Negative Pressure Neurogenesis: A Novel Approach to Accelerate Nerve Regeneration after Complete Peripheral Nerve Transection
Background:. Various modalities to facilitate nerve regeneration have been described in the literature with limited success. We hypothesized that negative pressure applied to a sectioned peripheral nerve would enhance nerve regeneration by promoting angiogenesis and axonal lengthening. Methods:. Wis...
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Wolters Kluwer
2021-05-01
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doaj-ee64a494a2af4431a1ef988c0d300d902021-05-25T02:16:50ZengWolters KluwerPlastic and Reconstructive Surgery, Global Open2169-75742021-05-0195e356810.1097/GOX.0000000000003568202105000-00015Negative Pressure Neurogenesis: A Novel Approach to Accelerate Nerve Regeneration after Complete Peripheral Nerve TransectionTamer Mettyas, MBBCh, MSc, MRCS, FRACS0Matthew Barton, BMedSci, PhD1Muhammad Sana Ullah Sahar, MS2Felicity Lawrence, MAppSc3Alvaro Sanchez-Herrero, PharmD, MSc4Megha Shah, MBBS, MD5James St John, PhD6Randy Bindra, MBBS, FRACS, FRCS, MS, MCh, FAOrthA7From the * Department of Orthopaedics, Queen Elizabeth II Hospital, Brisbane, Queensland, Australia† School of Nursing and Midwifery, Griffith University, Australia¶ School of Engineering and Built Environment, Griffith University, Australia** Institute of Health and Biomedical Innovation, Queensland University of Technology, Australia†† Centre for Regenerative Medicine, Queensland University of Technology, Australia‡ Menzies Health Institute Queensland, Griffith University, Australia‡ Menzies Health Institute Queensland, Griffith University, Australia§§ School of Medicine, Griffith University, AustraliaBackground:. Various modalities to facilitate nerve regeneration have been described in the literature with limited success. We hypothesized that negative pressure applied to a sectioned peripheral nerve would enhance nerve regeneration by promoting angiogenesis and axonal lengthening. Methods:. Wistar rats’ sciatic nerves were cut (creating ~7 mm nerve gap) and placed into a silicone T-tube, to which negative pressure was applied. The rats were divided into 4 groups: control (no pressure), group A (low pressure: 10 mm Hg), group B (medium pressure: 20/30 mm Hg) and group C (high pressure: 50/70 mm Hg). The nerve segments were retrieved after 7 days for gross and histological analysis. Results:. In total, 22 rats completed the study. The control group showed insignificant nerve growth, whereas the 3 negative pressure groups showed nerve growth and nerve gap reduction. The true nerve growth was highest in group A (median: 3.54 mm) compared to group B, C, and control (medians: 1.19 mm, 1.3 mm, and 0.35 mm); however, only group A was found to be significantly different to the control group (**P < 0.01). Similarly, angiogenesis was observed to be significantly greater in group A (**P < 0.01) in comparison to the control. Conclusions:. Negative pressure stimulated nerve lengthening and angiogenesis within an in vivo rat model. Low negative pressure (10 mm Hg) provided superior results over the higher negative pressure groups and the control, favoring axonal growth. Further studies are required with greater number of rats and longer recovery time to assess the functional outcome.http://journals.lww.com/prsgo/fulltext/10.1097/GOX.0000000000003568 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tamer Mettyas, MBBCh, MSc, MRCS, FRACS Matthew Barton, BMedSci, PhD Muhammad Sana Ullah Sahar, MS Felicity Lawrence, MAppSc Alvaro Sanchez-Herrero, PharmD, MSc Megha Shah, MBBS, MD James St John, PhD Randy Bindra, MBBS, FRACS, FRCS, MS, MCh, FAOrthA |
spellingShingle |
Tamer Mettyas, MBBCh, MSc, MRCS, FRACS Matthew Barton, BMedSci, PhD Muhammad Sana Ullah Sahar, MS Felicity Lawrence, MAppSc Alvaro Sanchez-Herrero, PharmD, MSc Megha Shah, MBBS, MD James St John, PhD Randy Bindra, MBBS, FRACS, FRCS, MS, MCh, FAOrthA Negative Pressure Neurogenesis: A Novel Approach to Accelerate Nerve Regeneration after Complete Peripheral Nerve Transection Plastic and Reconstructive Surgery, Global Open |
author_facet |
Tamer Mettyas, MBBCh, MSc, MRCS, FRACS Matthew Barton, BMedSci, PhD Muhammad Sana Ullah Sahar, MS Felicity Lawrence, MAppSc Alvaro Sanchez-Herrero, PharmD, MSc Megha Shah, MBBS, MD James St John, PhD Randy Bindra, MBBS, FRACS, FRCS, MS, MCh, FAOrthA |
author_sort |
Tamer Mettyas, MBBCh, MSc, MRCS, FRACS |
title |
Negative Pressure Neurogenesis: A Novel Approach to Accelerate Nerve Regeneration after Complete Peripheral Nerve Transection |
title_short |
Negative Pressure Neurogenesis: A Novel Approach to Accelerate Nerve Regeneration after Complete Peripheral Nerve Transection |
title_full |
Negative Pressure Neurogenesis: A Novel Approach to Accelerate Nerve Regeneration after Complete Peripheral Nerve Transection |
title_fullStr |
Negative Pressure Neurogenesis: A Novel Approach to Accelerate Nerve Regeneration after Complete Peripheral Nerve Transection |
title_full_unstemmed |
Negative Pressure Neurogenesis: A Novel Approach to Accelerate Nerve Regeneration after Complete Peripheral Nerve Transection |
title_sort |
negative pressure neurogenesis: a novel approach to accelerate nerve regeneration after complete peripheral nerve transection |
publisher |
Wolters Kluwer |
series |
Plastic and Reconstructive Surgery, Global Open |
issn |
2169-7574 |
publishDate |
2021-05-01 |
description |
Background:. Various modalities to facilitate nerve regeneration have been described in the literature with limited success. We hypothesized that negative pressure applied to a sectioned peripheral nerve would enhance nerve regeneration by promoting angiogenesis and axonal lengthening.
Methods:. Wistar rats’ sciatic nerves were cut (creating ~7 mm nerve gap) and placed into a silicone T-tube, to which negative pressure was applied. The rats were divided into 4 groups: control (no pressure), group A (low pressure: 10 mm Hg), group B (medium pressure: 20/30 mm Hg) and group C (high pressure: 50/70 mm Hg). The nerve segments were retrieved after 7 days for gross and histological analysis.
Results:. In total, 22 rats completed the study. The control group showed insignificant nerve growth, whereas the 3 negative pressure groups showed nerve growth and nerve gap reduction. The true nerve growth was highest in group A (median: 3.54 mm) compared to group B, C, and control (medians: 1.19 mm, 1.3 mm, and 0.35 mm); however, only group A was found to be significantly different to the control group (**P < 0.01). Similarly, angiogenesis was observed to be significantly greater in group A (**P < 0.01) in comparison to the control.
Conclusions:. Negative pressure stimulated nerve lengthening and angiogenesis within an in vivo rat model. Low negative pressure (10 mm Hg) provided superior results over the higher negative pressure groups and the control, favoring axonal growth. Further studies are required with greater number of rats and longer recovery time to assess the functional outcome. |
url |
http://journals.lww.com/prsgo/fulltext/10.1097/GOX.0000000000003568 |
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