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Pain and inflammatory hyperalgesia induced by intradermal injections of human platelets and leukocytes
Author(s) -
Blunk J.,
Osiander G.,
Nischik M.,
Schmelz M.
Publication year - 1999
Publication title -
european journal of pain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.305
H-Index - 109
eISSN - 1532-2149
pISSN - 1090-3801
DOI - 10.1016/s1090-3801(99)90052-6
Subject(s) - platelet , hyperalgesia , erythema , medicine , anesthesia , intradermal injection , immunology , nociception , receptor
Acute and prolonged inflammatory processes, induced by intradermal injections of autologous platelet preparations, leukocytes, platelet‐leukocyte mixtures and vehicle solutions, were monitored in 20 human subjects for up to 48 h. Psychophysical methods were employed to assess the time course of pain response, and the development of hyperalgesia. Time course of the axon reflex erythema was analysed by computer based videography. Injections of functionally intact platelets [4.4 × 10 7 ± 0.6 × 10 7 in 50 μl (mean ± SEM)] caused distinct pain sensations [median pain rating 7.25 (25–75%: 6.5–7.5) on a scale form 0–10]. Both platelets injected through a microfilter (0.2 gm) and heat‐inactivated platelets induced similar initial pain response; however, pain duration was significantly shorter than for intact platelets. Control injections of leukocytes (5.4 × 106 ± 3.7 × 106 in 50 μl) and of vehicle solutions only caused minute pain sensations. Although platelet concentration in the mixture was only 50%, platelet/leukocyte mixtures produced axon reflex erythema that were significantly larger than those seen with naive platelets alone (11.1 ± 2.3 vs 8.3 ± 0.8 cm 2 ), Intact platelets and heat‐inactivated platelets both induced mechanical hyperalgesia and skin indurations at the injection site. Both reactions peaked between 6 and 24 h after the injection and disappeared within 48 h. Neither hyperalgesia, nor the development of indurations was noted at the injection sites of filtered platelets and vehicle solutions. Leukocyte injections induced hyperalgesia and indurations only in samples with a platelet contamination of more than 50 000 cells/μl. We conclude that platelets induce acute pain responses due to a soluble factor, whereas the development of hyperalgesia and the formation of indurations depends on a membrane‐bound factor. Moreover, platelets and leukocytes act synergistically in nociceptor activation.