Differential impact of psychological and psychophysical stress on low back pain in mice

• Verfasst von: La Porta, Carmen [VerfasserIn]
• Verfasst von: Tappe-Theodor, Anke [VerfasserIn]
• Titel: Differential impact of psychological and psychophysical stress on low back pain in mice
• Verf.angabe: Carmen La Porta, Anke Tappe-Theodor
• E-Jahr: 2020
• Jahr: February 27, 2020
• Umfang: 17 S.
• Fussnoten: Gesehen am 23.07.2020
• Titel Quelle: Enthalten in: Pain
• Ort Quelle: New York, NY [u.a.] : Lippincott Williams and Wilkins, 1975
• Jahr Quelle: 2020
• Band/Heft Quelle: 161(2020), 7, Seite 1442-1458
• ISSN Quelle: 1872-6623
• DOI: doi:10.1097/j.pain.0000000000001850
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: Astrocyte
• Sach-SW: dorsal-horn neurons
• Sach-SW: Hypersensitivity
• Sach-SW: induced mechanical hyperalgesia
• Sach-SW: induced musculoskeletal
• Sach-SW: inflammatory cytokines
• Sach-SW: Low back pain
• Sach-SW: Microglia
• Sach-SW: muscle
• Sach-SW: Muscle
• Sach-SW: nerve growth-factor
• Sach-SW: ngf
• Sach-SW: Priming
• Sach-SW: Psychological stress
• Sach-SW: Psychophysical stress
• Sach-SW: rat model
• Sach-SW: Referred pain
• Sach-SW: restraint stress
• Sach-SW: sensory neurons
• Sach-SW: Spinal cord
• Sach-SW: spinal-cord
• K10plus-PPN: 1725391589

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.