Metabolic and neuroanatomical correlates of barrel-rolling and oculoclonic convulsions induced by intraventricular endothelin-1 : a novel peptidergic signaling mechanism in visuovestibular and oculomotor regulation ?

• Published in: Experimental brain research Vol. 95; no. 3; pp. 397 - 408
• Main Authors: GROSS, P. M, BENINGER, R. J, SHAVER, S. W, WAINMAN, D. S, ESPINOSA, F. J, WEAVER, D. F
• Format: Journal Article
• Language: English
• Published: Berlin Springer 01-08-1993
• Subjects: Animals; Autoradiography; Behavior, Animal - drug effects; Biological and medical sciences; Brain Chemistry - drug effects; Calcium Channels - drug effects; Endothelins - administration & dosage; Endothelins - pharmacology; Fundamental and applied biological sciences. Psychology; Glucose - metabolism; Histocytochemistry; Injections, Intraventricular; Male; Motor control and motor pathways. Reflexes. Control centers of vegetative functions. Vestibular system and equilibration; Nimodipine - pharmacology; Oculomotor Muscles - drug effects; Rats; Rats, Sprague-Dawley; Seizures - chemically induced; Seizures - metabolism; Seizures - pathology; Signal Transduction - drug effects; Vertebrates: nervous system and sense organs; Vestibular Nuclei - drug effects; Vestibular Nuclei - metabolism; Vision, Ocular - drug effects; Ocular motor pathway; Energy metabolism; Calcium; Rat; Rodentia; Central nervous system; Ionic channel; Endothelin 1; Glucose; Neuropeptide; Vertebrata; Mammalia; Convulsion; Intracerebral administration; Vestibular pathway; Visual vestibular integration; Brain (vertebrata)
• ISSN: 0014-4819; 1432-1106
• DOI: 10.1007/BF00227132

The neuroactive peptide endothelin-1 has receptors distributed abundantly among subdivisions and nuclei of the visuovestibular and oculomotor systems. In previous work, we and others described the convulsive manifestations resulting from central injection of this neuropeptide, including nystagmus, oculoclonus, exophthalmos, tonic hindlimb extension, and a generalized repetitive motor disturbance called barrel-rolling. We applied the quantitative, autoradiographic [14C]deoxyglucose method to examine the hypothesis that visuovestibular and oculomotor structures would become metabolically stimulated when endothelin was introduced into the brain via the ventricular system in conscious rats. Since previous work had demonstrated that hypermetabolic responses to endothelin in other neural systems were inhibited by an antagonist of neuronal calcium L-type channels, nimodipine, we further tested whether the increased function of vestibulooculomotor nuclei whose metabolic activity was sensitive to endothelin could be altered following nimodipine pretreatment via the ventricle. A single unilateral injection of endothelin (9 pmol in 3 microliters saline) into a lateral ventricle provoked significantly increased rates of glucose metabolism in 22 of 39 individual anatomical structures of the visuovestibular and oculomotor systems. Among those affected were the superficial stratum of the caudal superior colliculus (+25%), the optic tract bilaterally (+35 to 43%), the oculomotor cranial nerve nuclei (III, IV, VI; range of +21 to 47%), and the medial terminal nucleus of the accessory optic tract which harbors dense fields of endothelin binding sites (bilateral increase of +70 to 96%). Several other nuclei involved in the proprioceptive and visuovestibular disturbance caused by endothelin displayed increased metabolic activity, including the cuneate, gracile, sensory trigeminal, and prepositus hypoglossal nuclei, the vestibular subnuclear system, and the cerebellar flocculus. Identification of hypermetabolic responsivity to endothelin in these structures provides further information on the anatomical substrates mediating the behavioral phenomenology of endothelin-induced motor convulsions which involve the paroxysmal participation of the extraocular muscles and motor control systems producing barrel-rolling convulsions. Nimodipine pretreatment inhibited both the convulsive activity and the cerebral hypermetabolic responses to intraventricular endothelin. The results indicate that the neural systems sensitive to intraventricular endothelin become functionally active via a calcium-mediated process that may involve the neuropeptide as an intrinsic signaling molecule.