Characterization of spindle afferents in rat soleus muscle using ramp-and-hold and sinusoidal stretches

被引:37
作者
De-Doncker, L
Picquet, F
Petit, J
Falempin, M
机构
[1] Univ Sci & Technol Lille 1, IFR 118, EA 1032, Lab Plast Neuromusculaire, F-59655 Villeneuve Dascq, France
[2] Univ Bordeaux 2, Fac Sci Sport & Educ Phys, F-33607 Pessac, France
关键词
D O I
10.1152/jn.00153.2002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The discharge properties of 51 afferents were studied in the rat soleus muscle spindles. Under deep anesthesia using a pentobarbital sodium solution (30 mg/kg), a laminectomy was performed and the right L-4 and L-5 dorsal and ventral roots were transected near their entry into the spinal cord. In situ, the minimal (L-min) muscle length [3 +/- 0.08 (SE) cm] of the soleus was measured at full ankle extension. Unitary potentials from the L-5 dorsal root were recorded in response to ramp-and-hold stretches applied at 3 mm (S3) and 4 mm (S4) amplitudes and four stretch velocities (6, 10, 15, and 30 mm/s), sinusoidal stretches performed at four amplitudes (0.12, 0.25, 0.5, and 1 mm) and six stretch frequencies (0.5, 1, 2, 3, 6, and 10 Hz), and vibrations applied at 50-, 100-, and 150- Hz frequencies. These two kinds of stretches were performed at three different muscle lengths (Lmin+10%, Lmin+15%, and Lmin+20%), whereas vibrations were applied at Lmin+20% muscle length. Conduction velocity of the fibers was calculated but did not allow to discriminate different fiber types. However, the mean conduction velocity of the first fiber group (43.3 +/- 0.8 m/s) was significantly higher than that of the second fiber group (33.9 +/- 0.9 m/s). Three parameters allowed to differentiate the responses of primary and secondary endings: the dynamic index (DI), the discharge during the stretch release from the ramp-and-hold stretches, and the linear range and the vibration sensitivity from sinusoidal stretches. The slope histogram of the linear regression based on the DI and the stretch velocity was clearly bimodal. Therefore the responses were separated into two groups. During the stretch release at a velocity of 3 mm/s, the first response group (n = 26) exhibited a pause, whereas the second (n = 25) did not. The linear range of the second ending group (0.12-1 mm) was broader than that of the first (0.12-0.25 mm). The first ending group showed a higher sensitivity to high-vibration frequencies of small amplitude than the second. In comparison with the literature, we can assert that the first and the second ending groups corresponded to the primary and secondary endings, respectively. In conclusion, our study showed that in rat soleus muscle spindles, it was possible to immediately classify the discharge of Ia and II fibers by using some parameters measured under ramp-and-hold and sinusoidal stretches.
引用
收藏
页码:442 / 449
页数:8
相关论文
共 48 条
[1]   DISTRIBUTION AND PROPERTIES OF MUSCLE-SPINDLES IN CAUDAL SEGMENTAL MUSCLES OF RAT TOGETHER WITH SOME COMPARISONS WITH HIND LIMB MUSCLE-SPINDLES [J].
ANDREW, BL ;
LESLIE, GC ;
THOMPSON, J .
QUARTERLY JOURNAL OF EXPERIMENTAL PHYSIOLOGY AND COGNATE MEDICAL SCIENCES, 1973, 58 (01) :19-37
[2]  
ARBUTHNOTT ER, 1989, J ANAT, V163, P183
[3]   FORM AND DISTRIBUTION OF SENSORY TERMINALS IN CAT HINDLIMB MUSCLE-SPINDLES [J].
BANKS, RW ;
BARKER, D ;
STACEY, MJ .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1982, 299 (1096) :329-&
[4]   THE MOTOR INNERVATION OF MAMMALIAN MUSCLE-SPINDLES [J].
BANKS, RW .
PROGRESS IN NEUROBIOLOGY, 1994, 43 (4-5) :323-&
[5]  
Boyd I.A., 1981, MUSCLE RECEPTORS MOV, P17
[6]  
Boyd I.A., 1968, COMPOSITION PERIPHER
[7]   CONTROL OF DYNAMIC AND STATIC NUCLEAR BAG FIBERS AND NUCLEAR CHAIN FIBERS BY GAMMA-AXONS AND BETA-AXONS IN ISOLATED CAT MUSCLE-SPINDLES [J].
BOYD, IA ;
GLADDEN, MH ;
MCWILLIAM, PN ;
WARD, J .
JOURNAL OF PHYSIOLOGY-LONDON, 1977, 265 (01) :133-&
[9]   RELATIVE SENSITIVITY TO VIBRATION OF MUSCLE RECEPTORS OF CAT [J].
BROWN, MC ;
ENGBERG, I ;
MATTHEWS, PB .
JOURNAL OF PHYSIOLOGY-LONDON, 1967, 192 (03) :773-&
[10]  
CHENEY PD, 1976, J NEUROPHYSIOL, V39, P1