Plasticity in reflex pathways controlling stepping in the cat

被引:58
作者
Whelan, PJ [1 ]
Pearson, KG [1 ]
机构
[1] UNIV ALBERTA, DEPT PHYSIOL, EDMONTON, AB T6G 2H7, CANADA
关键词
D O I
10.1152/jn.1997.78.3.1643
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Previous studies have shown that stimulation of group 'I' afferents from ankle extensor muscles can prolong the cycle period in decerebrate walking cats and that the magnitude of these effects can be altered after chronic axotomy of the lateral-gastrocnemius/soleus (LGS) nerve. The effectiveness of LGS group I afferents in prolonging the cycle period decreases after axotomy, whereas the effectiveness of the uncut medial-gastrocnemius (MG) group I afferents is increased. The objectives of this investigation were to establish the time course of these changes in effectiveness and to determine whether these changes persist after transection of the spinal cord. The effects of stimulating the LGS and/or MG group I afferents on the cycle period were examined in 22 walking decerebrate animals in which one LGS nerve had been cut for 2 to 31 days. The effectiveness of LGS group I afferents declined progressively in the postaxotomy period, beginning with significant decreases at 3 days and ending close to zero effectiveness at 31 days. Large increases in the effectiveness of MG group I afferents occurred 5 days after axotomy, but there was no progressive change from 5 to 31 days. To test whether these changes in effectiveness were localized to sites within the spinal cord, the cord was transected in some decerebrate animals and stepping induced by the administration of L-DOPA L-3-4 dihydroxyphenylalanine (L-DOPA) and Nialamide. The effects of stimulating the MG and/or the LGS group I afferents on the cycle period were reexamined. In all four animals tested, stimulating the axotomized LGS group I afferents had a reduced effectiveness during locomotor activity in both the decerebrate and spinal states, whereas the increased effectiveness of the MG group I afferents was retained after transection of the spinal cord in two of five animals. Different mechanisms may be responsible for the changes in strength of the LGS and MG group I afferent pathways that project onto the rhythm generating sites in the spinal cord. This possibility follows from our observations of a linear relationship between the time after axotomy and decreased effectiveness of LGS group I afferents but no significant relationship between time postaxotomy and increased effectiveness of MG group I afferents; no significant relationship between the decreased effectiveness of LGS group I afferents and the increased effectiveness of MG group I afferents; and, after spinalization, consistent (4/4 cases) preservation of decreased LGS effectiveness but frequent (3/5 cases) loss of increased MG effectiveness.
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收藏
页码:1643 / 1650
页数:8
相关论文
共 31 条
[1]  
Baldissera F, 1981, HDB PHYSL 1 1, VII, P509, DOI DOI 10.1002/CPHY.CP010212
[2]  
BLOEDEL JR, 1991, ANN NY ACAD SCI, V627, P305
[3]   MOTONEURON PLASTICITY UNDERLYING OPERANTLY CONDITIONED DECREASE IN PRIMATE H-REFLEX [J].
CARP, JS ;
WOLPAW, JR .
JOURNAL OF NEUROPHYSIOLOGY, 1994, 72 (01) :431-442
[4]  
CONWAY BA, 1987, EXP BRAIN RES, V68, P643
[5]   LEARNING AND MEMORY IN THE VESTIBULOOCULAR REFLEX [J].
DULAC, S ;
RAYMOND, JL ;
SEJNOWSKI, TJ ;
LISBERGER, SG .
ANNUAL REVIEW OF NEUROSCIENCE, 1995, 18 :409-441
[6]   THE EFFECTS OF DISUSE AND OF ACTIVITY ON MAMMALIAN SPINAL REFLEXES [J].
ECCLES, JC ;
MCINTYRE, AK .
JOURNAL OF PHYSIOLOGY-LONDON, 1953, 121 (03) :492-516
[7]   DISUSE ENHANCES SYNAPTIC EFFICACY IN SPINAL MONONEURONES [J].
GALLEGO, R ;
KUNO, M ;
NUNEZ, R ;
SNIDER, WD .
JOURNAL OF PHYSIOLOGY-LONDON, 1979, 291 (JUN) :191-205
[8]   OCCURRENCE OF HETERONYMOUS MONOSYNAPTIC REFLEXES FOLLOWING TENOTOMY [J].
GOLDFARB, J ;
MULLER, RU .
BRAIN RESEARCH, 1971, 28 (03) :553-&
[9]  
GOSSARD JP, 1994, EXP BRAIN RES, V98, P213
[10]   ANKLE EXTENSOR GROUP-I AFFERENTS EXCITE EXTENSORS THROUGHOUT THE HINDLIMB DURING FICTIVE LOCOMOTION IN THE CAT [J].
GUERTIN, P ;
ANGEL, MJ ;
PERREAULT, MC ;
MCCREA, DA .
JOURNAL OF PHYSIOLOGY-LONDON, 1995, 487 (01) :197-209