Hongyan Yang

Ms. Hongyan Yang

orcid

Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

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

Representative Publications

View All Publications
20 May 2022 in Cells
Verified
Journal Article
Open access
PDF file
GWGuiling Wu
Guiling Wu
YGYanjie Guo
Yanjie Guo
HYHongyan Yang
Hongyan Yang
CLChenhan Li
Chenhan Li
MTMiaomiao Tian
Miaomiao Tian
Feng GaoFeng Gao
Feng Gao
Long-term exercise-induced metabolic adaptations occupy a central position in exercise-afforded cardiac benefits. Emerging evidence suggests that branched-chain amino acid (BCAA) catabolic defect contributes to cardiac dysfunction in multiple cardiometabolic diseases. However, the role of BCAA catabolism in exercise-afforded cardiac benefits remains unknown. Here, we show that exercise improves BCAA catabolism and thus reduce cardiac vulnerability to myocardial ischemic injury. Exercise increased circulating BCAA levels in both humans (male adolescent athletes) and mice (following an 8-week swimming intervention). It increased the expression of mitochondrial localized 2C-type serine-threonine protein phosphatase (PP2Cm), a key enzyme in regulating BCAA catabolism, and decreased BCAA accumulation in mouse hearts, indicating an increase in BCAA catabolism. Pharmacological promotion of BCAA catabolism protected the mouse heart against myocardial infarction (MI) induced by permanent ligation of the left descending coronary artery. Although cardiac-specific PP2Cm knockout showed no significant effects on cardiac structural and functional adaptations to exercise, it blunted the cardioprotective effects of exercise against MI. Mechanistically, exercise alleviated BCAA accumulation and subsequently inactivated the mammalian target of rapamycin in MI hearts. These results showed that exercise elevated BCAA catabolism and protected the heart against myocardial ischemic injury, reinforcing the role of exercise in the promotion of cardiac health.

Verified
Journal Article
Open access
PDF file
MZMin Zhang
Min Zhang
HYHongyan Yang
Hongyan Yang
EYErwan Yang
Erwan Yang
JLJia Li
Jia Li
LDLing Dong
Ling Dong
Postprandial hyperglycemia is an important causative factor of type 2 diabetes mellitus, and permanent localization of intestinal GLUT2 in the brush border membrane is an important reason of postprandial hyperglycemia. Berberine, a small molecule derived from Coptidis rhizome, has been found to be potent at lowering blood glucose, but how berberine lowers postprandial blood glucose is still elusive. Here, we investigated the effect of berberine on intestinal glucose transporter 2 (GLUT2) translocation and intestinal glucose absorption in type 2 diabetes mouse model. Type 2 diabetes was induced by feeding of a high-fat diet and injection of streptozotocin and diabetic mice were treated with berberine for 6 weeks. The effects of berberine on intestinal glucose transport and GLUT2 translocation were accessed in isolated intestines and intestinal epithelial cells (IEC-6), respectively. We found that berberine treatment improved glucose tolerance and systemic insulin sensitivity in diabetic mice. Furthermore, berberine decreased intestinal glucose transport and inhibited GLUT2 translocation from cytoplasm to brush border membrane in intestinal epithelial cells. Mechanistically, berberine inhibited intestinal insulin-like growth factor 1 (IGF-1R) phosphorylation and thus reduced localization of PLC-β2 in the membrane, leading to decreased GLUT2 translocation. These results suggest that berberine reduces intestinal glucose absorption through inhibiting IGF-1R-PLC-β2-GLUT2 signal pathway.

27 February 2021 in Plant Foods for Human Nutrition
Verified
Journal Article
Closed access
PDF file
WLWenfeng Li
Wenfeng Li
MCMengting Cheng
Mengting Cheng
WZWentao Zhang
Wentao Zhang
RHRuiyan He
Ruiyan He
HYHongyan Yang
Hongyan Yang

1 February 2019 in Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
Verified
Journal Article
Closed access
JLJun Li
Jun Li
JXJie Xu
Jie Xu
Xinghua QinXinghua Qin
Xinghua Qin
HYHongyan Yang
Hongyan Yang
JHJuntao Han
Juntao Han
Feng GaoFeng Gao
Feng Gao

26 May 2023 in Nutrients
Verified
Journal Article
Open access
PDF file
WZWei Zhang
Wei Zhang
RSRongpei Shi
Rongpei Shi
TGTian Gao
Tian Gao
YHYang Hu
Yang Hu
JZJiaheng Zhou
Jiaheng Zhou
Feng GaoFeng Gao
Feng Gao
Peppermint essential oil, being natural and safe, with antioxidant and anti-inflammatory properties, has long been a research interest in relieving fatigue and improving exercise performance. However, the related studies report controversial results, and the mechanisms remain unclear. Here we found that inhalation of peppermint essential oil significantly extended the exhaustion time in rats subjected to 2-week weight-bearing swimming training. Sprague-Dawley rats were subjected to a 2-week weight-loaded forced swimming regimen. Prior to each swimming session, the rats were administered peppermint essential oil via inhalation. An exhaustive swimming test was performed at the end of the protocol. Rats treated with essential oil had significantly extended time to exhaustion compared with exercised rats without essential oil treatment. In addition, treated rats also showed reduced oxidative damage induced by endurance exercise. Notably, the rats receiving two-week essential oil inhalation while not subjected to swimming training did not show improved exercise performance. The findings demonstrate that repeated inhalation of peppermint essential oil enhances the effects of endurance training and improves exercise performance partially by preventing oxidative damage.

3 July 2023 in Food Chemistry: X
Verified
Journal Article
Open access
WLWenfeng Li
Wenfeng Li
WZWanjie Zhang
Wanjie Zhang
XFXin Fan
Xin Fan
HXHai Xu
Hai Xu
HYHong Yuan
Hong Yuan
HYHongyan Yang
Hongyan Yang
• FOS increases anthocyanins of red radish bioavailability. • Co-ingestion of FOS and ARR show higher antioxidant activity than ingestion alone. • FOS promotes anthocyanins hydrolyzing as anthocyanidins. • Bacteroides plays an important role in FOS increasing ARR bioavailability.