Differential impact of psychological and psychophysical stress on low back pain in mice
- PMID: 32132393
- DOI: 10.1097/j.pain.0000000000001850
Differential impact of psychological and psychophysical stress on low back pain in mice
Abstract
Low back pain (LBP) is a highly prevalent and disabling condition whose initiating factors are poorly understood. It is known that psychological and physical stress is associated with LBP but the causal relationship, mechanisms, and mediators have not been elucidated, and a preclinical model enabling the investigation of causality and thereby critically contributing to clinical translation does not exist. In this study, we first established and characterized a myofascial LBP model in mice based on nerve growth factor (NGF) injection into the low back muscles. Second, we investigated the effect of 2 different stress paradigms on this mouse LBP model by applying the chronic unpredictable stress and vertical chronic restraint stress (vCRS) paradigms, to mimic psychological and psychophysical stress, respectively. In these studies, we combined longitudinal behavioral tests with gene and protein expression analysis in the muscle, dorsal root ganglia, and spinal cord. Nerve growth factor-induced LBP was characterized by long-lasting local and plantar mechanical hypersensitivity, cold hyperalgesia, decreased grip strength and wheel running activity, and time-dependent changes of neuropeptide and glial markers in the spinal cord. Interestingly, the exposure to chronic unpredictable stress slightly worsened pain behavior, whereas vCRS primed and highly aggravated pain in this LBP model, by causing per se the intramuscular upregulation of endogenous NGF and increased spinal astrocyte expression. Our mouse model, particularly the combination of NGF injection and vCRS, suggests that similar mechanisms are important in nonspecific LBP and might help to investigate certain aspects of stress-induced exacerbation of pain.
Similar articles
-
ISSLS Prize winner: Increased innervation and sensory nervous system plasticity in a mouse model of low back pain due to intervertebral disc degeneration.Spine (Phila Pa 1976). 2014 Aug 1;39(17):1345-54. doi: 10.1097/BRS.0000000000000334. Spine (Phila Pa 1976). 2014. PMID: 24718079
-
Somatosensory behavioral alterations in a NGF-induced persistent low back pain model.Behav Brain Res. 2022 Feb 10;418:113617. doi: 10.1016/j.bbr.2021.113617. Epub 2021 Oct 2. Behav Brain Res. 2022. PMID: 34606776
-
Animal models for studying the etiology and treatment of low back pain.J Orthop Res. 2018 May;36(5):1305-1312. doi: 10.1002/jor.23741. Epub 2018 Mar 14. J Orthop Res. 2018. PMID: 28921656 Free PMC article. Review.
-
The Different Dynamic Changes of Nerve Growth Factor in the Dorsal Horn and Dorsal Root Ganglion Leads to Hyperalgesia and Allodynia in Diabetic Neuropathic Pain.Pain Physician. 2017 May;20(4):E551-E561. Pain Physician. 2017. PMID: 28535564
-
Diagnostic evaluation of low back pain.Orthop Clin North Am. 2004 Jan;35(1):7-16. doi: 10.1016/S0030-5898(03)00099-3. Orthop Clin North Am. 2004. PMID: 15062713 Review.
Cited by
-
Chronic musculoskeletal pain: traps and pitfalls in classification and management of a major global disease burden.Pain Rep. 2022 Aug 9;7(5):e1023. doi: 10.1097/PR9.0000000000001023. eCollection 2022 Sep-Oct. Pain Rep. 2022. PMID: 35975138 Free PMC article.
-
Persistent pain signaling and stress response in a mouse model of inflammatory low back pain.Pain Rep. 2025 Jun 25;10(4):e1300. doi: 10.1097/PR9.0000000000001300. eCollection 2025 Aug. Pain Rep. 2025. PMID: 40575733 Free PMC article.
-
Evidence of a new hidden neural network into deep fasciae.Sci Rep. 2021 Jun 16;11(1):12623. doi: 10.1038/s41598-021-92194-z. Sci Rep. 2021. PMID: 34135423 Free PMC article.
-
Acute inflammatory response via neutrophil activation protects against the development of chronic pain.Sci Transl Med. 2022 May 11;14(644):eabj9954. doi: 10.1126/scitranslmed.abj9954. Epub 2022 May 11. Sci Transl Med. 2022. PMID: 35544595 Free PMC article.
-
Persistent muscle hyperalgesia after adolescent stress is exacerbated by a mild-nociceptive input in adulthood and is associated with microglia activation.Sci Rep. 2022 Oct 31;12(1):18324. doi: 10.1038/s41598-022-21808-x. Sci Rep. 2022. PMID: 36316425 Free PMC article.
References
-
- Abdelhamid RE, Kovacs KJ, Pasley JD, Nunez MG, Larson AA. Forced swim-induced musculoskeletal hyperalgesia is mediated by CRF2 receptors but not by TRPV1 receptors. Neuropharmacology 2013;72:29–37.
-
- Agudelo LZ, Femenía T, Orhan F, Porsmyr-Palmertz M, Goiny M, Martinez-Redondo V, Correia JC, Izadi M, Bhat M, Schuppe-Koistinen I, Pettersson AT, Ferreira DMS, Krook A, Barres R, Zierath JR, Erhardt S, Lindskog M, Ruas JL. Skeletal muscle PGC-1α1 modulates kynurenine metabolism and mediates resilience to stress-induced depression. Cell 2014;159:33–45.
-
- Airaksinen O, Brox JI, Cedraschi C, Hildebrandt J, Klaber-Moffett J, Kovacs F, Mannion AF, Reis S, Staal JB, Ursin H, Zanoli G. Pain O behalf of the CBWG on G for CLB. Chapter 4 European guidelines for the management of chronic nonspecific low back pain. Eur Spine J 2006;15:s192–300.
-
- Alexander JK, DeVries AC, Kigerl KA, Dahlman JM, Popovich PG. Stress exacerbates neuropathic pain via glucocorticoid and NMDA receptor activation. Brain Behav Immun 2009;23:851–60.
-
- Aloe L, Alleva E, Fiore M. Stress and nerve growth factor: findings in animal models and humans. Pharmacol Biochem Behav 2002;73:159–66.
MeSH terms
LinkOut - more resources
Full Text Sources
Miscellaneous