ABSTRACT
Aberrant reinnervation of target organs caused by misdirected axonal growth at the
repair site is a major reason for the poor functional outcome usually seen after peripheral
nerve transection and repair. This study investigates whether the criss-crossing of
regenerating rat sciatic nerve axons between tibial and peroneal nerve fascicles can
be reduced by using non-vascularized autologous fascia as a barrier.
The left sciatic nerve was transected and repaired at midthigh as follows: epineurialy
sutures (Group A); fascicular repair of tibial and peroneal nerve fascicles (Group
B); fascicular repair of tibial and peroneal nerve fascicles separating the two fascicles
by non-vascularized autologous fascia (Group C). In the control Group D, only the
left tibial fascicle was transected and repaired. Five months postoperatively, the
outcome of regeneration was evaluated by histology, by retrograde tracing, and by
assessment of the contraction force of the gastrocnemius and tibial anterior muscles.
The tracing experiments showed that muscle reinnervation was less abnormal in Group
C than in Groups A and B. However, muscle contraction force was not better in Group
C than in Groups A and B. With respect to the peroneal nerve innervated muscle, the
contraction force in Group C was significantly lower than in Group B. The histologic
picture indicated that this inferior result in Group C was due to nerve compression
caused by fibrotic scar tissue at the site of the fascia graft.
Results of this study show that a non-vascularized autologous fascial graft used as
a barrier between two sutured nerve fascicles in adjacency reduces criss-crossing
of regenerating axons between the fascicles, but causes significant nerve compression.
KEYWORDS
Aberrant reinnervation - autologous fascia - sciatic nerve
REFERENCES
1
Fu S Y, Gordon T.
Contributing factors to poor functional recovery after delayed nerve repair: prolonged
axotomy.
J Neurosci.
1995;
15
3876-3885
2
Meyer R S, Abrams R A, Botte M J et al..
Functional recovery following neurorrhaphy of the rat sciatic nerve by epineurial
repair compared with tubulization.
J Orthop Res.
1997;
15
664-669
3
Rende M, Granato A, LoMonaco M, Zelano G, Toesca A.
Accuracy of reinnervation by peripheral nerve axons regenerating across a 10 mm gap
within a permeable chamber.
Exp Neurol.
1991;
111
332-339
4
Bodine-Fowler S C, Meyer S, Moskowitz A, Abrams R, Botte M J.
Inaccurate projection of rat soleus motoneurons: a comparison of nerve repair techniques.
Muscle Nerve.
1997;
20
29-37
5
Kline D G, Kim D, Midha R, Harsh C, Tiel R.
Management and results of sciatic nerve injuries: a 24-year experience.
J Neurosurg.
1998;
89
13-23
6
Monserrat L, Benito M.
Facial synkinesis and aberrant regeneration of the facial nerve.
Adv Neurol.
1988;
47
9-29
7
Sumner A J.
Aberrant reinnervation.
Muscle Nerve.
1990;
13
801-803
8 Cajal SR, May RM, trans; DeFelipe J, Jones EG Degeneration and Regeneration of the
Nervous System. New York; Oxford University Press Inc 1991
9 Sunderland S. Nerve Injuries and their Repair. A Critical Appraisal Edinburgh; Churchill
Livingstone 1991
10
Lundborg G, Dahlin L, Danielsen N, Zhao Q.
Trophism, tropism, and specificity in nerve regeneration.
J Reconstr Microsurg.
1994;
5
345-354
11
Cusick C G.
Extensive cortical reorganization following sciatic nerve injury in adult rats versus
restricted reorganization after neonatal injury: implications for spatial and temporal
limits on somatosensory plasticity.
Prog Brain Res.
1996;
108
379-390
12
Hendry I A, Hill C E, Watters D J.
Long-term retention of fast blue in sympathetic neurons after axotomy and regeneration-demonstration
of incorrect reconnections.
Brain. Res.
1986;
376
292-298
13
Aldskogius H, Molander C, Persson J, Thomander L.
Specific and non-specific regeneration of motor axons after sciatic nerve injury and
repair in the rat.
J Neurol Sci.
1087;
80
249-257
14
Zhao Q, Dahlin B, Kanje M, Lundborg G.
Specificity of muscle reinnervation following repair of the transected sciatic nerve.
J Hand Surg.
1992;
17B
257-261
15
Heumann R, Lindholm D, Bandtlow C et al..
Differential regulation of mRNA encoding nerve growth factor and its receptor in rat
sciatic nerves during development, degeneration and regeneration.
Proc Natl Acad Sci US.
1987;
84
8735-8739
16
Politis M J, Ederle K, Spencer P S.
Tropism in nerve regeneration in vivo. Attraction of regenerating axons by diffusable
factors derived from cells in distal nerve stumps of transected peripheral nerves.
Brain Res.
1982;
235
1-12
17
Raivich G, Kreuzberg G W.
Nerve growth factor and regeneration of peripheral nervous system.
Clin Neurol Neurosurg.
1993;
95
S103-S108
18
Weis J, Schroeder J M.
Differential effects of nerve, muscle, and fat tissue on regenerating nerve fibers
in vivo.
Muscle Nerve.
1989;
12
723-734
19
Brushart T M.
Preferential motor reinnervation: a sequential double-labeling study.
Restor Neurol Neurosci.
1990;
1
281-287
20
Brushart T M, Mathur V, Sood R, Koschorke G M.
Dispersion of regenerating axons across enclosed neural gaps.
J Hand Surg.
1995;
20A
557-564
21
Flanagan J G.
Life on the road.
Nature.
1999;
401
747-748
22
Mueller B K.
Growth cone guidance: first steps towards a deeper understanding.
Ann Rev Neurosci.
1999;
22
351-388
23
Ranscht B.
Cadherins: molecular codes for axon guidance and synapse formation.
Int J Dev Neurosci.
2000;
18
643-651
24
Lutz B S, Ma S F, Chuang D CC, Chan K H, Wei F C.
Interposition of a pedicle fat flap significantly improves specificity of reinnervation
and motor recovery after repair of transected nerves in adjacency in rats.
Plast Reconstr Surg.
2001;
107
116-123
25
Lutz B S, Ma S F, Chuang D CC, Lidman D, Wei F C.
Specificity of reinnervation and motor recovery after interposition of an artificial
barrier between transected and repaired nerves in adjacency-an experimental study
in the rat.
Acta Neurochir.
2001;
143
393-399
26
Disa J J, Klein M H, Goldberg N H.
Advantages of autologous fascia versus synthetic patch abdominal reconstruction in
experimental animal defects.
Plast Reconstr Surg.
1996;
97
801-806
27
Das S, Davidson S, Walker B et al..
The fate of free autogenous fascial grafts in the rabbit.
Br J Plast Surg.
1990;
43
315-317
28
Peimer C A, Heffner R R, Howard C S, Czyrny J J, Sherwin S S.
Peripheral nerve repair using non neural sheaths and conduits.
Hand Surg.
1996;
1
123-130
29
Mohammad J, Shenaq J, Rabinovsky E, Shenaq S.
Modulation of peripheral nerve regeneration: a tissue-engineering approach. The role
of amnion tube nerve conduit across a 1-centimeter nerve gap.
Plast Reconstr Surg.
2000;
105
660-666
30
Kuljis R O, De Carolis V, Fernandez V, Vincent O.
Observations on the early mechanisms of severed nerve regneration after compressive
tubulation repair.
Exp Neurol.
1983;
80
708-725
31
Lutz B S, Ma S F, Wei F C, Chuang D CC.
Effects of systemically applied IGF-1 on motor nerve recovery after peripheral nerve
transection and repair in the rat-a functional study.
Hand Surg.
1999;
4
131-136
32
Gramsbergen A, Ijkema-Paassen J, Meek M F.
Sciatic nerve transection in the adult rat: abnormal EMG patterns during locomotion
by aberrant innervation of hindleg muscles.
Exp Neurol.
2000;
161
183-193
33
Spector J G, Derby A, Lee P, Roufa D G.
Comparison of rabbit facial nerve regeneration in nerve growth factor-containing silicone
tubes to that in autologeous neural grafts.
Ann Otol Rhinol Laryngol.
1995;
104
875-885
34
Madorowski S J, Swett J E, Crumley R L.
Motor versus sensory neuron regeneration through collagen tubules.
Plast Reconstr Surg.
1998;
102
430-438
35 Peacock E E. Inflammation and the cellular response to injury. In: Peacock EE Wound
Repair. 3rd Philadelphia; W.B. Saunders 1984: 1-14
36
Rudolph R, Abraham J, Vecchione T et al..
Myofibroblasts and free silicon around breast implants.
Plast Reconstr Surg.
1987;
62
185-196
37
Chamberlain L J, Jannas I V, Hsu H P et al..
Connective tissue response to tubular implants for peripheral nerve regeneration:
the role of myofibroblasts.
J Comp Neurol.
2000;
417
415-430
38
Goldberg I, Knight K R, Mahoney J E et al..
A biochemical and histological comparison of vascularized and free fat grafts in the
rabbit.
Ann Plast Surg.
1993;
30
334-340
39
Sakamoto K.
Experimental study on pedicle fat grafts after laminectomy: comparison of pedicle
fat and free fat grafts [in Japanese].
Nippon Seikeigeka Gakkai Zasshi.
1987;
61
743-753
40
Lolley R D, Bose W J, Bastian F et al..
Vein, silastic, and polyglycolic acid fine mesh: a comparative study in peripheral
nerve repair.
Ann Plast Surg.
1995;
35
266-271
41
Heijke G C, Klopper P J, Dutrieux R P.
Vein graft conduits versus conventional suturing in peripheral nerve reconstructions.
Microsurgery.
1993;
14
584-588
Barbara S LutzM.D. Ph.D.
Department of Plastic Surgery, University Hospital Örebro
SE - 70185 Örebro, Sweden