Jin Wang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Jin Wang has a total of 29 co-authors. Here are the top co-authors by number of shared publications:
- Jiao Guo
Institute of Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, China; Key Laboratory of Glucolipid Metabolic Disorder, Ministry of Education, Guangzhou, China; Guangdong TCM Key Laboratory for Metabolic Diseases, Guangzhou, China; Guangdong Metabolic Diseases Research Center of Integrated Chinese and Western Medicine, Guangzhou 510006, China
3 shared publications - Zhengquan Su
Guangdong Engineering Research Center of Natural Products and New Drugs, Guangdong Provincial University Engineering Technology Research Center of Natural Products and Drugs, Guangdong Pharmaceutical University, Guangzhou 510006, China
3 shared publications Hua Cao
School of Chemistry and Chemical Engineering, Guangdong Pharmaceutical University, Zhongshan 528458, China Tel.: +86-20-3935-2067; Fax: +86-20-3935-2067
2 shared publicationsCuiting Zhi
Guangdong Engineering Research Center of Natural Products and New Drugs, Guangdong Provincial University Engineering Technology Research Center of Natural Products and Drugs, Guangdong Pharmaceutical University, Guangzhou, 510006, China
1 shared publication- Di Yang
Guangdong Engineering Research Center of Natural Products and New Drugs, Guangdong Provincial University Engineering Technology Research Center of Natural Products and Drugs, Guangdong Pharmaceutical University, Guangzhou 510006, China
1 shared publication Feng Peng
West China Hospital, Sichuan University
1 shared publication
Latest Publications
- Open Access
- 1 January 2020
- Published by IOP Publishing in IOP Conference Series: Materials Science and Engineering
- Vol. 730 (1) , 012011
Study on the Effect of Galacto-oligosaccharide (GOS) in Relieving Constipation and Defecating Feces Excretion
To explore the role of Galacto-oligosaccharide (GOS) in preventing constipation and promoting excretion of feces. The high, medium and low doses of GOS-1000-S (8.8g/kg, 4.4g/kg, 2.2g/kg) were administered orally to constipation mice for 7 days, and then we measured the propulsive rate of intestines, first defecation time, the number of feces particle and fecal weight in 5 hours. The results showed that GOS-1000-S can significantly promote the small bowel propulsion, shorten the first defecation time and increase the fecal weight number of fecal particle of constipation mice. These indicate that GOS has the effect of relieving constipation and defecating feces excretion. This study provided a basis for the development of GOS with constipation-relieving functions as a health supplement.
- 1 January 2020
- Published by IOP Publishing in IOP Conference Series: Materials Science and Engineering
- Vol. 730 (1) , 012011
Open AccessStudy on the Effect of Galacto-oligosaccharide (GOS) in Relieving Constipation and Defecating Feces Excretion
To explore the role of Galacto-oligosaccharide (GOS) in preventing constipation and promoting excretion of feces. The high, medium and low doses of GOS-1000-S (8.8g/kg, 4.4g/kg, 2.2g/kg) were administered orally to constipation mice for 7 days, and then we measured the propulsive rate of intestines, first defecation time, the number of feces particle and fecal weight in 5 hours. The results showed that GOS-1000-S can significantly promote the small bowel propulsion, shorten the first defecation time and increase the fecal weight number of fecal particle of constipation mice. These indicate that GOS has the effect of relieving constipation and defecating feces excretion. This study provided a basis for the development of GOS with constipation-relieving functions as a health supplement.
- Open Access
Beneficial Metabolic Effects of Chitosan and Chitosan Oligosaccharide on Epididymal WAT Browning and Thermogenesis in Obese Rats
Many anti-obesity chemicals have been withdrawn from the market due to serious adverse reactions, and the researchers have turned their attention to low-toxic natural products. Previous studies have demonstrated that chitosan (CTS) and chitosan oligosaccharide (COS) were low-toxic natural products for the use of weight loss. However, it is still unclear whether CTS and COS have positive effects on the thermogenesis. In this study, CTS and COS significantly reduced the weight gain of rats without affecting food intake and effectively inhibited adipose tissue hypertrophy and hyperplasia. Consistently, CTS and COS significantly increased the thermogenic capacity of obese rats induced by high-fat diet (HFD) and increased the expression of browning genes and proteins (UCP1, PGC1α, PRMD16, and ATF2) in white adipose tissue (WAT) and brown adipose tissue (BAT). In vitro, COS inhibited the formation of mature adipocytes and increased the expression of browning genes. In conclusion, COS and CTS was used to explore the function and mechanism on thermogenesis, and CTS and COS can increase the browning of WAT and the thermogenesis of BAT to inhibit obesity. This effect may be achieved by promoting the expression of browning and thermogenic genes, providing new ideas for the utilization of COS and CTS.
Open AccessBeneficial Metabolic Effects of Chitosan and Chitosan Oligosaccharide on Epididymal WAT Browning and Thermogenesis in Obese Rats
Many anti-obesity chemicals have been withdrawn from the market due to serious adverse reactions, and the researchers have turned their attention to low-toxic natural products. Previous studies have demonstrated that chitosan (CTS) and chitosan oligosaccharide (COS) were low-toxic natural products for the use of weight loss. However, it is still unclear whether CTS and COS have positive effects on the thermogenesis. In this study, CTS and COS significantly reduced the weight gain of rats without affecting food intake and effectively inhibited adipose tissue hypertrophy and hyperplasia. Consistently, CTS and COS significantly increased the thermogenic capacity of obese rats induced by high-fat diet (HFD) and increased the expression of browning genes and proteins (UCP1, PGC1α, PRMD16, and ATF2) in white adipose tissue (WAT) and brown adipose tissue (BAT). In vitro, COS inhibited the formation of mature adipocytes and increased the expression of browning genes. In conclusion, COS and CTS was used to explore the function and mechanism on thermogenesis, and CTS and COS can increase the browning of WAT and the thermogenesis of BAT to inhibit obesity. This effect may be achieved by promoting the expression of browning and thermogenic genes, providing new ideas for the utilization of COS and CTS.
- 31 July 2019
- Published by Springer Nature in European Journal of Clinical Microbiology & Infectious Diseases
- Vol. 38 (11) , 1987-1998
Connection between gut microbiome and the development of obesity
The potential role of the gut microbiota in various human diseases has attracted considerable attention worldwide. Here, we discuss the vital role of the intestinal microbiota in the development of obesity. First, we describe how the gut microbiota promotes fat accumulation. Additionally, a high-fat diet leads to structural instability among in the gut microbiota, further leading to an increase in endotoxins, which aggravates obesity. We then discuss how gut microbiota metabolites, including short-chain fatty acids and lipopolysaccharides, affect the host. Finally, we review several strategies for regulating the intestinal flora.
- 31 July 2019
- Published by Springer Nature in European Journal of Clinical Microbiology & Infectious Diseases
- Vol. 38 (11) , 1987-1998
Connection between gut microbiome and the development of obesity
The potential role of the gut microbiota in various human diseases has attracted considerable attention worldwide. Here, we discuss the vital role of the intestinal microbiota in the development of obesity. First, we describe how the gut microbiota promotes fat accumulation. Additionally, a high-fat diet leads to structural instability among in the gut microbiota, further leading to an increase in endotoxins, which aggravates obesity. We then discuss how gut microbiota metabolites, including short-chain fatty acids and lipopolysaccharides, affect the host. Finally, we review several strategies for regulating the intestinal flora.
- 4 November 2017
- Published by Springer Nature in International Journal of Clinical Oncology
- Vol. 23 (2) , 258-265
Monitoring the estimated glomerular filtration rate (eGFR) in patients with small-cell lung cancer during chemotherapy: equations based on serum creatinine or cystatin C?
This study compared the differences between the estimated glomerular filtration rate (eGFR) calculated by several equations based on serum creatinine (Scr) and cystatin C (CysC) concentrations for monitoring renal function in patients with small-cell lung cancer (SCLC) during chemotherapy.
- 4 November 2017
- Published by Springer Nature in International Journal of Clinical Oncology
- Vol. 23 (2) , 258-265
Monitoring the estimated glomerular filtration rate (eGFR) in patients with small-cell lung cancer during chemotherapy: equations based on serum creatinine or cystatin C?
This study compared the differences between the estimated glomerular filtration rate (eGFR) calculated by several equations based on serum creatinine (Scr) and cystatin C (CysC) concentrations for monitoring renal function in patients with small-cell lung cancer (SCLC) during chemotherapy.