دورية أكاديمية

Chitosan promotes immune responses, ameliorates glutamic oxaloacetic transaminase and glutamic pyruvic transaminase, but enhances lactate dehydrogenase levels in normal mice in vivo

التفاصيل البيبلوغرافية
العنوان: Chitosan promotes immune responses, ameliorates glutamic oxaloacetic transaminase and glutamic pyruvic transaminase, but enhances lactate dehydrogenase levels in normal mice in vivo
المؤلفون: Yeh, Ming-Yang, Shih, Yung-Luen, Chung, Hsueh-Yu, Chou, Jason, Lu, Hsu-Feng, Liu, Chia-Hui, Liu, Jia-You, Huang, Wen-Wen, Peng, Shu-Fen, Wu, Lung-Yuan, Chung, Jing-Gung
المساهمون: Cheng Hsin Gen Hosp, Off Director, Fu Jen Catholic Univ, Dept Sch Med, Shin Kong Wu Ho Su Mem Hosp, Dept Pathol & Lab Med, Taipei Med Univ, Sch Med Lab Sci & Biotechnol, Jen Teh Jr Coll Med Nursing & Management, Cheng Hsin Gen Hosp, Dept Anat, Cheng Hsin Gen Hosp, Dept Clin Pathol, Chia Nan Univ Pharm & Sci, Ctr Gen Educ, China Med Univ, Dept Biol Sci & Technol, I Shou Univ, Sch Chinese Med Post Baccalaureate, Yanchao Campus,8 Yida Rd, Asia Univ, Dept Biotechnol
بيانات النشر: Spandidos Publ Ltd
سنة النشر: 2016
المجموعة: Chia Nan University of Pharmacy & Science Institutional Repository (CHNAIR)
مصطلحات موضوعية: chitosan, immune responses, glutamic oxaloacetic transaminase, glutamic pyruvic transaminase, lactate dehydrogenase
الوصف: Chitosan, a naturally derived polymer, has been shown to possess antimicrobial and anti-inflammatory properties; however, little is known about the effect of chitosan on the immune responses and glutamic oxaloacetic transaminase (GOT), glutamic pyruvic transaminase (GPT) and lactate dehydrogenase (LDH) activities in normal mice. The aim of the present study was to investigate whether chitosan has an effect on the immune responses and GOT, GPT and LDH activities in mice in vivo. BALB/c mice were divided into four groups. The negative control group was treated with a normal diet; the positive control group was treated with a normal diet plus orally administered acetic acid and two treatment groups were treated with a normal diet plus orally administered chitosan in acetic acid at doses of 5 and 20 mg/kg, respectively, every other day for 24 days. Mice were weighed during the treatment, and following the treatment, blood was collected, and liver and spleen samples were isolated and weighted. The blood samples were used for measurement of white blood cell markers, and the spleen samples were used for analysis of phagocytosis, natural killer (NK) cell activity and cell proliferation using flow cytometry. The results indicated that chitosan did not markedly affect the body, liver and spleen weights at either dose. Chitosan increased the percentages of CD3 (T-cell marker), CD19 (B-cell marker), CD11b (monocytes) and Mac-3 (macrophages) when compared with the control group. However, chitosan did not affect the phagocytic activity of macrophages in peripheral blood mononuclear cells, although it decreased it in the peritoneal cavity. Treatment with 20 mg/kg chitosan led to a reduction in the cytotoxic activity of NK cells at an effector to target ratio of 25: 1. Chitosan did not significantly promote B-cell proliferation in lipopolysaccharide-pretreated cells, but significantly decreased T-cell proliferation in concanavalin A-pretreated cells, and decreased the activity of GOT and GPT compared with that in the acetic ...
نوع الوثيقة: article in journal/newspaper
وصف الملف: 103 bytes; text/html
اللغة: English
تدمد: 1792-0981
1792-1015
العلاقة: Experimental and Therapeutic Medicine, v.11 n.4, pp.1300-1306; https://ir.cnu.edu.tw/handle/310902800/30970Test; https://ir.cnu.edu.tw/bitstream/310902800/30970/-1/30970.pdfTest; https://ir.cnu.edu.tw/bitstream/310902800/30970/1/index.htmlTest
DOI: 10.3892/etm.2016.3057
الإتاحة: https://doi.org/10.3892/etm.2016.3057Test
https://ir.cnu.edu.tw/handle/310902800/30970Test
https://ir.cnu.edu.tw/bitstream/310902800/30970/-1/30970.pdfTest
https://ir.cnu.edu.tw/bitstream/310902800/30970/1/index.htmlTest
رقم الانضمام: edsbas.5490216C
قاعدة البيانات: BASE
الوصف
تدمد:17920981
17921015
DOI:10.3892/etm.2016.3057