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Localization of calcium‐accumulating structures in the anterior byssal retractor muscle of Mytilus edulis and their role in the regulation of active and catch contractions.
Author(s) -
Atsumi S,
Sugi H
Publication year - 1976
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.1976.sp011384
Subject(s) - mytilus , biophysics , calcium , contraction (grammar) , chemistry , endoplasmic reticulum , byssus , acetylcholine , vesicle , membrane , medicine , endocrinology , biochemistry , biology , ecology , organic chemistry
1. The localization of Ca‐accumulating structures in the anterior byssal retractor muscle (ABRM) of Mytilus edulis and their role in the contraction‐relaxation cycle were studied by fixing the ABRM at rest or during various phases of mechanical activity with a 1% osmium tetroxide solution containing 2% potassium pyroantimonate. 2. In the resting ABRM, electron‐opaque pyroantimonate precipitate was observed at the inner surface of the plasma membrane, the vesicles and the mitochondria. 3. Electron X‐ray microanalysis showed the presence of Ca in the precipitate, indicating that the precipitate provides a valid measure for Ca localization. 4. In the ABRM fixed at the peak of mechanical response to the Ca‐removal or to acetylcholine, the precipitate was found to be diffusely distributed in the myoplasm in the form of a number of particles. At the completion of spontaneous relaxation, the precipitate was again seen at the inner surface of the plasma membrane. 5. During the catch state, the precipitate was found to be re‐accumulated in the peripheral structures with a corresponding decrease of the precipitate in the myoplasm. 6. These results not only provide evidence for the involvement of the Ca‐accumulating structures in the contraction‐relaxation cycle in the ABRM, but also suggest that the transition from active to catch contractions is related to a decrease in myoplasmic free Ca ion concentration.

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