Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1985 Feb;359:365–379. doi: 10.1113/jphysiol.1985.sp015590

Partial neuromuscular blockade and cardiovascular responses to static exercise in man.

B Leonard, J H Mitchell, M Mizuno, N Rube, B Saltin, N H Secher
PMCID: PMC1193380  PMID: 3999043

Abstract

In human subjects sustained static contractions of the quadriceps femoris in one leg were performed with the same absolute and the same relative intensity before and after partial neuromuscular blockade with either decamethonium or tubocurarine which reduced strength to about 50% of the control value. During the contractions performed with the same absolute force, the magnitude of the cardiovascular responses (heart rate and blood pressure) was greater during neuromuscular blockade than during control contractions. During the contractions involving the same relative force the magnitude of the cardiovascular responses was almost the same with and without neuromuscular blockade. These findings were independent of the drug used. The metabolic part of the exercise pressor reflex was assessed by the application of an arterial cuff 1/2 min before cessation of exercise and for the following 3 min of rest. Although heart rate and blood pressure decreased after cessation of exercise, application of the tourniquet resulted in higher post-exercise values and this effect was seen both with and without neuromuscular blockade. Muscle biopsies from the subjects' m. vastus lateralis were analysed for fast- and slow-twitch fibre composition showing 27-66% slow-twitch fibres. No correlation was found between cardiovascular responses to static exercise, with or without neuromuscular blockade, and fibre type predominance. The results suggest that the involvement of fast- or slow-twitch muscle fibres does not play a dominant role in the cardiovascular responses to static exercise in man. Both central command and reflex neural mechanisms are of importance, and it appears that these two control mechanisms are redundant and that neural occlusion may be operative. However, when partial neuromuscular blockade induces a disproportion between an increase in central command and a constant or decreasing muscle tension and metabolism, the larger signal arising from central command determines the magnitude of the cardiovascular responses.

Full text

PDF
365

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ASMUSSEN E., JOHANSEN S. H., JORGENSEN M., NIELSEN M. ON THE NERVOUS FACTORS CONTROLLING RESPIRATION AND CIRCULATION DURING EXERCISE. EXPERIMENTS WITH CURARIZATION. Acta Physiol Scand. 1965 Mar;63:343–350. doi: 10.1111/j.1748-1716.1965.tb04073.x. [DOI] [PubMed] [Google Scholar]
  2. Alam M., Smirk F. H. Observations in man on a pulse-accelerating reflex from the voluntary muscles of the legs. J Physiol. 1938 Mar 14;92(2):167–177. doi: 10.1113/jphysiol.1938.sp003592. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Alam M., Smirk F. H. Observations in man upon a blood pressure raising reflex arising from the voluntary muscles. J Physiol. 1937 Jun 3;89(4):372–383. doi: 10.1113/jphysiol.1937.sp003485. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Borg G. Perceived exertion as an indicator of somatic stress. Scand J Rehabil Med. 1970;2(2):92–98. [PubMed] [Google Scholar]
  5. Borst C., Hollander A. P., Bouman L. N. Cardiac acceleration elicited by voluntary muscle contractions of minimal duration. J Appl Physiol. 1972 Jan;32(1):70–77. doi: 10.1152/jappl.1972.32.1.70. [DOI] [PubMed] [Google Scholar]
  6. Freyschuss U. Cardiovascular adjustment to somatomotor activation. The elicitation of increments in heart rate, aortic pressure and venomotor tone with the initiation of muscle contraction. Acta Physiol Scand Suppl. 1970;342:1–63. [PubMed] [Google Scholar]
  7. Goodwin G. M., McCloskey D. I., Mitchell J. H. Cardiovascular and respiratory responses to changes in central command during isometric exercise at constant muscle tension. J Physiol. 1972 Oct;226(1):173–190. doi: 10.1113/jphysiol.1972.sp009979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hollander A. P., Bouman L. N. Cardiac acceleration in man elicited by a muscle-heart reflex. J Appl Physiol. 1975 Feb;38(2):272–278. doi: 10.1152/jappl.1975.38.2.272. [DOI] [PubMed] [Google Scholar]
  9. Hultman E., Sjöholm H. Blood pressure and heart rate response to voluntary and nonvoluntary static exercise in man. Acta Physiol Scand. 1982 Aug;115(4):499–501. doi: 10.1111/j.1748-1716.1982.tb07110.x. [DOI] [PubMed] [Google Scholar]
  10. JEWELL P. A., ZAIMIS E. J. A differentiation between red and white muscle in the cat based on responses to neuromuscular blocking agents. J Physiol. 1954 Jun 28;124(3):417–428. doi: 10.1113/jphysiol.1954.sp005118. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Juhlin-Dannfelt A., Frisk-Holmberg M., Karlsson J., Tesch P. Central and peripheral circulation in relation to muscle-fibre composition in normo- and hyper-tensive man. Clin Sci (Lond) 1979 Apr;56(4):335–340. doi: 10.1042/cs0560335. [DOI] [PubMed] [Google Scholar]
  12. Krogh A., Lindhard J. A comparison between voluntary and electrically induced muscular work in man. J Physiol. 1917 Jul 3;51(3):182–201. doi: 10.1113/jphysiol.1917.sp001795. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Krogh A., Lindhard J. The regulation of respiration and circulation during the initial stages of muscular work. J Physiol. 1913 Oct 17;47(1-2):112–136. doi: 10.1113/jphysiol.1913.sp001616. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Lind A. R., McNicol G. W. Circulatory responses to sustained hand-grip contractions performed during other exercise, both rhythmic and static. J Physiol. 1967 Oct;192(3):595–607. doi: 10.1113/jphysiol.1967.sp008319. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. McCloskey D. I., Mitchell J. H. Reflex cardiovascular and respiratory responses originating in exercising muscle. J Physiol. 1972 Jul;224(1):173–186. doi: 10.1113/jphysiol.1972.sp009887. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Mitchell J. H., Kaufman M. P., Iwamoto G. A. The exercise pressor reflex: its cardiovascular effects, afferent mechanisms, and central pathways. Annu Rev Physiol. 1983;45:229–242. doi: 10.1146/annurev.ph.45.030183.001305. [DOI] [PubMed] [Google Scholar]
  17. Mitchell J. H., Payne F. C., Saltin B., Schibye B. The role of muscle mass in the cardiovascular response to static contractions. J Physiol. 1980 Dec;309:45–54. doi: 10.1113/jphysiol.1980.sp013492. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Molbech S., Johansen S. H. Endurance time in static work during partial curarization. J Appl Physiol. 1969 Jul;27(1):44–48. doi: 10.1152/jappl.1969.27.1.44. [DOI] [PubMed] [Google Scholar]
  19. OCHWADT B., BUECHERL E., KREUZER H., LOESCHCKE H. H. [Modification of respiratory increase in muscular work by partial neuromuscular block (tubocurarine)]. Pflugers Arch Gesamte Physiol Menschen Tiere. 1959;269:613–621. [PubMed] [Google Scholar]
  20. PADYKULA H. A., HERMAN E. The specificity of the histochemical method for adenosine triphosphatase. J Histochem Cytochem. 1955 May;3(3):170–195. doi: 10.1177/3.3.170. [DOI] [PubMed] [Google Scholar]
  21. PATON W. D. M., ZAIMIS E. J. The action of d-tubocurarine and of decamethonium on respiratory and other muscles in the cat. J Physiol. 1951 Feb;112(3-4):311–331. doi: 10.1113/jphysiol.1951.sp004531. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Petrofsky J. S., Lind A. R. The blood pressure response during isometric exercise in fast and slow twitch skeletal muscle in the cat. Eur J Appl Physiol Occup Physiol. 1980;44(3):223–230. doi: 10.1007/BF00421621. [DOI] [PubMed] [Google Scholar]
  23. Schibye B., Mitchell J. H., Payne F. C., Saltin B. Blood pressure and heart rate response to static exercise in relation to electromyographic activity and force development. Acta Physiol Scand. 1981 Sep;113(1):61–66. doi: 10.1111/j.1748-1716.1981.tb06862.x. [DOI] [PubMed] [Google Scholar]
  24. Seals D. R., Washburn R. A., Hanson P. G., Painter P. L., Nagle F. J. Increased cardiovascular response to static contraction of larger muscle groups. J Appl Physiol Respir Environ Exerc Physiol. 1983 Feb;54(2):434–437. doi: 10.1152/jappl.1983.54.2.434. [DOI] [PubMed] [Google Scholar]
  25. Secher N. H., Rube N., Secher O. Effect of tubocurarine on human soleus and gastrocnemius muscles. Acta Anaesthesiol Scand. 1982 Jun;26(3):231–234. doi: 10.1111/j.1399-6576.1982.tb01760.x. [DOI] [PubMed] [Google Scholar]
  26. Secher N. H., Rørsgaard S., Secher O. Contralateral influence on recruitment of curarized muscle fibres during maximal voluntary extension of the legs. Acta Physiol Scand. 1978 Aug;103(4):456–462. doi: 10.1111/j.1748-1716.1978.tb06240.x. [DOI] [PubMed] [Google Scholar]
  27. Warmolts J. R., Engel W. K. Open-biopsy electromyography. I. Correlation of motor unit behavior with histochemical muscle fiber type in human limb muscle. Arch Neurol. 1972 Dec;27(6):512–517. doi: 10.1001/archneur.1972.00490180048011. [DOI] [PubMed] [Google Scholar]
  28. ZAIMIS E. J. Motor end-plate differences as a determining factor in the mode of action of neuromuscular blocking substances. J Physiol. 1953 Nov 28;122(2):238–251. doi: 10.1113/jphysiol.1953.sp004995. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Physiology are provided here courtesy of The Physiological Society

RESOURCES