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The effects of baclofen on the stretch reflex parameters of the cat

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Abstract

Experiments were done in cats decerebrated at the precollicular postmammillary level to determine how a tonic increase of presynaptic inhibition of the intraspinal terminals of muscle spindle afferents changes the mechanical properties of the soleus stretch reflex (s.r.). Baclofen, a specific GABAB receptor agonist, was injected i.v. (1–2 mg/kg) so as to induce a tonic increase in presynaptic inhibition. The effects of baclofen on the stiffness and threshold of the s.r. were determined, respectively, from plots of stiffness vs background force and force vs length (length-tension plot). Baclofen, at these doses, had no effect on the excitation-contraction coupling properties of muscle or on the intrinsic stiffness-force relation. Changes of the soleus background force, required to obtain the stiffness vs force plots, were produced by stimulation of the contralateral common peroneal nerve or the posterior tibial nerve and occasionally by electrical stimulation in the area of the red nucleus. The stiffness of the s.r. as a function of the background force level was determined by stretching the muscle with a square pulse of 1–2 mm amplitude and 200–300 ms duration. The stiffness at each force level was calculated by dividing the change in force by the change in length, at a point where the force trace had stabilized. The length-tension relation of the s.r. was determined by stretching the muscle 12–17 mm at a constant rate of 1–2 mm/s. At all force levels, baclofen produced a significant decrease (40% or more) in the s.r. stiffness, within 10–15 min of injection as determined from the stiffness-force plots. The length-tension plots revealed that the decrease of s.r. stiffness was always accompanied by an increase in the s.r. threshold (typically 2–3 mm). It is suggested, therefore, that the s.r. threshold is not an independent variable, depending on the membrane potential of the α- motoneurons, and additionally on the level of presynaptic inhibition of the muscle spindle afferent terminals. The present results also imply that it may be possible for the CNS to adaptively modify the s.r. stiffness via presynaptic inhibition of the intraspinal terminals of muscle afferents. However, any such change of s.r. stiffness will be accompanied by a change in the s.r. threshold.

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References

  • Berkinblit MB, Feldman AG, Fukson OI (1986) Adaptability of innate motor patterns and motor control mechanisms. Behav Brain Sci 9:585–638

    Google Scholar 

  • Bormann J (1988) Electrophysiology of GABAA and GABAB receptor subtypes. Trends Neurosci 11:112–116

    Google Scholar 

  • Brownstone RM, Jordan LM, Kriellaars DJ, Noga BR, Shefchyk SJ (1992) On the regulation of repetitive firing in lumbar motoneurones during fictive locomotion in the cat. Exp Brain Res 90:441–455

    Google Scholar 

  • Capaday C (1994) The effects of a tonic increase of presynaptic inhibition of muscle spindle afferents on the stretch reflex parameters of the cat. Soc Neurosci Abstr 20:1583

    Google Scholar 

  • Capaday C, Stein RB (1986) Variations of reflex parameters and their implications for the control of movements. Behav Brain Sci 9:600–601

    Google Scholar 

  • Capaday C, Stein RB (1987a) A method for simulating the reflex output of a motoneuron pool. J Neurosci Methods 21:91–104

    Article  CAS  Google Scholar 

  • Capaday C, Stein RB (1987b) Difference in the amplitude of the human soleus H-reflex during walking and running. J Physiol (Lond) 392:513–522

    Google Scholar 

  • Capaday C, Stein RB (1989) The effects of postsynaptic inhibition on the monosynaptic reflex of the cat at different levels of motoneuron pool activity. Exp Brain Res 77:577–584

    CAS  PubMed  Google Scholar 

  • Cedarbaum JM, Schleifer LS (1990) Drugs for Parkinsons's disease, spasticity, and acute muscle spasms. In: Goodman Gilman A, Rall TW, Nies AS, Taylor P (eds) The pharmacological basis of therapeutics. Pergamon Press, New York, pp 463–484

    Google Scholar 

  • Creed RSD, Denny-Brown D, Eccles JC, Liddell EGT, Sherrington C (1932) Reflex activity of the spinal cord. Oxford University Press, New York

    Google Scholar 

  • Eccles JC (1964) The physiology of synapses. Academic Press, New York

    Google Scholar 

  • Eccles JC, Kostyuk PG, Schmidt RF (1962) Central pathways responsible for depolarization of primary afferent fibers. J Physiol (Lond) 161:258–281

    Google Scholar 

  • Edwards FR, Harrison PJ, Jack JJB, Kullmann DM (1989) Reduction by baclofen of monosynaptic EPSPs in lumbosacral motoneurones of the anaesthetized cat. J Physiol (Lond) 416:539–556

    Google Scholar 

  • Fehr HU, Bein HJ (1974) Site of action of a new muscle relaxant (baclofen, Lioresal, Ciba 34 647-Ba). J Int Med Res 2:36–47

    Google Scholar 

  • Feldman AG, Orlovsky GN (1972) The influence of different descending systems on the tonic stretch reflex of the cat. Exp Neurol 37:481–494

    Google Scholar 

  • Granit R (1958) Neuromuscular interaction in postural tone of the cat's isometric soleus muscle. J Physiol (Lond) 143:387–402

    Google Scholar 

  • Henatsch HD, Student C, Student U, Takano K (1976) Controlled variations of input-output parameters affecting the active tension-extension diagram during muscle stretch. Prog Brain Res 44:403–412

    Google Scholar 

  • Hoffer JA, Andreassen S (1981) Regulation of soleus muscle stiffness in premammillary cats: intrinsic and reflex components. J Neurophysiol 45:267–285

    Google Scholar 

  • Hogan NJ (1984) Adaptive control of mechanical impedance by coactivation of antagonist muscles. IEEE Trans Automat Contr 29:681–690

    Google Scholar 

  • Houk JC (1978) Participation of reflex mechanisms and reaction time processess in the compensatory adjustments to mechanical disturbances. In: Desmedt JE (ed) Cerebral motor control in man: long loop mechanisms. Karger, Basel, pp 193–215

    Google Scholar 

  • Houk JC, Rymer WZ (1981) Neural control of muscle length and tension. In: Brooks VB (ed) The nervous system, vol II, Motor control. American Physiological Society, Bethesda, pp 257–233

    Google Scholar 

  • Hultborn H, Meunier S, Morin C, Pierrot-Deseilligny E (1987) Assessing changes in presynaptic inhibition of Ia fibres: a study in man and the cat. J Physiol (Lond) 389:729–756

    Google Scholar 

  • Jankowska E (1992) Interneuronal relay in spinal pathways from proprioceptors. Prog Neurobiology 38:335–378

    Google Scholar 

  • Jiménez I, Rudomin P, Enriquez M (1991) Differential effects of(-)baclofen on Ia and descending monosynaptic EPSPs. Exp Brain Res 85:103–113

    Google Scholar 

  • Kernell D, Hultborn H (1990) Synaptic effects on recruitment gain: a mechanism of importance for the input-output relations of motoneurone pools. Brain Res 507:176–179

    Google Scholar 

  • Lacquaniti F, Licata F, Soechting JF (1982) The mechanical behavior of the human forearm in response to transient perturbations. Biol Cybern 44:35–46

    Google Scholar 

  • Latash ML, Penn RD, Corcos DM, Gottlieb GL (1989) Short-term effects of intrathecal baclofen in spasticity. Exp Neurol 103:165–172

    Google Scholar 

  • Lavoie BA, Capaday C, Comeau F (1993) Presynaptic inhibition of Ia-afferent terminals during standing and walking in humans. Soc Neurosci Abstr 19:538

    Google Scholar 

  • Liddell EGT and Sherrington C (1924) Reflexes in response to stretch (myotatic reflexes). Proc R Soc Lond [Biol] 96:212–242

    Google Scholar 

  • Matthews PBC (1959a) The dependence of tension upon extension in the stretch reflex of the soleus muscle of the decerebrate cat. J Physiol (Lond) 147:521–546

    Google Scholar 

  • Matthews PBC (1959b) A study of certain factors influencing the stretch reflex of the decerebrate cat. J Physiol (Lond) 147:547–564

    Google Scholar 

  • Matthews PBC (1972) Mammalian muscle receptors and their central actions. Arnold, London

    Google Scholar 

  • Matthews PBC (1981) Evolving views on the internal operation and functional role of the muscle spindle. J Physiol (Lond) 320:1–30

    Google Scholar 

  • Meunier S, Pierrot-Deseilligny E (1989) Gating of the afferent volley of the monosynaptic stretch reflex during movement in man. J Physiol (Lond) 419:753–763

    Google Scholar 

  • Milner TE, Cloutier C (1993) Compensation for load instability: limits of joint stiffness. Soc Neurosci Abstr 19:992

    Google Scholar 

  • Morin C, Katz R, Mazières L, Pierrot-Deseilligny E (1982) Comparison of soleus H-reflex facilitation at the onset of soleus contractions produced voluntarily and during the stance phase of human gait. Neurosci Lett 33:47–53

    Google Scholar 

  • Nichols TR, Houk JC (1976) Improvement in linearity and regulation of stiffness that results from actions of the stretch reflex. J Neurophysiol 39:119–142

    Google Scholar 

  • Nichols TR, Sleeves JD (1986) Resetting of resultant stiffness in ankle flexor and extensor muscles in the decerebrate cat. Exp Brain Res 62:401–410

    Google Scholar 

  • Peng YY, Frank E (1989a) Activation of GABAB receptors causes presynaptic inhibition at synapses between muscle spindle afferents and motoneurons in the spinal cord of bullfrogs. J Neurosci 9:1502–1515

    Google Scholar 

  • Peng YY, Frank E (1989b) Activation of GABAA receptors causes presynaptic and postsynaptic inhibition at synapses between muscle spindle afferents and motoneurons in the spinal cord of bullfrogs. J Neurosci 9:1516–1522

    Google Scholar 

  • Pompeiano O (1960) Alpha types of release studied in tension-extension diagrams from cat's forelimb triceps muscle. Arch Ital Biol 98:92–117

    Google Scholar 

  • Powers RK, Campbell DL, Rymer WZ (1989) Stretch reflex dynamics in spastic elbow flexor muscles. Ann Neurol 25:32–42

    Google Scholar 

  • Rack PMH, Westbury DR (1974) The short range stiffness of active mammalian muscle and its effect on mechanical properties. J Physiol (Lond) 240:331–350

    Google Scholar 

  • Rudomin P (1990) Presynaptic inhibition of muscle spindle and tendon organ afferents in the mammalian spinal cord. Trends Neurosci 13:499–506

    Google Scholar 

  • Stein RB, Capaday C (1988) The modulation of human reflexes during functional motor tasks. Trends Neurosci. 11:328–332

    Google Scholar 

  • Stuart GJ, Redman SJ (1991) The role of GABAA and GABAB receptors in presynaptic inhibition of Ia EPSPs in cat spinal cord. J Physiol (Lond) 447:675–992

    Google Scholar 

  • Sypert GW, Munson JB (1984) Excitatory synapses. In: Davidoff RE (ed) Handbook of the spinal cord, vol 1, Physiology. Dekker, New York, pp 315–384

    Google Scholar 

  • Thilmann AF, Fellows SJ, Garms E (1991) The mechanism of spastic muscle hypertonus. Brain 114:233–244

    Google Scholar 

  • Zajac FE (1989) Muscle and tendon: properties, models, scaling, and application to biomechanics and motor control. Crit Rev Biomed Eng 17:359–411

    Google Scholar 

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Capaday, C. The effects of baclofen on the stretch reflex parameters of the cat. Exp Brain Res 104, 287–296 (1995). https://doi.org/10.1007/BF00242014

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