Use of Erythropoietin as adjuvant therapy in nerve reconstruction.

Standard

Use of Erythropoietin as adjuvant therapy in nerve reconstruction. / Lohmeyer, J A; Essmann, E; Richerson, S J; Hagel, Christian; Egana, J T; Condurache, A; Ganske, P; Schulz, K; Mailänder, P; Machens, H G.

In: LANGENBECK ARCH SURG, Vol. 393, No. 3, 3, 2008, p. 317-323.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Lohmeyer, JA, Essmann, E, Richerson, SJ, Hagel, C, Egana, JT, Condurache, A, Ganske, P, Schulz, K, Mailänder, P & Machens, HG 2008, 'Use of Erythropoietin as adjuvant therapy in nerve reconstruction.', LANGENBECK ARCH SURG, vol. 393, no. 3, 3, pp. 317-323. <http://www.ncbi.nlm.nih.gov/pubmed/18299885?dopt=Citation>

APA

Lohmeyer, J. A., Essmann, E., Richerson, S. J., Hagel, C., Egana, J. T., Condurache, A., Ganske, P., Schulz, K., Mailänder, P., & Machens, H. G. (2008). Use of Erythropoietin as adjuvant therapy in nerve reconstruction. LANGENBECK ARCH SURG, 393(3), 317-323. [3]. http://www.ncbi.nlm.nih.gov/pubmed/18299885?dopt=Citation

Vancouver

Lohmeyer JA, Essmann E, Richerson SJ, Hagel C, Egana JT, Condurache A et al. Use of Erythropoietin as adjuvant therapy in nerve reconstruction. LANGENBECK ARCH SURG. 2008;393(3):317-323. 3.

Bibtex

@article{0e59d5989e1845069a16caf1b1512a2f,
title = "Use of Erythropoietin as adjuvant therapy in nerve reconstruction.",
abstract = "BACKGROUND AND AIMS: Adjuvant therapies may improve the outcome after nerve reconstruction. We analyzed the influence of recombinant human Erythropoietin (rHuEpo), which has proven angiogenic and neuroprotective effects, on the quality of peripheral nerve regeneration. METHODS: Thirty two female Lewis rats underwent nerve reconstruction by means of tubulization (groups I and II) or autologous sciatic nerve grafting (groups III and IV). Groups I and III received daily subcutaneous rHuEpo injections over 2 weeks (1,000 U/kg bw) with normal saline injections as controls (groups II and IV). Data on histology and muscle weight were collected after 7 weeks. Axon count and diameter were assessed by a new method based on digital segmentation. RESULTS: Atrophy of the tibial muscle was less severe in the rHuEpo-treated group compared to controls resulting in significant higher muscle weight quotients (p = 0.006). The same trend was found in the gastrocnemius muscle, but without being statistically significant. No significant differences in axon count or axon diameter were detected in the presence of rHuEpo treatments. CONCLUSION: Our findings give evidence for a positive effect of Erythropoietin on functional recovery after nerve grafting. Muscle recovery benefited from rHuEpo administration despite absence of improved neural morphology. Semi-automated axon detection facilitated accurate morphometrical assessment.",
author = "Lohmeyer, {J A} and E Essmann and Richerson, {S J} and Christian Hagel and Egana, {J T} and A Condurache and P Ganske and K Schulz and P Mail{\"a}nder and Machens, {H G}",
year = "2008",
language = "Deutsch",
volume = "393",
pages = "317--323",
journal = "LANGENBECK ARCH SURG",
issn = "1435-2443",
publisher = "Springer",
number = "3",

}

RIS

TY - JOUR

T1 - Use of Erythropoietin as adjuvant therapy in nerve reconstruction.

AU - Lohmeyer, J A

AU - Essmann, E

AU - Richerson, S J

AU - Hagel, Christian

AU - Egana, J T

AU - Condurache, A

AU - Ganske, P

AU - Schulz, K

AU - Mailänder, P

AU - Machens, H G

PY - 2008

Y1 - 2008

N2 - BACKGROUND AND AIMS: Adjuvant therapies may improve the outcome after nerve reconstruction. We analyzed the influence of recombinant human Erythropoietin (rHuEpo), which has proven angiogenic and neuroprotective effects, on the quality of peripheral nerve regeneration. METHODS: Thirty two female Lewis rats underwent nerve reconstruction by means of tubulization (groups I and II) or autologous sciatic nerve grafting (groups III and IV). Groups I and III received daily subcutaneous rHuEpo injections over 2 weeks (1,000 U/kg bw) with normal saline injections as controls (groups II and IV). Data on histology and muscle weight were collected after 7 weeks. Axon count and diameter were assessed by a new method based on digital segmentation. RESULTS: Atrophy of the tibial muscle was less severe in the rHuEpo-treated group compared to controls resulting in significant higher muscle weight quotients (p = 0.006). The same trend was found in the gastrocnemius muscle, but without being statistically significant. No significant differences in axon count or axon diameter were detected in the presence of rHuEpo treatments. CONCLUSION: Our findings give evidence for a positive effect of Erythropoietin on functional recovery after nerve grafting. Muscle recovery benefited from rHuEpo administration despite absence of improved neural morphology. Semi-automated axon detection facilitated accurate morphometrical assessment.

AB - BACKGROUND AND AIMS: Adjuvant therapies may improve the outcome after nerve reconstruction. We analyzed the influence of recombinant human Erythropoietin (rHuEpo), which has proven angiogenic and neuroprotective effects, on the quality of peripheral nerve regeneration. METHODS: Thirty two female Lewis rats underwent nerve reconstruction by means of tubulization (groups I and II) or autologous sciatic nerve grafting (groups III and IV). Groups I and III received daily subcutaneous rHuEpo injections over 2 weeks (1,000 U/kg bw) with normal saline injections as controls (groups II and IV). Data on histology and muscle weight were collected after 7 weeks. Axon count and diameter were assessed by a new method based on digital segmentation. RESULTS: Atrophy of the tibial muscle was less severe in the rHuEpo-treated group compared to controls resulting in significant higher muscle weight quotients (p = 0.006). The same trend was found in the gastrocnemius muscle, but without being statistically significant. No significant differences in axon count or axon diameter were detected in the presence of rHuEpo treatments. CONCLUSION: Our findings give evidence for a positive effect of Erythropoietin on functional recovery after nerve grafting. Muscle recovery benefited from rHuEpo administration despite absence of improved neural morphology. Semi-automated axon detection facilitated accurate morphometrical assessment.

M3 - SCORING: Zeitschriftenaufsatz

VL - 393

SP - 317

EP - 323

JO - LANGENBECK ARCH SURG

JF - LANGENBECK ARCH SURG

SN - 1435-2443

IS - 3

M1 - 3

ER -