Shortening deactivation: quantifying a critical component of cyclical muscle contraction

Author:

Loya Amy K.1,Van Houten Sarah K.2,Glasheen Bernadette M.3,Swank Douglas M.4

Affiliation:

1. Department of Biomedical Engineering 8 Center for Biotechnology and Interdisciplinary Studies Rensselaer Polytechnic Institute 110 8th Street, Troy, NY 12180; Department of Electrical, Computer, and Biomedical Engineering Union College 807 Union Street, Schenectady, NY 12308, Schenectady, NY, United States

2. Department of Biomedical Engineering 8 Center for Biotechnology and Interdisciplinary Studies Rensselaer Polytechnic Institute 110 8th Street, Troy, NY 12180, Troy, NY, United States

3. Department of Biological Sciences Center for Biotechnology and Interdisciplinary Studies Rensselaer Polytechnic Institute 110 8th Street, Troy, NY 12180, United States

4. Department of Biomedical Engineering 8 Center for Biotechnology and Interdisciplinary Studies Rensselaer Polytechnic Institute 110 8th Street, Troy, NY 12180; Department of Biological Sciences Center for Biotechnology and Interdisciplinary Studies Rensselaer Polytechnic Institute 110 8th Street, Troy, NY 12180, Troy, NY, United States

Abstract

A muscle undergoing cyclical contractions requires fast and efficient muscle activation and relaxation to generate high power with relatively low energetic cost. To enhance activation and increase force levels during shortening, some muscle types have evolved stretch activation (SA), a delayed increased in force following rapid muscle lengthening. SA's complementary phenomenon is shortening deactivation (SD), a delayed decrease in force following muscle shortening. SD increases muscle relaxation, which decreases resistance to subsequent muscle lengthening. While it might be just as important to cyclical power output, SD has received less investigation than SA. To enable mechanistic investigations into SD and quantitatively compare it to SA, we developed a protocol to elicit SA and SD from Drosophila and Lethocerus indirect flight muscles (IFM) and Drosophila jump muscle. When normalized to isometric tension, Drosophila IFM exhibited a 118% SD tension decrease, Lethocerus IFM dropped by 97%, and Drosophila jump muscle decreased by 37%. The same order was found for normalized SA tension: Drosophila IFM increased by 233%, Lethocerus IFM by 76%, and Drosophila jump muscle by only 11%. SD occurred slightly earlier than SA, relative to the respective length change, for both IFMs; but SD was exceedingly earlier than SA for jump muscle. Our results suggest SA and SD evolved to enable highly efficient IFM cyclical power generation and may be caused by the same mechanism. However, jump muscle SA and SD mechanisms are likely different, and may have evolved for a role other than to increase the power output of cyclical contractions.

Funder

HHS | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases

Publisher

American Physiological Society

Subject

Cell Biology,Physiology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The self-oscillation paradox in the flight motor ofDrosophila melanogaster;Journal of The Royal Society Interface;2023-11

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