LATERAL CORD STIMULATION (LCS) TO RELIEVE SPASTICITY. EXPERIMENTAL PROTOCOL AND RESULTS

 

Andreani J.CM MD, Guma C MD

 

CAECIF (Centro Argentino de Estimulaciòn y Cirugìa Funcionales) – Buenos Aires - Argentina

jcmandreani@yahoo.com.ar

 


Abstract

This experiment demmonstrates lateral cord electrical stimulation producing increases in threshold to declenche abnormally propagated electromyographic evoked responses induced by electrical stimulation of 4th lumbar root in pigs with experimental cortical and sub-cortical lesion, its results, its physiopathogenical and therapeutical relations with spasticity.Cerebellar Electrical Stimulation sometimes has limited results as a treatment for spasticity accompanying Cerebral Palsy, because this stimulation can produce a mixture of excitatory and inhibitory impulses on Spinal Cord neural circuits of uncertain effects.The rationale of this research is to produce a more inhibitory and safer action by indirect cerebellar stimulation through Spino-cerebellar tracts on lateral cord surface avoiding collateral action produced by current electrical spreading on cerebellar surface.To demonstrate this hypothesis pigs with surgical unilateral cortical and sub-cortical brain damage were used. A double laminectomy, cervical (C3-C4) and lumbar (L3-L6) was made and thresholds for spasmogenic abnormal electromyographic responses, disseminated on adjacents segments, facilitated by spinal liberation, and produced by extradural electrical stimulation of 4th lumbar root, were measured before and after a lateral cord cervical stimulation.So, our studied variable is the minimal amount of current declenching electromyographic responses in far placed myotomes(L7).Results in ten animals show significant increase of threshold after Lateral Cord Stimulation (LCS).These findings allow extrapolate the transfer of results and propose LCS as a new tool to treat human spasticity.

1. INTRODUCTION

The use of cerebellar electrical stimulation by  CES surgical implant of neurostimulators to improve motor performance in spastic cerebral palsy and refractory epilepsy, was described by Cooper in 1972 (7), and is based on classical works of Moruzzi showing decrease of hypertony in decerebrate cats after feline cerebellar cortex stimulation at high frequency (17,18). Spinocerebellum is the main source of this inhibitory effect produced through deep nuclei and rubro-spinal tracts synapsing interneurons in the spinal cord (2,11,17,18,21, 22), through spinocerebellar tracts entering the cerebellum through superior and inferior cerebellar peduncle (9).Decrease of spinal extensor motoneuron reflexes following  paravermal cerebellar stimulation at high frequencies, was demmostrated (5). This system works as a constant feed-back signaling level of descending motor activity (3). The main part of this system starts in vermian surface and parasagital cortex, so stimulating electrodes are placed in those regions (8,10)  Inhibitory action of cerebellar cortex is mediated by Purkinje cells (25) and also volontary motor activity is shaped by Purkinje cells modulation(12,16,25). A good percentage of succes has been reported by CES (8),but it has seldom limited usefullness because of the mixture of inhibitory and excitatory influencies in reason of the intrincated cerebellar physiology and because of activation of excitatory cortex and sub-cortex (23). Good results and shortcomings have been shown in many centers, (8,14). Our proposal is try to avoid shortcomings and improve results by stimulating another point of the Spinocerebellar circuits by indirect way, via lateral spinal cord, by means of spino-cerebellar tracts. LCS could enhance the modulatory action of this system.

1.1. Investigation design

Our aim is to determine if mean thresholds necessary to declenhe abnormally propagated electromyographic responses, by 4th root stimulation, increases after LCS in relation to identical previous measures without LCS in surgically brain damaged pigs. We have employed a new animal model in pigs (see Andreani et al, poster, this meeting), with cortical and sub-cortical brain damage.This propagated reponse isn´t normally present under those parameters of stimulation (1,4,15), and they appear after a upper motor neuron lesion. Electrical parameters  for radicular stimulation were  adapted and both clinical (1) and experimental (20,24) methods were taken as models.  Pulses of 25Hz, with a duration of 100 microseg. p.p., employing  increasing units of 0,5 mA each one, were used.The rational of such an adaptation was to measure the threshold to declenche it in progressive measures.Our investigational design is a prospective, longitudinal, with related samples, and comparision experiment

2. MATERIALS AND METHODS

EMG records and  radicular stimulation were done with an equipment MEDELEC- model SINERGY, range 2,5 mvolts, sew EEP 50mseg, low frequency filter 50 hz, high frequency filter 1kj, monitor sensibility 200 microvolts, two chnnels, setup adquisition. Electrical parameters for lateral cord stimulation were those used for  Dosal Column Stimulation: 100microsec pp, 45 Hz, 8 volts  (MEDTRONIC– Neuroestimulador ITREL II – Mn Minessota USA) Ten  pigs were studied, weighting 30-40 kg , anesthesia with ketamine  clorhidrate was used by intravenous perfusion 50 mg per kilo. Twenty days after brain lesion , a double exposure cervical (C3-C4) and lumbar (L3-L7) was preformed to explore contralateral stroke side. Cervical spinal cord was exposed to place an electrode on its lateral surface. Two needle electrodes were placed in cuadriceps muscle supplied by 4th lumbar root, and in semitendinous  muscle innervated by 7th lumbar root for EMG record. left 4th lumbar root was localized by EMG recording on cuadriceps muscle.Once this root inividualized an electode was extra durally placed on it . Then, L4 root was stimulated with an increasing electrical amplitude of equal amount, lasting 0,5 sec each, 3 seconds, till a maximal EMG response was obtained in rectus anterioris mucle   (cuádriceps).This value was coded X0.A an identical set of electrical activation was again started from the value obtained in X0 with equal parameters, till  an interferencial EMG  response (also visible) was obtained in semitendinous muscle. This value was coded X1. This proceeding was repeated another 3 times, leaving a delay of 2,5 minutes among measures , and results were  coded   X2;  X3, y  X4. Next step was to perform a similar sequence of meas ures , but intermingling two minutes of lateral cord stimulation (LCS) in free-time among them, using an electrode Resumée TL cuadripolar – MR MEDTRONIC, adapted to deliver its charge on the top electrode disk for better discharge on the reduced surface of the lateral cord, and already described electrical parameters were applied. These values were coded X’0, X’1, X’2, X’3 and X’4. Sessions of LCS were  delivered between measures  X’0 – X’1;  X’1 – X’2;  and X’2 –X’3 ,but  not between  X’3 – X’4  to evaluate post-effect.

3. RESULTS

Mean values of  X´0 compared to X0 showed no stadistical differences.Measures of current spreading X’1 in relation to X1, X2 toX´2, X3 to X’3 and X4 to X’4 were sinificant (see table of results in figure1).

FIGURE 1

4. DISCUSSION AND CONCLUSIONS

Increases of mean electrical thresholds necessary to produce a maximal EMG response in our animal model, is the main fact in the present experiment. A post-effect in the last series of measures (X´4) was also noted confirming the validity of the method. In the whole measures we had observed a lesser amount of variation than observed for other authors (15, 19, 24). Increases of thresholds for propagated descharges to others spinal cord segments, seen after LCS, are, in our opinion, the result of electrical activation of the spinocerebellum by means of volleys of impulses travelling in the lateral cord and via  spino – cerebellar tracts, wich are superficially placed. Neither movements nor EMG responses on forelimbs during LCS were observed, then inhibitory action through pyramidal tract stimulation should be considered absent or accesory. Dorsal column stimulation by current spreading could also play an accessory roll on this inhibitory action, but it couldn’t be so marked on hindlimbs. LCS acting whatever way produces inhibition of those abnormal reflexes at spinal cord level, that were abnormally liberated by surgical upper motor experimental lesion.When CES was used as a treatment, by  radiofrequency linked systems, atrophy of cerebellar cortex and lost of efficacy for chronic use were seldom seen. Electrical current spread during direct cerebellar stimulation and tingling on the occiput was felt by patients when charge was about 25 – 30 micro C/sq.cm./ph (8). There was also a “window effect”, that meant lost of effects below 0,8 and over 5 microC/sq.cm./ph.(8) and potential tisular damage when current intensity rised(6).This current spreading can occur in absence of tingling sensation by Coulomb’s doctrine,producing undesirable neocerebellar activation. These shortcomings had been avoided with the use of new implantable stimulators and with correction of electrical charges delivered (8). LCS could be a different way to solve those problems. Direct stimulation of superior cerebellar peduncle by stereotaxic method (SCP) was tryied (13), requiring trained personal , high  thecnology, and has  a high cost.  Dorsal cord stimulation shows 53% of improvement with an electrical stimulation of 500 HZ, and better results with quadripolar systems are described (8), and better effect on arms and neck are seen.In these experiment increases in threshold necessary to produce abnormal activity, via LCS, has the sense of inhibitory action on abnormal motor system.It is more physiologic than direct stimulation of the cerebellum, the volley of afferent impulses on it, comes of a far-placed zone, so current spreading cannot affect whole cerebellar cortex, increasing modulatory efficency of the stimulation.Finally. The above exposed reasons let the author to postulate a new therapeutical method, by an implantable system, to produce LCS, to joint other therapeutical ressources for Spasticity.

REFERENCES

1) Abbot R: Electrical stimulation in selective dorsal rhizotomy .En :Electrical and Magnetic Stimulation of the Brain and Spinal Cord . Raven Press Ltd. New  York 1993 ; pp 263- 70.

2) Alstermark B, Lundberg A, Sarabi S, et al. Integration in descending motor pathways in the cat. Inhibition pathways to forelimbs motoneurons via C3-C4 propiospinal neurons.  Exp Brain Res 56: 279-292, 1984.

3) Arshavsky, Gelfand W I, Orlovsky G N, et al: Messages conveyed by spinocerebellar pathways during scratching in the cat. Activity of neurons in the lateral reticular nucleus. Brain Res 151:479-491, 1978

4) Barolat Romana G ; DavisR:Neurophysiological mechanisms in abnormal reflex activities in  cerebral palsy and spinal spasticity . J. Neurol. Neurosurg., and Psychiatry1980:219– 244

5) Bloedel JR, Ebner TJ, Godersky JC, et al.   Physiological mechanisms underlying the effects of cerebellar stimulation.  In Davis R,Bloedel JR, Editors.Cerebellar stimulation for spasticity and seizures.Boca Raton, FL, USA:CRC Press: 1984.

6) Brown W, Babb T, Soper H, et al.  Tissue reaction to long term electrical stimulation of the cerebellum in monkeys. J Neurosurg 1977;47:366.

7)Cooper  IS (PD): Cerebellar Stimulation in Man . New York, Raven Press 1978, p 222.

8) Davis  R :  Cerebellar stimulation for cerebral palsy, function and seizures . Arch. of Med. Res.  31 (2000) ; 290 – 9.

9) Delmas A : Voies et Centres Nerveux . Ed Masson- Paris 1981:p 148-150.

10)Dow RS ; Moruzzi G:The Physiology and Pathology of the cerebellum.

 Mineapolis,Mn.Universityof  MinnesotaPress, 1958

11) Fassano  VA ; Barolat G ; Teme S ; et al  : Electrophysiological assesment of spinal circuits in spasticity by direct dorsal root stimulation . Neurosurgery 4, 146 – 51 , 1979.

12) Fortier P.A, Kalaska  JF, Smith A. M.    Cerebellar neuronal activity related to whole – arm reaching movements in the monkey.                          J Neurophysiol 62: 198 – 211,1989.

13) Galanda M, Hovath S :  Different effects of chronic electrical stimulation and motor disorders . Stereotact Funct Neurosurg 1997, 69-116.

14) Hershler C; Upton AR; et al.:Effects of cerebellar stimulation on cerebral palsy in adults. Pace Pacing – Clin – Electrophysiol. 1989 May; 12 (5): 861 – 9.

15) Magladery JW ; Teasdall RD ; Plalsk M et al  : Electrophysiological studies of reflex activity in patients with lesions of the Central Nervous System . A comparision of a spinal motoneuron excitability following afferent nerve volleys in normal patients and patients with upper motor neuron lesions  Bulletin of John Hopkings Hospital 1952 ; 91 : 219 : 337.

16)Mano N, Yamamoto K.   Simple – spike activity of cerebellar Purkinje cells related to visually guided wrist traking movement in the monkey. J. Neurophysiol. 43: 713 – 728, 1980.

17) Moruzzi, G  : Effects at different frequencies of cerebellar stimulation upon postural tonus and reflexes . EEG Clin Neurophys 1950, 248.

18) Moruzzi G « Problems in cerebellar physiology . Ch Thomas 1950. Sprinfield III

19) Nishida T, Storrs BB. Electrophysiological monitoring in selective posterior rhizotomy for spasticity :  principles, technique and interpretation of responses. En Sindou M , Abbot R , Eds, Neurosurgery for spasticity. Wien: Spinger- Verlag ; 1991 : 159-164.

20) Phillips L H; Park TS : Electrophysiologic studies of selective posterior rhizotomy patients.  In Parks TS,  Phillips LH,  Peacock WJ (eds).  Manegement of Spasticity in Cerebral Palsy and Spinal Cord Injury:State of the Art Reviews Vol. 4 , N2. Ph: Hanley&Belfus,1989; pp459 – 69.

21) Pierrot Deseilligny E;Mazières L :Spinal Mechanisms underlying Spasticity. In Delwaide PJ,Young RP Eds: Clinical Neurophysiology in Spasticity.Amsterdam Elsevier1985:pp63-  76

22) Ratusnik DL ; Wolf VI ; Penn RD , et al : Effects on Speech of Chronic Cerebellar Stimulation in Cerebral Palsy. J. of Neurosurg ; 48 Jun 1978 : pp 876

23) Rispail P : Changes in Motor Responses induced by Cerebellar Stimulation during clasical forelimb flexion conditioning in the cat. Exp. Brain 28: pp 101- 123 Dec 1977.

24) Rivera A:An experimental study of reflex variability in Selective Dorsal Rhizotomy. J.Neurosurg. 81:pp885- 94 ; 1994.

25) Rosen I, Schieid P : Cerebellar surface cooling influencing evoked activity in cortex and interpositus nucleus. Brain Res 45 : 580-584, 1972.

Acknowledgdments:

The authors thank Dr E. Mele V D, for vetrinarian care, Dr N. Castiglia MD  for her statistical analysis, and to Miss Neri, Mr L Sanjurjo and Mr P Pomarada for his technical support and assistance.