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Targeting anti-inflammatory treatment can ameliorate injury-induced neuropathic pain.

Iwatsuki K, Arai T, Ota H, Kato S, Natsume T, Kurimoto S, Yamamoto M, Hirata H - PLoS ONE (2013)

Bottom Line: Etanercept treatment improved recovery of motor nerve conduction velocity, muscle weight loss, and sciatic functional index.Etanercept reduced expression of interleukin-6 and monocyte chemotactic and activating factor-1 at the crushed sciatic nerve.Etanercept does not impede the onset or progression of Wallerian degeneration, but optimizes the involvement of macrophages and the secretion of inflammatory mediators.

View Article: PubMed Central - PubMed

Affiliation: Department of Hand Surgery, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, Japan. kiwatsuki@med.nagoya-u.ac.jp

ABSTRACT
Tumor necrosis factor-α plays important roles in immune system development, immune response regulation, and T-cell-mediated tissue injury. The present study assessed the net value of anti-tumor necrosis factor-α treatment in terms of functional recovery and inhibition of hypersensitivity after peripheral nerve crush injury. We created a right sciatic nerve crush injury model using a Sugita aneurysm clip. Animals were separated into 3 groups: the first group received only a skin incision; the second group received nerve crush injury and intraperitoneal vehicle injection; and the third group received nerve crush injury and intraperitoneal etanercept (6 mg/kg). Etanercept treatment improved recovery of motor nerve conduction velocity, muscle weight loss, and sciatic functional index. Plantar thermal and von Frey mechanical withdrawal thresholds recovered faster in the etanercept group than in the control group. On day 7 after crush injury, the numbers of ED-1-positive cells in crushed nerves of the control and etanercept groups were increased compared to that in the sham-treated group. After 21 days, ED-1-positive cells had nearly disappeared from the etanercept group. Etanercept reduced expression of interleukin-6 and monocyte chemotactic and activating factor-1 at the crushed sciatic nerve. These findings demonstrate the utility of etanercept, in terms of both enhancing functional recovery and suppressing hypersensitivity after nerve crush. Etanercept does not impede the onset or progression of Wallerian degeneration, but optimizes the involvement of macrophages and the secretion of inflammatory mediators.

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Related in: MedlinePlus

Effect of etanercept on wet muscle weight measurement.Control group showed a significantly lower percentage of wet muscle weight than the etanercept group on day 21 (**p<0.01).
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pone-0057721-g002: Effect of etanercept on wet muscle weight measurement.Control group showed a significantly lower percentage of wet muscle weight than the etanercept group on day 21 (**p<0.01).

Mentions: The etanercept and control groups exhibited significantly lower percentage wet muscle weights than the sham group on days 21 and 35 (Fig. 2). Furthermore, the control group exhibited a significantly lower percentage wet muscle weight than the etanercept group on day 21. However, on day 35, no significant difference was observed between the etanercept and control groups.


Targeting anti-inflammatory treatment can ameliorate injury-induced neuropathic pain.

Iwatsuki K, Arai T, Ota H, Kato S, Natsume T, Kurimoto S, Yamamoto M, Hirata H - PLoS ONE (2013)

Effect of etanercept on wet muscle weight measurement.Control group showed a significantly lower percentage of wet muscle weight than the etanercept group on day 21 (**p<0.01).
© Copyright Policy
Related In: Results  -  Collection

Show All Figures
getmorefigures.php?uid=PMC3585184&req=5

pone-0057721-g002: Effect of etanercept on wet muscle weight measurement.Control group showed a significantly lower percentage of wet muscle weight than the etanercept group on day 21 (**p<0.01).
Mentions: The etanercept and control groups exhibited significantly lower percentage wet muscle weights than the sham group on days 21 and 35 (Fig. 2). Furthermore, the control group exhibited a significantly lower percentage wet muscle weight than the etanercept group on day 21. However, on day 35, no significant difference was observed between the etanercept and control groups.

Bottom Line: Etanercept treatment improved recovery of motor nerve conduction velocity, muscle weight loss, and sciatic functional index.Etanercept reduced expression of interleukin-6 and monocyte chemotactic and activating factor-1 at the crushed sciatic nerve.Etanercept does not impede the onset or progression of Wallerian degeneration, but optimizes the involvement of macrophages and the secretion of inflammatory mediators.

View Article: PubMed Central - PubMed

Affiliation: Department of Hand Surgery, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, Japan. kiwatsuki@med.nagoya-u.ac.jp

ABSTRACT
Tumor necrosis factor-α plays important roles in immune system development, immune response regulation, and T-cell-mediated tissue injury. The present study assessed the net value of anti-tumor necrosis factor-α treatment in terms of functional recovery and inhibition of hypersensitivity after peripheral nerve crush injury. We created a right sciatic nerve crush injury model using a Sugita aneurysm clip. Animals were separated into 3 groups: the first group received only a skin incision; the second group received nerve crush injury and intraperitoneal vehicle injection; and the third group received nerve crush injury and intraperitoneal etanercept (6 mg/kg). Etanercept treatment improved recovery of motor nerve conduction velocity, muscle weight loss, and sciatic functional index. Plantar thermal and von Frey mechanical withdrawal thresholds recovered faster in the etanercept group than in the control group. On day 7 after crush injury, the numbers of ED-1-positive cells in crushed nerves of the control and etanercept groups were increased compared to that in the sham-treated group. After 21 days, ED-1-positive cells had nearly disappeared from the etanercept group. Etanercept reduced expression of interleukin-6 and monocyte chemotactic and activating factor-1 at the crushed sciatic nerve. These findings demonstrate the utility of etanercept, in terms of both enhancing functional recovery and suppressing hypersensitivity after nerve crush. Etanercept does not impede the onset or progression of Wallerian degeneration, but optimizes the involvement of macrophages and the secretion of inflammatory mediators.

Show MeSH
Related in: MedlinePlus