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首页> 外文期刊>World journal of gastroenterology : >Effect of antidepressants on body weight, ethology and tumor growth of human pancreatic carcinoma xenografts in nude mice.
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Effect of antidepressants on body weight, ethology and tumor growth of human pancreatic carcinoma xenografts in nude mice.

机译:抗抑郁药对裸鼠人胰腺癌异种移植物的体重,行为学和肿瘤生长的影响。

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AIM: To investigate the effects of mirtazapine and fluoxetine, representatives of the noradrenergic and specific serotonergic antidepressant (NaSSA) and selective serotonin reuptake inhibitor (SSRI) antidepressant respectively, on body weight, ingestive behavior, locomotor activity and tumor growth of human pancreatic carcinoma xenografts in nude mice. METHODS: A subcutaneous xenograft model of human pancreatic cancer cell line SW1990 was established in nude mice. The tumor-bearing mice were randomly divided into mirtazapine group (10 mg/kg per day), fluoxetine group (10 mg/kg per day) and control group (an equivalent normal saline solution) (7 mice in each group). Doses of all drugs were administered orally, once a day for 42 d. Tumor volume and body weight were measured biweekly. Food intake was recorded once a week. Locomotor activity was detected weekly using an open field test (OFT). RESULTS: Compared to the fluoxetine, mirtazapine significantly increased food intake from d 14 to 42 and attenuatedthe rate of weight loss from d 28 to 42 (t = 4.38, P 0.05). Compared to the control group, food intake was significantly suppressed from d 21 to 42 and weight loss was promoted from d 35 to 42 in the fluoxetine group (t = 2.52, P 0.05). There was a significant difference in body weight of the mice after removal of tumors among the three groups. The body weight of mice was the heaviest (13.66 +/- 1.55 g) in the mirtazapine group and the lightest (11.39 +/- 1.45 g) in the fluoxetine group (F( (2,12) ) = 11.43, P 0.01). The behavioral test on d 7 showed that the horizontal and vertical activities were significantly increased in the mirtazapine group compared with the fluoxetine and control groups (F( (2,18) ) = 10.89, P 0.01). These effects disappeared in the mirtazapine and fluoxetine groups during 2-6 wk. The grooming activity was higher in the mirtazapine group than in the fluoxetine group (10.1 +/- 2.1 vs 7.1 +/- 1.9 ) (t = 2.40, P 0.05) in the second week. There was no significant difference in tumor volume and tumor weight of the three groups. CONCLUSION: Mirtazapine and fluoxetine have no effect on the growth of pancreatic tumor. However, mirtazapine can significantly increase food intake and improve nutrition compared with fluoxetine in a pancreatic cancer mouse model.
机译:目的:探讨去甲肾上腺素能和特异性5-羟色胺能抗抑郁药(NaSSA)和选择性5-羟色胺再摄取抑制剂(SSRI)抗抑郁药米氮平和氟西汀对人胰腺癌异种移植物的体重,摄食行为,运动能力和肿瘤生长的影响在裸鼠中。方法:建立裸鼠人胰腺癌细胞株SW1990的皮下异种移植模型。荷瘤小鼠随机分为米氮平组(每天10 mg / kg),氟西汀组(每天10 mg / kg)和对照组(等效生理盐水)(每组7只小鼠)。每天口服42 d,所有药物的剂量都口服。每两周测量一次肿瘤体积和体重。每周记录一次食物摄入量。每周使用开放视野测试(OFT)检测运动能力。结果:与氟西汀相比,米氮平显着增加了食物摄入量,从第14天增加到42天,并使减肥率从第28天减少到42天(t = 4.38,P <0.05)。与对照组相比,氟西汀组的食物摄入量从d 21显着抑制到42 d,体重减轻从d 35促进到42 d(t = 2.52,P <0.05)。在三组中,去除肿瘤后小鼠的体重存在显着差异。米氮平组小鼠的体重最重(13.66 +/- 1.55 g),氟西汀组小鼠的最轻(11.39 +/- 1.45 g)(F((2,12))= 11.43,P <0.01 )。在第7天的行为测试表明,与氟西汀和对照组相比,米氮平组的水平和垂直活动明显增加(F((2,18))= 10.89,P <0.01)。在2-6周内,米氮平和氟西汀组的这些作用消失了。在第二周,米氮平组的梳理活性高于氟西汀组(10.1 +/- 2.1 vs 7.1 +/- 1.9)(t = 2.40,P <0.05)。三组的肿瘤体积和重量均无明显差异。结论:米氮平和氟西汀对胰腺肿瘤的生长没有影响。但是,在胰腺癌小鼠模型中,与氟西汀相比,米氮平可以显着增加食物摄入并改善营养。

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