Denervation alters myosin heavy chain expression and contractility of developing rat diaphragm muscle
Journal of Applied Physiology, ISSN: 8750-7587, Vol: 89, Issue: 3, Page: 1106-1113
2000
- 30Citations
- 17Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations30
- Citation Indexes30
- 30
- CrossRef29
- Captures17
- Readers17
- 17
Article Description
We hypothesized that unilateral denervation (DNV) of the rat diaphragm muscle (Dia) in neonates at postnatal day 7 (D-7) alters normal transitions of myosin heavy chain (MHC) isoform expression and thereby affects postnatal changes in maximum specific force (P) and maximum unloaded shortening velocity (V). The relative expression of different MHC isoforms was analyzed electrophoretically. With DNV at D-7, expression of MHC in the Dia persisted, and emergence of MHC and MHC was delayed. By D-21 and D-28, relative expression of MHC and MHC was reduced in DNV compared with control (CTL) animals. Expression of MHC also reappeared in adult Dia by 2-3 wk after DNV, and relative expression of MHC was reduced. At each age, P was reduced and V was slowed by DNV, compared with CTL. In CTL Dia, postnatal changes in P and V were associated with an increase in fast MHC isoform expression. In DNV Dia, no such association existed. We conclude that, in the Dia, DNV induces alterations in both MHC isoform expression and contractile properties, which are not necessarily causally linked.
Bibliographic Details
American Physiological Society
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