Dorsal root ganglia grafts stimulate regeneration of denervated urodele forelimbs: timing of graft implantation with respect to denervation

Development ◽  
1987 ◽  
Vol 99 (2) ◽  
pp. 173-186
Author(s):  
B.L. Tomlinson ◽  
R.A. Tassava

Amphibian forelimb regeneration is a nerve-dependent process; nerves presumably release one or more neurotrophic factors that stimulate blastema cell division. To date several candidate molecules/factors have been shown to stimulate macromolecular synthesis and/or mitosis but sustained cell cycle activity and blastema development have not been achieved. Because dorsal root ganglia (DRG) implants are capable of promoting regeneration of denervated adult newt limbs (Kamrin & Singer, 1959), we have evaluated the DRG stimulation of regeneration in denervated limbs of adult newts and larval axolotls; two alternative timing strategies were tested as a step toward defining bioassay parameters that best reflect neurotrophic activity. The frequency of regeneration in denervated adult newt limbs was compared after providing DRG before or at the time of denervation (to maintain neurotrophic and cell cycle activity) versus DRG implantation at various postdenervation times (to resupply neurotrophic activity and restimulate suppressed cell cycle activity). The results show that denervated adult newt limbs regenerated most frequently using the maintenance strategy, but as the denervation interval was extended in the restimulation strategy, the frequency of regeneration declined. Larval axolotl limbs responded positively in both maintenance and restimulation DRG-grafting protocols. These results suggest that the efficacy of DRG stimulation of regeneration in adult newts was related to the relative number of blastema cells present at the time of denervation and the proliferative status of the blastema cells; bioassays with denervated adult newt limbs should be designed with these constraints in mind. Because such constraints are not as problematic with the larval axolotl, this species may provide the best opportunity for further defining bioassay parameters related to the neurotrophic stimulation of regeneration.

Pain Practice ◽  
2014 ◽  
Vol 15 (3) ◽  
pp. 208-216 ◽  
Author(s):  
Jean-Pierre Van Buyten ◽  
Iris Smet ◽  
Liong Liem ◽  
Marc Russo ◽  
Frank Huygen

Spine ◽  
1987 ◽  
Vol 12 (6) ◽  
pp. 552-555 ◽  
Author(s):  
MARIE A. BADALAMENTE ◽  
ROGER DEE ◽  
RICHARD GHILLANI ◽  
PU-FAN CHIEN ◽  
KENNEDY DANIELS

Pain Practice ◽  
2017 ◽  
Vol 18 (2) ◽  
pp. 205-213 ◽  
Author(s):  
Frank Huygen ◽  
Liong Liem ◽  
William Cusack ◽  
Jeffery Kramer

2004 ◽  
Vol 361 (1-3) ◽  
pp. 32-35 ◽  
Author(s):  
S. Papadopolou ◽  
P. Hartmann ◽  
K.S. Lips ◽  
W. Kummer ◽  
R.V. Haberberger

Spine ◽  
1990 ◽  
Vol 15 (12) ◽  
pp. 1252-1256 ◽  
Author(s):  
A. PEDRINI-MILLE ◽  
J. N. WEINSTEIN ◽  
E. M. FOUND ◽  
C. B. CHUNG ◽  
V. K. GOEL

1993 ◽  
Vol 70 (6) ◽  
pp. 2350-2353 ◽  
Author(s):  
Z. Wiesenfeld-Hallin ◽  
J. X. Hao ◽  
X. J. Xu ◽  
T. Hokfelt

1. We have examined the effect of intravenously injected nitro-L-arginine methyl ester (L-NAME), inhibitor of nitric oxide (NO) synthase, on the ongoing discharges originating in dorsal root ganglia in rats. 2. Ongoing activity was recorded from dorsal rootlets that were responsive to electrical stimulation of the axotomized sciatic nerve. Resection of the nerve proximal to the neuroma did not appreciably influence the rate of ongoing activity. Intravenous L-NAME (100 and 200 mumol/kg) suppressed ongoing activity both when the neuroma was intact or acutely resected. The effect of L-NAME was reversed by L-arginine (575 and 1,150 mumol/kg). 3. L-NAME had no effect on ongoing activity recorded from dorsal rootlets in normal rats or rootlets with no sciatic input in axotomized rats. 4. No ongoing activity could be recorded from sciatic nerve filaments that had been sectioned proximally before the recording in axotomized rats, although a response could be elicited by mechanical stimulation of the neuroma. 5. Because peripheral axotomy has been shown to markedly increase the level of mRNA for NO synthase in dorsal root ganglion cells, the present results indicate that NO may be involved in the generation of spontaneous discharges in deafferentated dorsal root ganglia.


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