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Muscle atrophy and regeneration associated with behavioural loss and recovery of function after sciatic nerve crush

Grönholdt-Klein, Max (författare)
Karolinska Inst, Dept Neurosci, S-17177 Stockholm, Sweden
Altun, Mikael (författare)
Karolinska Institutet
Becklen, Meneca (författare)
Karolinska Inst, Dept Neurosci, S-17177 Stockholm, Sweden
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Kahm, Emelie Dickman (författare)
Karolinska Inst, Dept Neurosci, S-17177 Stockholm, Sweden
Fahlström, Andreas (författare)
Uppsala universitet,Enblad: Neurokirurgi,Karolinska Inst, Dept Neurosci, S-17177 Stockholm, Sweden
Rullman, Eric (författare)
Karolinska Institutet
Ulfhake, Brun (författare)
Karolinska Institutet
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 (creator_code:org_t)
2019-07-02
2019
Engelska.
Ingår i: Acta Physiologica. - : John Wiley & Sons. - 1748-1708 .- 1748-1716. ; 227:3
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Aim To resolve timing and coordination of denervation atrophy and the re-innervation recovery process to discern correlations indicative of common programs governing these processes. Methods Female Sprague-Dawley (SD) rats had a unilateral sciatic nerve crush. Based on longitudinal behavioural observations, the triceps surae muscle was analysed at different time points post-lesion. Results Crush results in a loss of muscle function and mass (-30%) followed by a recovery to almost pre-lesion status at 30 days post-crush (dpc). There was no loss of fibres nor any significant change in the number of nuclei per fibre but a shift in fibres expressing myosins I and II that reverted back to control levels at 30 dpc. A residual was the persistence of hybrid fibres. Early on a CHNR -epsilon to -gamma switch and a re-expression of embryonic MyHC showed as signs of denervation. Foxo1, Smad3, Fbxo32 and Trim63 transcripts were upregulated but not Myostatin, InhibinA and ActivinR2B. Combined this suggests that the mechanism instigating atrophy provides a selectivity of pathway(s) activated. The myogenic differentiation factors (MDFs: Myog, Myod1 and Myf6) were upregulated early on suggesting a role also in the initial atrophy. The regulation of these transcripts returned towards baseline at 30 dpc. The examined genes showed a strong baseline covariance in transcript levels which dissolved in the response to crush driven mainly by the MDFs. At 30 dpc the naive expression pattern was re-established. Conclusion Peripheral nerve crush offers an excellent model to assess and interfere with muscle adaptions to denervation and re-innervation.

Ämnesord

NATURVETENSKAP  -- Biologi -- Cellbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Cell Biology (hsv//eng)

Nyckelord

denervation
muscle atrophy
muscle regeneration
re-innervation
rodent

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