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. 1996 Aug 15;495(Pt 1):247–254. doi: 10.1113/jphysiol.1996.sp021589

Rostrocaudal gradient of electrical activation in the parasternal intercostal muscles of the dog.

A Legrand 1, A Brancatisano 1, M Decramer 1, A De Troyer 1
PMCID: PMC1160740  PMID: 8866367

Abstract

1. Because the inspiratory mechanical advantage of the canine parasternal intercostal muscles is greatest in the third interspace and decreases gradually in the caudal direction, the electromyograms of these muscles in interspaces 3, 5 and 7 have been recorded in anaesthetized, spontaneously breathing dogs. Each activity was expressed as a percentage of the activity measured during tetanic, supramaximal stimulation of the internal intercostal nerve (maximal activity). 2. Parasternal inspiratory activity during resting, room air breathing was invariably greater in the third than in the fifth interspace (62.0 +/- 6.0 vs. 41.3 +/- 4.6% of maximal activity; P < 0.001) and smallest in the seventh interspace (22.8 +/- 2.7% of maximal activity; P < 0.001). This distribution of activity persisted during hyperoxic hypercapnia and during breathing against increased inspiratory airflow resistance. 3. This rostrocaudal distribution of activity also persisted after complete paralysis of the diaphragm as well as after deafferentation of the ribcage. 4. Studies of the distribution of the muscle fibre types indicated that the parasternal intercostals in all interspaces had a higher proportion of slow-twitch oxidative (SO; type I) fibres than fast-twitch oxidative-glycolytic (FOG; type II a) fibres. 5. Thus the topographic distribution of parasternal inspiratory activity along the rostrocaudal axis of the ribcage is precisely matched with the topographic distribution of mechanical advantage. This extraordinarily effective pattern of activation probably results from the unequal distribution of central inputs throughout the parasternal motoneurone pool.

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Selected References

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  1. Brancatisano A., Amis T. C., Tully A., Engel L. A. Blood flow distribution within the rib cage muscles. J Appl Physiol (1985) 1991 Jun;70(6):2559–2565. doi: 10.1152/jappl.1991.70.6.2559. [DOI] [PubMed] [Google Scholar]
  2. De Troyer A., Legrand A. Inhomogeneous activation of the parasternal intercostals during breathing. J Appl Physiol (1985) 1995 Jul;79(1):55–62. doi: 10.1152/jappl.1995.79.1.55. [DOI] [PubMed] [Google Scholar]
  3. De Troyer A., Legrand A., Wilson T. A. Rostrocaudal gradient of mechanical advantage in the parasternal intercostal muscles of the dog. J Physiol. 1996 Aug 15;495(Pt 1):239–246. doi: 10.1113/jphysiol.1996.sp021588. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. De Troyer A., Ninane V. Triangularis sterni: a primary muscle of breathing in the dog. J Appl Physiol (1985) 1986 Jan;60(1):14–21. doi: 10.1152/jappl.1986.60.1.14. [DOI] [PubMed] [Google Scholar]
  5. De Troyer A., Yuehua C. Intercostal muscle compensation for parasternal paralysis in the dog: central and proprioceptive mechanisms. J Physiol. 1994 Aug 15;479(Pt 1):149–157. doi: 10.1113/jphysiol.1994.sp020284. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. ECCLES R. M., SEARS T. A., SHEALY C. N. Intra-cellular recording from respiratory motoneurones of the thoracic spinal cord of the cat. Nature. 1962 Mar 3;193:844–846. doi: 10.1038/193844a0. [DOI] [PubMed] [Google Scholar]
  7. Greer J. J., Martin T. P. Distribution of muscle fiber types and EMG activity in cat intercostal muscles. J Appl Physiol (1985) 1990 Oct;69(4):1208–1211. doi: 10.1152/jappl.1990.69.4.1208. [DOI] [PubMed] [Google Scholar]
  8. Loring S. H., Mead J. Action of the diaphragm on the rib cage inferred from a force-balance analysis. J Appl Physiol Respir Environ Exerc Physiol. 1982 Sep;53(3):756–760. doi: 10.1152/jappl.1982.53.3.756. [DOI] [PubMed] [Google Scholar]
  9. Mizuno M., Secher N. H. Histochemical characteristics of human expiratory and inspiratory intercostal muscles. J Appl Physiol (1985) 1989 Aug;67(2):592–598. doi: 10.1152/jappl.1989.67.2.592. [DOI] [PubMed] [Google Scholar]
  10. Reid M. B., Ericson G. C., Feldman H. A., Johnson R. L., Jr Fiber types and fiber diameters in canine respiratory muscles. J Appl Physiol (1985) 1987 Apr;62(4):1705–1712. doi: 10.1152/jappl.1987.62.4.1705. [DOI] [PubMed] [Google Scholar]
  11. Rochester D. F., Bettini G. Diaphragmatic blood flow and energy expenditure in the dog. Effects of inspiratory airflow resistance and hypercapnia. J Clin Invest. 1976 Mar;57(3):661–672. doi: 10.1172/JCI108322. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. SEARS T. A. THE SLOW POTENTIALS OF THORACIC RESPIRATORY MOTONEURONES AND THEIR RELATION TO BREATHING. J Physiol. 1964 Dec;175:404–424. doi: 10.1113/jphysiol.1964.sp007524. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. TAYLOR A. The contribution of the intercostal muscles to the effort of respiration in man. J Physiol. 1960 May;151:390–402. doi: 10.1113/jphysiol.1960.sp006446. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. van Lunteren E., Cherniack N. S. Electrical and mechanical activity of respiratory muscles during hypercapnia. J Appl Physiol (1985) 1986 Aug;61(2):719–727. doi: 10.1152/jappl.1986.61.2.719. [DOI] [PubMed] [Google Scholar]

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