Kaur Saini M, Nath Sanyal S
Department of Biophysics, Panjab University, Chandigarh, India.
Nutr Hosp. 2010 Jul-Aug;25(4):577-85.
Non steroidal anti inflammatory drugs (NSAIDs) are efficacious in chemoprevention of colorectal cancer. Therefore, the potential ability of Etoricoxib, a selective cycloxygenase-2(COX-2) inhibitor and Diclofenac, a preferential COX-2 inhibitor are considered in the chemoprevention of 1, 2-dimethylhydrazine (DMH) induced colon carcinogenesis in rat model. DMH was injected s.c. for six weeks while Etoricoxib and Diclofenac were fed daily orally alone and also in combination with an weekly subcutaneous injection of 1,2-dimethylhydrazine dihydrochloride (DMH) to the rats. After the treatment period of 6 weeks the animals were sacrificed by an overdose of ether anesthesia and the colonic tissues were removed and studied by the FTIR and NMR Spectroscopic techniques to evaluate the changes occurring in the lipid bilayer of colonic membrane lipids. The alterations in wave number of FTIR spectra as well as the chemical shifts of NMR spectra were recorded which signify the modulation of membrane lipids during colon carcinogenesis and possible cancer prevention by the oral administration of NSAIDs in an experimental model of chemical induced colon carcinogenesis.
非甾体抗炎药(NSAIDs)在结直肠癌的化学预防中具有疗效。因此,在大鼠模型中,研究了选择性环氧化酶-2(COX-2)抑制剂依托考昔和优先COX-2抑制剂双氯芬酸在化学预防1,2-二甲基肼(DMH)诱导的结肠癌发生中的潜在能力。将DMH皮下注射六周,同时将依托考昔和双氯芬酸单独每日口服给药,并且还与每周一次皮下注射盐酸1,2-二甲基肼(DMH)联合给予大鼠。在6周的治疗期后,通过过量乙醚麻醉处死动物,取出结肠组织,并用傅里叶变换红外光谱(FTIR)和核磁共振光谱(NMR)技术进行研究,以评估结肠膜脂质双层中发生的变化。记录FTIR光谱波数的变化以及NMR光谱的化学位移,这表明在化学诱导的结肠癌发生实验模型中,结肠致癌过程中膜脂质的调节以及口服NSAIDs可能的癌症预防作用。