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Transforming Growth Factor-β-Activated Kinase 1 (TAK1) Mediates Chronic Pain and Cytokine Production in Mouse Models of Inflammatory, Neuropathic, and Primary Pain.

Publication ,  Journal Article
Scarneo, S; Zhang, X; Wang, Y; Camacho-Domenech, J; Ricano, J; Hughes, P; Haystead, T; Nackley, AG
Published in: J Pain
September 2023

The origin of chronic pain is linked to inflammation, characterized by increased levels of proinflammatory cytokines in local tissues and systemic circulation. Transforming growth factor beta-activated kinase 1 (TAK1) is a key regulator of proinflammatory cytokine signaling that has been well characterized in the context of cancer and autoimmune disorders, yet its role in chronic pain is less clear. Here, we evaluated the ability of our TAK1 small-molecule inhibitor, takinib, to attenuate pain and inflammation in preclinical models of inflammatory, neuropathic, and primary pain. Inflammatory, neuropathic, and primary pain was modeled using intraplantar complete Freund's adjuvant (CFA), chronic constriction injury (CCI), and systemic delivery of the catechol-O-methyltransferase (COMT) inhibitor OR486, respectively. Behavioral responses evoked by mechanical and thermal stimuli were evaluated in separate groups of mice receiving takinib or vehicle prior to pain induction (baseline) and over 12 days following CFA injection, 4 weeks following CCI surgery, and 6 hours following OR486 delivery. Hindpaw edema was also measured prior to and 3 days following CFA injection. Upon termination of behavioral experiments, dorsal root ganglia (DRG) were collected to measure cytokines. We also evaluated the ability of takinib to modulate nociceptor activity via in vitro calcium imaging of neurons isolated from the DRG of Gcamp3 mice. In all 3 models, TAK1 inhibition significantly reduced hypersensitivity to mechanical and thermal stimuli and expression of proinflammatory cytokines in DRG. Furthermore, TAK1 inhibition significantly reduced the activity of tumor necrosis factor (TNF)-primed/capsaicin-evoked DRG nociceptive neurons. Overall, our results support the therapeutic potential of TAK1 as a novel drug target for the treatment of chronic pain syndromes with different etiologies. PERSPECTIVE: This article reports the therapeutic potential of TAK1 inhibitors for the treatment of chronic pain. This new treatment has the potential to provide a greater therapeutic offering to physicians and patients suffering from chronic pain as well as reduce the dependency on opioid-based pain treatments.

Duke Scholars

Published In

J Pain

DOI

EISSN

1528-8447

Publication Date

September 2023

Volume

24

Issue

9

Start / End Page

1633 / 1644

Location

United States

Related Subject Headings

  • Rats, Sprague-Dawley
  • Rats
  • Mice
  • Inflammation
  • Hyperalgesia
  • Ganglia, Spinal
  • Freund's Adjuvant
  • Disease Models, Animal
  • Cytokines
  • Chronic Pain
 

Citation

APA
Chicago
ICMJE
MLA
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Scarneo, S., Zhang, X., Wang, Y., Camacho-Domenech, J., Ricano, J., Hughes, P., … Nackley, A. G. (2023). Transforming Growth Factor-β-Activated Kinase 1 (TAK1) Mediates Chronic Pain and Cytokine Production in Mouse Models of Inflammatory, Neuropathic, and Primary Pain. J Pain, 24(9), 1633–1644. https://doi.org/10.1016/j.jpain.2023.04.011
Scarneo, Scott, Xin Zhang, Yaomin Wang, Jose Camacho-Domenech, Jennifer Ricano, Philip Hughes, Tim Haystead, and Andrea G. Nackley. “Transforming Growth Factor-β-Activated Kinase 1 (TAK1) Mediates Chronic Pain and Cytokine Production in Mouse Models of Inflammatory, Neuropathic, and Primary Pain.J Pain 24, no. 9 (September 2023): 1633–44. https://doi.org/10.1016/j.jpain.2023.04.011.
Scarneo, Scott, et al. “Transforming Growth Factor-β-Activated Kinase 1 (TAK1) Mediates Chronic Pain and Cytokine Production in Mouse Models of Inflammatory, Neuropathic, and Primary Pain.J Pain, vol. 24, no. 9, Sept. 2023, pp. 1633–44. Pubmed, doi:10.1016/j.jpain.2023.04.011.
Scarneo S, Zhang X, Wang Y, Camacho-Domenech J, Ricano J, Hughes P, Haystead T, Nackley AG. Transforming Growth Factor-β-Activated Kinase 1 (TAK1) Mediates Chronic Pain and Cytokine Production in Mouse Models of Inflammatory, Neuropathic, and Primary Pain. J Pain. 2023 Sep;24(9):1633–1644.
Journal cover image

Published In

J Pain

DOI

EISSN

1528-8447

Publication Date

September 2023

Volume

24

Issue

9

Start / End Page

1633 / 1644

Location

United States

Related Subject Headings

  • Rats, Sprague-Dawley
  • Rats
  • Mice
  • Inflammation
  • Hyperalgesia
  • Ganglia, Spinal
  • Freund's Adjuvant
  • Disease Models, Animal
  • Cytokines
  • Chronic Pain