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

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.

[1]  N. Secher,et al.  Contralateral influence on recruitment of curarized muscle fibres during maximal voluntary extension of the legs. , 1978, Acta physiologica Scandinavica.

[2]  J. Poortmans,et al.  Metabolic Adaptation to Prolonged Physical Exercise , 1975 .

[3]  H. A. Padykula,et al.  THE SPECIFICITY OF THE HISTOCHEMICAL METHOD FOR ADENOSINE TRIPHOSPHATAS , 1955, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[4]  A. R. Lind,et al.  Circulatory responses to sustained hand‐grip contractions performed during other exercise, both rhythmic and static , 1967, The Journal of physiology.

[5]  J. Mitchell,et al.  Blood pressure and heart rate response to static exercise in relation to electromyographic activity and force development. , 1981, Acta physiologica Scandinavica.

[6]  N. Secher,et al.  Glycogen Depletion Pattern in Human Muscle Fiber During Work under Curarization (d-Tubocurarine) , 1975 .

[7]  D. McCloskey,et al.  Reflex cardiovascular and respiratory responses originating in exercising muscle , 1972, The Journal of physiology.

[8]  P. Jewell,et al.  A differentiation between red and white muscle in the cat based on responses to neuromuscular blocking agents , 1954, Journal of Physiology.

[9]  F. Smirk,et al.  Observations in man on a pulse‐accelerating reflex from the voluntary muscles of the legs , 1938, The Journal of physiology.

[10]  N. Secher,et al.  Effect of Tubocurarine on Human Soleus and Gastrocnemius Muscles , 1982, Acta anaesthesiologica Scandinavica.

[11]  F. Smirk,et al.  Observations in man upon a blood pressure raising reflex arising from the voluntary muscles , 1937, The Journal of physiology.

[12]  W. Paton,et al.  The action of d‐tubocurarine and of decamethonium on respiratory and other muscles in the cat , 1951, The Journal of physiology.

[13]  J. Mitchell,et al.  The exercise pressor reflex: its cardiovascular effects, afferent mechanisms, and central pathways. , 1983, Annual review of physiology.

[14]  S. Johansen,et al.  Endurance time in static work during partial curarization. , 1969, Journal of applied physiology.

[15]  E. Asmussen,et al.  On the Regulation of Circulation during Muscular Work. , 1943 .

[16]  P. Painter,et al.  Increased cardiovascular response to static contraction of larger muscle groups. , 1982, Journal of applied physiology: respiratory, environmental and exercise physiology.

[17]  G. Borg Perceived exertion as an indicator of somatic stress. , 2019, Scandinavian journal of rehabilitation medicine.

[18]  A Krogh,et al.  The regulation of respiration and circulation during the initial stages of muscular work , 1913, The Journal of physiology.

[19]  C. Borst,et al.  Cardiac acceleration elicited by voluntary muscle contractions of minimal duration. , 1972, Journal of applied physiology.

[20]  Motor end‐plate differences as a determining factor in the mode of action of neuromuscular blocking substances , 1953 .

[21]  E Hultman,et al.  Blood pressure and heart rate response to voluntary and nonvoluntary static exercise in man. , 1982, Acta physiologica Scandinavica.

[22]  A. Krogh,et al.  A comparison between voluntary and electrically induced muscular work in man , 1917, Journal of Physiology.

[23]  J. Mitchell,et al.  The role of muscle mass in the cardiovascular response to static contractions , 1980, The Journal of physiology.

[24]  A P Hollander,et al.  Cardiac acceleration in man elicited by a muscle-heart reflex. , 1975, Journal of applied physiology.

[25]  E. Asmussen,et al.  ON THE NERVOUS FACTORS CONTROLLING RESPIRATION AND CIRCULATION DURING EXERCISE. EXPERIMENTS WITH CURARIZATION. , 1965, Acta physiologica Scandinavica.