000039.

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資料種別: 学術論文

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 作成者:
Dibaj, P., 著者
Schomburg, E. D., 著者
Steffens, H.1, 著者           
所属:
1Department of NanoBiophotonics, MPI for biophysical chemistry, Max Planck Society, ou_578627              

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キーワード: Amyotrophic lateral sclerosis; SOD1G93A ALS mouse model; Muscle contractile force; Fibre relaxation; Twitch fusion; Potentiation and fatigue
 要旨: Objectives: In the SOD1G93A mouse model of amyotrophic lateral sclerosis (ALS), a selective degeneration of fast-fatigable motor units and consequently an early decline of contractile force in individual fast-twitch muscles have been observed in the preclinical stage. However, most human muscles include fast and slow motor units. Gastrocnemius-soleus group (GS) contains such a mixture of units. Methods: We have investigated changes in the mechanical properties of GS at different SOD1G93A stages in mice. For this purpose, the tibial nerve was repetitively stimulated with rectangular pulses and the force of GS twitches was recorded using a strain gauge fixed to the Achilles tendon. Results: Isometric and tetanic force were attenuated but not before the first clinical signs developed. However, already at preclinical stages, single twitches showed a slower decay compared to control. Consequently, fusion of GS twitches occurred at lower stimulus rates. Furthermore, already preclinically, the temporal course of successive twitch amplitudes changed during repetitive stimulation at increasing rates. The peak amplitudes as well as the potentiation following decay (fatigue) were lower in preclinical mice than in control. Discussion: The time-lapse analysis of the contractile pattern as well as of the twitch configuration of the mixed muscle GS have revealed distinctive differences between wild-type controls and preclinical SOD1G93A mice. It would be of interest to know whether these preclinical changes are also detectable in ALS patients.

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言語: eng - English
 日付: 2015-08
 出版の状態: 出版
 ページ: -
 出版情報: -
 目次: -
 査読: 査読あり
 識別子(DOI, ISBNなど): DOI: 10.1179/1743132815Y.0000000039
 学位: -

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出版物 1

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出版物名: Neurological Research
種別: 学術雑誌
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所属:
出版社, 出版地: -
ページ: - 巻号: 37 (8) 通巻号: - 開始・終了ページ: 693 - 702 識別子(ISBN, ISSN, DOIなど): -