Enlarged Areas of Pain and Pressure Hypersensitivityby Spatially Distributed Intramuscular Injections ofLow-Dose Nerve Growth Factor

•Distributed low-dose NGF injections induce pronounced muscle hypersensitivity•Distributed NGF injections affect a larger muscle area compared to single-bolus NGF•Low-dose NGF sensitize muscle nociceptors locally•Distributed NGF may mimic clinical pain better as a larger muscle area is affected Intr...

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Veröffentlicht in:The journal of pain 2019-05, Vol.20 (5), p.566-576
Hauptverfasser: Sørensen, Line B., Boudreau, Shellie A., Gazerani, Parisa, Graven-Nielsen, Thomas
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Sprache:eng
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Zusammenfassung:•Distributed low-dose NGF injections induce pronounced muscle hypersensitivity•Distributed NGF injections affect a larger muscle area compared to single-bolus NGF•Low-dose NGF sensitize muscle nociceptors locally•Distributed NGF may mimic clinical pain better as a larger muscle area is affected Intramuscular injection of nerve growth factor (NGF) causes muscle hyperalgesia without immediate pain. This double-blinded, randomized study assessed pain and muscle hypersensitivity after a single-site bolus NGF injection (5 µg) compared with 5 spatially distributed, low-dose NGF injections (1 µg, 4 cm distance) into the tibialis anterior (TA) muscles in 20 healthy subjects. Injection pain was rated on a visual analog scale. Reports of muscle pain with functional tasks (Likert scale score) and the presence of spontaneous pain were collected daily by using a diary. Pressure pain threshold (PPT), overall pain intensity (numerical rating scale), and pain areas following the TA contraction were collected at baseline; 3 hours; and 1, 3, 7, 14, and 21 days postinjection. Low immediate visual analog scale scores were associated with both injection protocols. Likert scale scores showed moderate pain intensities but no spontaneous pain, until day 12, for both injection protocols (P < .05). Reduced PPTs at the 5- and 1-µg injection sites were found after 3 hours, lasting until day 7 (P < .05). The 1-µg injection provoked decreased PPTs at day 1 (P = .036) at the proximal injection site and at day 1 (P = .02) and day 3 (P = .01) at the distal injection site. The TA muscle contraction resulted in larger pain areas and higher numerical rating scale scores at day 3 for the distributed injections compared with the single-site injection (P < .001). Perspective: Spatially distributed low-dose NGF injections induced prolonged pain, mechanical muscle hypersensitivity, and enlarged contraction-evoked pain areas. These features mirror some clinical muscle pain conditions in which diffuse pain areas and muscle hypersensitivity are present during the activities of daily living. Low-dose NGF injections may be useful for further studies of prolonged pain conditions.
ISSN:1526-5900
1528-8447
DOI:10.1016/j.jpain.2018.11.005