Augmentation of NK-cell activity and immunity by combined natural polyphenols and saccharides in vitro and in vivo

被引:0
|
作者
Park, Young Mi [1 ,2 ]
Lee, Hak Yong [1 ]
Shin, Dong Yeop [1 ]
Kim, Suk Hun [3 ]
Yoo, Yeol [3 ]
Kim, Min Ji [3 ]
Kim, Min Jung [4 ]
Yang, Hye Jeong [4 ]
Park, Kwang-Hyun [5 ,6 ,7 ,8 ]
机构
[1] INVIVO Co Ltd, Nonsan 32992, South Korea
[2] Wonkwang Univ, Coll Korean Med, Dept Pathol, Iksan 54651, South Korea
[3] Agr Corp Co Nongjeongsim LC, Jeonju 55070, South Korea
[4] Korea Food Res Inst, Wonju 55365, South Korea
[5] Nambu Univ, Dept Emergency Med Rescue, Gwangju 62271, South Korea
[6] Nambu Univ, Dept Oriental Pharmaceut Dev, Gwangju 62271, South Korea
[7] Chonnam Natl Univ, Dept Emergency Med, Gwangju 61469, South Korea
[8] Chonnam Natl Univ, Biomed Sci Grad Program BMSGP, Gwangju 61469, South Korea
基金
新加坡国家研究基金会;
关键词
Curcuma longa and Sargassum coreanum extract mixture; NK-cell activity; Cyclophosphamide-induced immunodeficient model; CURCUMA-LONGA; ACTIVATION; IMMUNODEFICIENCY; DIFFERENTIATION; POLYSACCHARIDE; SYSTEM;
D O I
10.1016/j.ijbiomac.2024.131908
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Curcuma longa and Sargassum coreanum are commonly used in traditional pharmaceutical medicine to improve immune function in chronic diseases. The present study was designed to systematically elucidate the in vitro and in vivo immuno-enhancing effects of a combination of C. longa and S. coreanum extracts (CS) that contain polyphenols and saccharides as functional molecules in a cyclophosphamide (Cy)-induced model of immunosuppression. In primary splenocytes, we observed the ameliorative effects of CS on a Cy-induced immunosuppression model with low cytotoxicity and an optimal mixture procedure. CS treatment enhanced T- and B-cell proliferation, increased splenic natural killer-cell activity, and restored cytokine release. Wistar rats were orally administered low (30 mg/kg), intermediate (100 mg/kg), or high (300 mg/kg) doses of CS for four weeks, followed by oral administration of Cy (5 mg/kg) for four weeks. Compared with the vehicle group, low-, intermediate-, and high-dose CS treatment accelerated dose-dependent recovery of the serum level of tumor necrosis factor-alpha, interferon-gamma, interleukin-2, and interleukin-12. These results suggest that CS treatment accelerates the amelioration of immune deficiency in Cy-treated primary splenocytes and rats, which supports considering it for immunity maintenance. Our findings provide experimental evidence for further research and clinical application in immunosuppressed patients.
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页数:9
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