4.4 Article

Does analgesia and condition influence immunity after surgery? Effects of fentanyl, ketamine and clonidine on natural killer activity at different ages

Journal

EUROPEAN JOURNAL OF ANAESTHESIOLOGY
Volume 27, Issue 3, Pages 233-240

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/EJA.0b013e32832d540e

Keywords

age factors; analgesia; immune response; natural killer cells; surgery

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Background and objective Cellular immunity varies in the perioperative period. We evaluated the effects of fentanyl, clonidine and ketamine at different time points after surgery and in animals in different conditions ( young vs. old). Materials and methods Rats undergoing laparotomy under sevoflurane anaesthesia were assigned to receive saline, fentanyl (40 mu g kg(-1)), clonidine (10 mu g kg(-1)) or ketamine (10 mu g kg(-)1) 1 h before surgery. Natural killer (NK) activity was quantified at different time points ( immediately or after 18, 24, 48, 72 h and 8 days) in vitro by the lysis of YAC-1 cells. In-vivo assessment included counting the number of lung metastases induced by the MADB-106 cells. Results During the first 24 h after surgery, a rapid increase in NK activity was noted, followed by a significant depression returning to baseline at 8 days. Analgesics show specific effects: fentanyl depressed NK activity with or without surgery. Clonidine depressed NK activity in nonoperated animals and during the first 24 h after surgery. Ketamine depressed NK activity in nonoperated animals but, after surgery, this activity varied with the same time course as saline. Ketamine and clonidine significantly reduced the number of lung metastases in operated animals. Ketamine significantly reduced the number of metastases in old nonoperated animals. Finally, ageing has a significant negative influence. Conclusion Surgery, analgesics and co-existing conditions significantly influence cellular immunity. The importance of these changes varies with time. Fentanyl had a worse influence than clonidine and ketamine, but seemed equally protective against the development of metastases. Eur J Anaesthesiol 2010; 27:233-240

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