DETRUSOR-SPHINCTERIC DYSSYNERGIA IN HUMANS WITH SPINAL-CORD LESIONS MAY BE CAUSED BY A LOSS OF STABLE PHASE-RELATIONS BETWEEN AND WITHIN OSCILLATORY FIRING NEURONAL NETWORKS OF THE SACRAL MICTURITION CENTER

Citation
G. Schalow et al., DETRUSOR-SPHINCTERIC DYSSYNERGIA IN HUMANS WITH SPINAL-CORD LESIONS MAY BE CAUSED BY A LOSS OF STABLE PHASE-RELATIONS BETWEEN AND WITHIN OSCILLATORY FIRING NEURONAL NETWORKS OF THE SACRAL MICTURITION CENTER, Journal of the autonomic nervous system, 52(2-3), 1995, pp. 181-202
Citations number
46
Categorie Soggetti
Neurosciences
ISSN journal
01651838
Volume
52
Issue
2-3
Year of publication
1995
Pages
181 - 202
Database
ISI
SICI code
0165-1838(1995)52:2-3<181:DDIHWS>2.0.ZU;2-C
Abstract
(1) Single-fibre action potentials (APs) were recorded with 2 pairs of wire electrodes from lower sacral nerve roots during surgery in patie nts with spinal cord lesions and in a brain-dead human. Conduction vel ocity distribution histograms were constructed for afferent and effere nt fibres, nerve fibre groups were identified and simultaneous impulse patterns of alpha and gamma-motoneurons and secondary muscle spindle afferents (SP2) were constructed. Temporal relations between afferent and efferent APs were analysed by interspike interval (II) and phase r elation changes. (2) In a paraplegic with hyperreflexia of the bladder , urinary bladder stretch (S1) and tension receptor afferents (ST) fir ed already when the bladder was empty, and showed a several times high er bladder afferent activity increase upon retrograde bladder filling than observed in the brain-dead individual. Two alpha(2)-motoneurons ( FR) innervating the external bladder sphincter were already oscillator y firing to generate high activity levels when the bladder was empty. They showed activity levels with no bladder filling, comparable to tho se measured at a bladder filling of 600 ml in the brain-dead individua l. A bladder storage volume of 600 ml was thus lost in the paraplegic, due to a too high bladder afferent input to the sacral micturition ce nter, secondary to inflammation and hypertrophy of the detrusor. (3) I n a brain-dead human, 2 phase relations existed per oscillation period of 160 ms between the APs of a sphincteric oscillatory firing alpha(2 )-motoneuron, a dynamic fusimotor and a secondary muscle spindle affer ent fibre. Following stimulation of mainly somatic afferent fibres, th e phase relations changed only little. (4) In a paraplegic with dyssyn ergia of the urinary bladder also 2 phase relations existed per oscill ation period of 110 ms in a functional unit between the APs of a sphin cteric alpha-motoneuron, a fusimotor and a secondary spindle afferent fibre. The phase relations changed with time following stimulation of mainly somatic afferents. A second functional unit organized by phase- related interactions was phase related to the first functional unit. ( 5) Following painful bladder catheter pulling, the parasympathetic div ision was transiently activated several times in the paraplegic. At ti mes of activation of the parasympathetic division, 3 broad phase relat ions occurred within and between the two functional units, indicating that the parasympathetic division in the sacral micturition and defeca tion center channeled an additional input to the somatic oscillatory f iring neuronal networks driving motoneurons which innervate the extern al bladder and/or anal sphincters. (6) It is discussed that the parasy mpathetic division, activated physiologically for detrusor contraction , may have failed to inhibit the somatic neuronal network driving the external sphincters (detrusor-sphincteric dyssynergia), because the os cillatory firing somatic neuronal networks escaped from the inhibitory action by changing their phase relations of organization. (7) It is c onceivable that the mutual inhibitory action of detrusor and external bladder sphincter has the capacity to recover, if the functional neuro nal organization of the sacral micturition center is improved in the d irection of more stable oscillatory firing neuronal networks by natura l afferent inputs from continence organs and supraspinal neurons. For supraspinal control and improvement of neuronal organization some kind of bulbo-spinal-bulbo pathways have to exist or to be reconstructed. (8) In the clinical implications section a case is introduced in which a tetraplegic was made running again by training different spinal pat tern generators.