Effects of adrenergic agents on the ventral horn cells in spinal cord slices isolated from adult rats

Effects of adrenergic agents on the ventral horn cells in spinal cord slices isolated from adult rats

$83 18. Motor system I. Spinal cord and proprioceptors EFFECTS ISOLATED OF A D R E N E R G I C AGENTS FROM ADULT RATS ON THE V E N T R A L HORN CE...

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$83

18. Motor system I. Spinal cord and proprioceptors EFFECTS ISOLATED

OF A D R E N E R G I C AGENTS FROM ADULT RATS

ON THE V E N T R A L

HORN CELLS

IN

SPINAL

CORD

SLICES

TAKASHI HIRAYAMA*, HIDEKI ONO and HIDEOMI FUKUDA, Department of T o x i c o l o g y and Pharmacology, Faculty of P h a r m a c e u t i c a l Sciences, The U n i v e r s i t y of Tokyo, Hongo, Bunkyo-ku, Tokyo 113, J a p a n The e x i s t e n c e of n o r a d r e n e r g i c fibers o r i g i n a t i n g in the b r a i n stem nuclei and terminating in both dorsal and ventral horns of the spinal cord is well known. However, r e g u l a t i n g m e c h a n i s m s of the spinal motor function through a d r e n o c e p t o r s are not yet elucidated. In this experiment, the effects of a d r e n o c e p t o r agonists and antagonists on synaptic activities of the ventral horn neurons were investigated using spinal cord slices. The slice p r e p a r a t i o n (400-450 ~m) was prepared from the lumbar e n l a r g e m e n t (L4-L5) of the spinal cord isolated from adult rats (9-10 weeks) under urethane (ig/kg,i.p.) and ~-chloralose (25mg/kg,i.p.) anesthesia. An action potential driven trans-synaptically following stimulation of the motor nuclei of the ventral horn was recorded extracellularly from the area close to the stimulating electrode. When a stimulus intensity with a low p r o b a b i l i t y for cellular d i s c h a r g e induction (less than 2/10) was used, norepinephrine (NE) caused a concentration-dependent increase in the p r o b a b i l i t y of firing. The f a c i l i t a t i o n produced by NE was b l o c k e d by the ~ l - a d r e n o c e p t o r antagonist, p r a z o s i n but not by the B - a d r e n o c e p t o r antagonist, propranolol or ~ 2 - a d r e n o c e p t o r antagonist, yohimbine. When a stimulus intensity that c o n s i s t e n t l y induced an action potential (10/10) was used, NE had no effect alone yet d e c r e a s e d the p r o b a b i l i t y of firing in the presence of prazosin. The inhibitory effect produced by NE was a n t a g o n i z e d by yohimbine. Selective ~ l - a d r e n o c e p t o r agonists (phenylephrine and methoxamine) increased the p r o b a b i l i t y of cellular discharge. C l o n i d i n e had similar effects to those of NE. These results c o n f i r m e d that the f a c i l i t a t i o n and inhibition of neuronal a c t i v i t i e s p r o d u c e d by NE are m e d i a t e d through ~ i - and e 2 - a d r e n o c e p t o r s , respectively. Facilitatory actions through ~ l - a d r e n o c e p £ o r s may play a dominant role in the adrenergic t r a n s m i s s i o n in the motor nuclei of the ventral horn.

M O D U L A T I O N OF REFLEX RESPONSES F I C T I V E L O C O M O T I O N IN THE CAT MITSUYO TSUKUBA

OF E L B O W F L E X O R

MOTONEURONS

H I S H I N U M A * AND TAKASHI YAMAGUCHI*, INSTITUTE UNIVERSITY, TSUKUBA, IBARAKI 305, J A P A N

DURING

FORELIMB

OF BASIC M E D I C A L

SCIENCES,

In order to examine the synaptic linkage b e t w e e n the forelimb locomotor p a t t e r n g e n e r a t o r and spinal reflex pathways, reflex responses to m u s c l e and skin a f f e r e n t s t i m u l a t i o n were i n t r a c e l l u l a r l y recorded from flexor m o t o n e u r o n s (brachialis, Br) during fictive locomotion, evoked by s t i m u l a t i o n of the m e s e n c e p h a l i c locomotor r e g i o n (MLR) in immobilized d e c e r e b r a t e cats w i t h the lower thoracic cord transected. Before M L R s t i m u l a t i o n (control stage), afferent v o l l e y s in deep and superficial radial nerves (DR and SR, muscle and skin nerves, respectively) p r o d u c e d large, late p o l y s y n a p t i c EPSPs (segmental latency more than 3 msec) in Br motoneurons. Further, Br m o t o n e u r o n s received early EPSPs (segmental latencies shorter than 2.5 msec) from DR nerves. When M L R s t i m u l a t i o n started, prior to a c t i v a t i o n of fictive locomotion, Br m o t o n e u r o n s h y p e r p o l a r i z e d and the late EPSPs were r e m a r k a b l y suppressed (80% or more). However, the early EPSPs were not suppressed as m u c h (20% or less). Thus, s u p p r e s s i o n of the polysynaptic, late EPSPs is p r e s u m a b l y not due to a c o n d u c t a n c e increase of m o t o n e u r o n s o c c u r r i n g w i t h h y p e r p o l a r i z a t i o n , but rather to inhibition or d i s f a c i l i t a t i o n of interneurons. During fictive locomotion, reflex r e s p o n s e s were p h a s e - d e p e n d e n t . In the e x t e n s o r - a c t i v e phase, the reflex r e s p o n s e s were suppressed as above. In the f l e x o r - a c t i v e phase, the early EPSPs from DR and the late EPSPs from SR recovered; the former i n c r e a s e d r e m a r k a b l y in m a g n i t u d e (more than twice the control) w h i l e the latter only o c c a s i o n a l l y exceeded those of the control. The late EPSPs from DR were still inhibited. Thus, it was suggested that reflex pathways m e d i a t i n g early EPSPs from muscle a f f e r e n t s and late EPSPs from skin a f f e r e n t s are facilitated by the locomotor p a t t e r n generator, e s p e c i a l l y the f l e x i o n - g e n e r a t i n g part.