Abstract
Membrane constants and distribution of acetylcholine (ACh) receptors were determined for multiply innervated fibers of the anterior latissimus dorsi (ALD) and singly innervated fibers of the posterior latissimus dorsi (PLD) muscles of 3–6 month old chickens. The values of the various membrane constants were: length constant, 1.78 mm (mean) in ALD, 0.68 mm in PLD; time constant, 35 msec in ALD, 3.7 msec in PLD; transverse membrane resistance, 4388 Ω cm2 in ALD, 561 Ω cm2 in PLD; and membrane capacitance, 8.2 µF/cm2 in ALD, 7.0 µF/cm2 in PLD. Peaks of ACh sensitivity occurred at intervals of ca. 740 µ on ALD fibers with a low sensitivity remaining between peaks. Only one peak of ACh sensitivity was detected on PLD fibers. The maximum ACh sensitivity found was 5 ± 4 mv/ncoul for fibers of the ALD and 77 ± 60 mv/ncoul for fibers of the PLD. The distance over which this sensitivity fell to 0.1 was ca. 225 µ in the ALD and 140 µ in the PLD. The membranes of these two muscle fiber types differ widely regarding some electrical properties and the disposition of ACh-sensitive receptor sites.
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- BOYD I. A., MARTIN A. R. Membrane constants of mammalian muscle fibres. J Physiol. 1959 Oct;147:450–457. doi: 10.1113/jphysiol.1959.sp006255. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BULLER A. J., ECCLES J. C., ECCLES R. M. Interactions between motoneurones and muscles in respect of the characteristic speeds of their responses. J Physiol. 1960 Feb;150:417–439. doi: 10.1113/jphysiol.1960.sp006395. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DEL CASTILLO J., KATZ B. On the localization of acetylcholine receptors. J Physiol. 1955 Apr 28;128(1):157–181. doi: 10.1113/jphysiol.1955.sp005297. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DEL CASTILLO J., MACHNE X. Effect of temperature on the passive electrical properties of the muscle fibre membrane. J Physiol. 1953 May 28;120(3):431–434. doi: 10.1113/jphysiol.1953.sp004906. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eisenberg R. S., Gage P. W. Frog skeletal muscle fibers: changes in electrical properties after disruption of transverse tubular system. Science. 1967 Dec 29;158(3809):1700–1701. doi: 10.1126/science.158.3809.1700. [DOI] [PubMed] [Google Scholar]
- FALK G., FATT P. LINEAR ELECTRICAL PROPERTIES OF STRIATED MUSCLE FIBRES OBSERVED WITH INTRACELLULAR ELECTRODES. Proc R Soc Lond B Biol Sci. 1964 Apr 14;160:69–123. doi: 10.1098/rspb.1964.0030. [DOI] [PubMed] [Google Scholar]
- FATT P. AN ANALYSIS OF THE TRANSVERSE ELECTRICAL IMPEDANCE OF STRIATED MUSCLE. Proc R Soc Lond B Biol Sci. 1964 Mar 17;159:606–651. doi: 10.1098/rspb.1964.0023. [DOI] [PubMed] [Google Scholar]
- FATT P., KATZ B. An analysis of the end-plate potential recorded with an intracellular electrode. J Physiol. 1951 Nov 28;115(3):320–370. doi: 10.1113/jphysiol.1951.sp004675. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Freygang W. H., Jr, Rapoport S. I., Peachey L. D. Some relations between changes in the linear electrical properties of striated muscle fibers and changes in ultrastructure. J Gen Physiol. 1967 Nov;50(10):2437–2458. doi: 10.1085/jgp.50.10.2437. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GINSBORG B. L. Spontaneous activity in muscle fibres of the chick. J Physiol. 1960 Mar;150:707–717. doi: 10.1113/jphysiol.1960.sp006413. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guth L., Watson P. K., Brown W. C. Effects of cross-reinnervation on some chemical properties of red and white muscles of rat and cat. Exp Neurol. 1968 Jan;20(1):52–69. doi: 10.1016/0014-4886(68)90124-6. [DOI] [PubMed] [Google Scholar]
- HESS A. Structural differences of fast and slow extrafusal muscle fibres and their nerve endings in chickens. J Physiol. 1961 Jul;157:221–231. doi: 10.1113/jphysiol.1961.sp006717. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hartree W., Hill A. V. The Specific Electrical Resistance of Frog's Muscle. Biochem J. 1921;15(3):379–382. doi: 10.1042/bj0150379. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hess A. The structure of vertebrate slow and twitch muscle fibers. Invest Ophthalmol. 1967 Jun;6(3):217–228. [PubMed] [Google Scholar]
- KATZ B., MILEDI R. FURTHER OBSERVATIONS ON THE DISTRIBUTION OF ACTYLCHOLINE-REACTIVE SITES IN SKELETAL MUSCLE. J Physiol. 1964 Mar;170:379–388. doi: 10.1113/jphysiol.1964.sp007338. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kiyohara T., Sato M. Membrane constants of red and white muscle fibers in the rat. Jpn J Physiol. 1967 Dec 15;17(6):720–725. doi: 10.2170/jjphysiol.17.720. [DOI] [PubMed] [Google Scholar]
- LOWY B. A., RAMOT B., LONDON I. M. Adenosine triphosphate metabolism in the rabbit erythrocyte in vivo. Nature. 1958 Feb 1;181(4605):324–326. doi: 10.1038/181324a0. [DOI] [PubMed] [Google Scholar]
- Mayr R. Zur elektronenmikroskopischen Unterscheidbarkeit eines einfach und eines multipel innervierten Hühnermuskels. Naturwissenschaften. 1967 Jan;54(1):22–22. doi: 10.1007/BF00608073. [DOI] [PubMed] [Google Scholar]
- SILVER A. A HISTOCHEMICAL INVESTIGATION OF CHOLINESTERASES AT NEUROMUSCULAR JUNCTIONS IN MAMMALIAN AND AVIAN MUSCLE. J Physiol. 1963 Nov;169:386–393. doi: 10.1113/jphysiol.1963.sp007263. [DOI] [PMC free article] [PubMed] [Google Scholar]
