Ching Yuan Hu

Prof. Ching Yuan Hu

University of Hawaiʻi at Mānoa, Honolulu, Hawaii, USA
orcid

Research Focus & Metrics

Academic Career Length

40Years (1987-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 October 2016 in Plant Foods for Human Nutrition
Verified
Journal Article
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YMYonghong Meng
Yonghong Meng
ASAnping Su
Anping Su
SYShuang Yuan
Shuang Yuan
HZHuaguo Zhao
Huaguo Zhao
STSiyuan Tan
Siyuan Tan
YGYurong Guo
Yurong Guo

1 May 2017 in Food Hydrocolloids
Verified
Journal Article
Closed access
WHWanyou Han
Wanyou Han
YMYonghong Meng
Yonghong Meng
CHChing Yuan Hu
Ching Yuan Hu
GDGuiru Dong
Guiru Dong
YQYuling Qu
Yuling Qu
YGYurong Guo
Yurong Guo

1 July 1993 in Comparative Biochemistry and Physiology Part A: Physiology
Verified
Journal Article
Closed access
ASA. Suryawan
A. Suryawan
CHChing Yuan Hu
Ching Yuan Hu

1 June 2017 in Biochemical and Biophysical Research Communications
Verified
Journal Article
Closed access
LHLianjie Hou
Lianjie Hou
JSJia Shi
Jia Shi
LCLingbo Cao
Lingbo Cao
GXGuli Xu
Guli Xu
CHChing Yuan Hu
Ching Yuan Hu
CWChong Wang
Chong Wang

19 July 2019 in Food & Function
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Journal Article
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SQShanshan Qi
Shanshan Qi
JHJia He
Jia He
HHHao Han
Hao Han
HZHongxing Zheng
Hongxing Zheng
HJHai Jiang
Hai Jiang
XLXinsheng Li
Xinsheng Li
Diabetic osteoporosis (DOP) is a systemic endocrine-metabolic osteopathy which has the characteristics of bone mineral density (BMD) reduction and bone microstructural destruction. Although anthocyanin-rich extract from black rice (AEBR) was reported to have a beneficial effect on diabetic rats, no studies have been performed on whether black rice anthocyanins are beneficial for diabetic osteoporosis. Therefore, in this study, a streptozotocin-induced diabetic rat model was established to investigate the protective effect of AEBR on diabetes-induced osteoporosis and its possible mechanism. AEBR at three doses (0.5, 1.0, and 2.0 g kg−1 d−1) were administered by oral gavage to diabetic rats for 8 weeks. The blood glucose, BMD, bone histomorphometry parameters, serum bone turnover biomarkers, bone marrow adipocyte numbers, as well as osteoprotegerin (OPG), runt-related transcription factor 2 (RUNX 2), and receptor activator of nuclear factor-κ B ligand (RANKL) protein expression in bone and serum were detected. The results indicated that AEBR dose-dependently decreased the blood glucose, increased the BMD, and decreased the serum bone turnover markers. The bone microstructure and osteoclast numbers in bone tissues returned to normal in the high AEBR dosage group; at the same time, the AEBR dose-dependently suppressed bone marrow adipogenesis. The RUNX 2 as well as the OPG/RANKL ratio in diabetic rats’ bone tissues increased significantly in the AEBR treatment group. Our results indicate that AEBR administration can ameliorate bone loss caused by diabetes; this is mainly attributed to its inhibition of bone turnover, suppression of bone marrow adipogenesis, and up-regulation of RUNX 2 and the OPG/RANKL expression ratio.

11 January 2021 in Journal of Agricultural and Food Chemistry
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Journal Article
Closed access
HHHao Han
Hao Han
CLCaifen Liu
Caifen Liu
WGWenchuan Gao
Wenchuan Gao
ZLZhongye Li
Zhongye Li
GQGongwei Qin
Gongwei Qin
CHChing Yuan Hu
Ching Yuan Hu