Li Wei, Tang Hui-Zhen, Jiang Yan-Bo, Xu Mei-Xi
Department of Anesthesiology, Cancer Center, Sun Yat-sen University, Guangzhou, Guangdong, PR China.
Ai Zheng. 2003 Jun;22(6):634-6.
BACKGROUND & OBJECTIVE: Morphine has been proved to inhibit human immune system, and large dose of fentanyl also decrease the activation of natural killer cells. This study was designed to investigate the effects of different doses of fentanyl on T-lymphocyte subpopulations and natural killer cells during esophageal cancer surgery under general anesthesia.
Forty-five patients with esophageal cancer were randomly divided into 3 groups (I, II,III) with 15 cases in each group respectively. The doses of fentanyl in three groups were 5, 10, and 20 microg/kg, respectively. Central venous blood samples (6 ml) were collected before anesthesia, 24 hours and 48 hours after the operation, respectively. Monoclonal antibodies assay was used to identify T cells and NK cells.
The counts of CD3(+) (T%) (Group I 50.30+/-8.42, Group II 48.53+/-9.62, GroupIII 46.58+/-8.56), CD4(+) (T%) (Group I 30.04+/-7.24, Group II 28.67+/-7.52, Group III 26.65+/-6.55),and NK cells (Group I 3.26+/-1.62, Group II 3.01+1.56, GroupIII 3.01+/-1.54) in three groups decreased significantly at 24 hours after surgery (P< 0.01). The decrease at 48 hours after surgery were more significant in groupIII (CD3(+) 48.89+/-9.82, CD4(+) 22.64+/-6.02, NK Cells 3.41+/-1.88) than in group I(CD3(+) 57.32+/-9.13, CD4(+) 35.62+/-5.98, NK cells 5.96+/-1.08) and group II(CD3(+) 55.62+/-10.21, CD4(+) 34.24+/-6.85, NK cells 6.04+/-1.09) (P< 0.05). There was no statistical significance in the counts of CD3(+), CD4(+), and NK cells between the time of 48 hours after the operation and preoperation in group I and group II.
Fentanyl, as a kind of opiate drug, could contribute to the immunosuppression, and large-dose fentanyl administration would be more effective in suppression of immunity function than small dose fentanyl.
已证实吗啡可抑制人体免疫系统,大剂量芬太尼也会降低自然杀伤细胞的活性。本研究旨在探讨全身麻醉下食管癌手术期间不同剂量芬太尼对T淋巴细胞亚群和自然杀伤细胞的影响。
45例食管癌患者随机分为3组(I组、II组、III组),每组15例。3组芬太尼剂量分别为5、10和20μg/kg。分别于麻醉前、术后24小时和48小时采集中心静脉血样本(6ml)。采用单克隆抗体检测法鉴定T细胞和NK细胞。
术后24小时,3组CD3(+)(T%)(I组50.30±8.42,II组48.53±9.62,III组46.58±8.56)、CD4(+)(T%)(I组30.04±7.24,II组28.67±7.52,III组26.65±6.55)及NK细胞(I组3.26±1.62,II组3.01±1.56,III组3.01±1.54)计数均显著下降(P<0.01)。术后48小时,III组(CD3(+) 48.89±9.82,CD4(+) 22.64±6.02,NK细胞3.41±1.88)下降幅度大于I组(CD3(+) 57.32±9.13,CD4(+) 35.62±5.98,NK细胞5.96±1.08)和II组(CD3(+) 55.62±10.21,CD4(+) 34.24±6.85,NK细胞6.04±1.09)(P<0.05)。I组和II组术后48小时与术前CD3(+)、CD4(+)及NK细胞计数差异无统计学意义。
芬太尼作为一种阿片类药物可导致免疫抑制,大剂量芬太尼比小剂量芬太尼对免疫功能的抑制作用更强。