Yu Sun

Dr. Yu Sun

orcid

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

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

Representative Publications

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22 July 2022 in Cell Proliferation
Verified
Journal Article
Open access
ZWZejing Wang
Zejing Wang
HLHao Lu
Hao Lu
TTTao Tang
Tao Tang
LLLei Liu
Lei Liu
BPBohan Pan
Bohan Pan
SZShiHui Zhu
ShiHui Zhu
Objectives: To determine the therapeutic effect of tetrahedral framework nucleic acids (tFNAs) on diabetic wound healing and the underlying mechanism.Materials and Methods: The tFNAs were characterized by polyacrylamide gel electrophoresis (PAGE), atomic force microscopy (AFM), transmission electron microscopy (TEM), dynamic light scattering (DLS) and zeta potential assays. Cell Counting Kit‐8 (CCK‐8) and migration assays were performed to evaluate the effects of tFNAs on cellular proliferation and migration. Quantitative polymerase chain reaction (Q‐PCR) and enzyme‐linked immunosorbent assay (ELISA) were used to detect the effect of tFNAs on growth factors. The function and role of tFNAs in diabetic wound healing were investigated using diabetic wound models, histological analyses and western blotting.Results: Cellular proliferation and migration were enhanced after treatment with tFNAs in a high‐glucose environment. The expression of growth factors was also facilitated by tFNAs in vitro. During in vivo experiments, tFNAs accelerated the healing process in diabetic wounds and promoted the regeneration of the epidermis, capillaries and collagen. Moreover, tFNAs increased the secretion of growth factors and activated the Wnt pathway in diabetic wounds.Conclusions: This study indicates that tFNAs can accelerate diabetic wound healing and have potential for the treatment of diabetic wounds.

1 May 2021 in Burns
Verified
Journal Article
Closed access
LHLunyang Hu
Lunyang Hu
BWBaoli Wang
Baoli Wang
YHYonggang Hong
Yonggang Hong
LXLong Xu
Long Xu
YJYong Jiang
Yong Jiang
YSYu Sun
Yu Sun

4 March 2009 in Critical Care
Verified
Journal Article
Open access
PDF file
YSYu Sun
Yu Sun
RYRui Yang
Rui Yang
JZJi-Gen Zhong
Ji-Gen Zhong
FFFeng Fang
Feng Fang
JJJin-Jin Jiang
Jin-Jin Jiang
JLJian Lu
Jian Lu
Introduction: Exogenous surfactant has been explored as a potential therapy for acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). In the present study, a nebuliser driven by oxygen lines found in the hospital was developed to deliver aerosolised porcine pulmonary surfactant (PPS). We hypothesised that aerosolised surfactant inhaled through spontaneous breathing may effectively reduce severe lung injury. Methods: Rats were intravenously injected with oleic acid (OA) to induce ALI and 30 minutes later they were divided into five groups: model (injury only), PPS aerosol (PPS-aer), saline aerosol (saline-aer), PPS instillation (PPS-inst), and saline instillation (Saline-Inst). Blood gases, lung histology, and protein and TNF-α concentrations in the bronchoalveolar lavage fluid (BALF) were examined. Results: The PPS aerosol particles were less than 2.0 μm in size as determined by a laser aerosol particle counter. Treatment of animals with a PPS aerosol significantly increased the phospholipid content in the BALF, improved lung function, reduced pulmonary oedema, decreased total protein and TNF-α concentrations in BALF, ameliorated lung injury and improved animal survival. These therapeutic effects are similar to those seen in the PPS-inst group. Conclusions: This new method of PPS aerosolisation combines the therapeutic effects of a surfactant with partial oxygen inhalation under spontaneous breathing. It is an effective, simple and safe method of administering an exogenous surfactant.

15 November 2021 in Frontiers in Medicine
Verified
Journal Article
Open access
BWBaoli Wang
Baoli Wang
WCWei Chenru
Wei Chenru
YJYong Jiang
Yong Jiang
LHLunyang Hu
Lunyang Hu
HFHe Fang
He Fang
XZXia Zhaofan
Xia Zhaofan
Objective: We conducted a systematic review and meta-analysis to comprehensively estimate the incidence and mortality of acute respiratory distress syndrome (ARDS) in overall and subgroups of patients with burns.Data sources: Pubmed, Embase, the Cochrane Library, CINAHL databases, and China National Knowledge Infrastructure database were searched until September 1, 2021.Study selection: Articles that report study data on incidence or mortality of ARDS in patients with burns were selected.Data extraction: Two researchers independently screened the literature, extracted data, and assessed the quality. We performed a meta-analysis of the incidence and mortality of ARDS in patients with burns using a random effects model, which made subgroup analysis according to the study type, inclusion (mechanical ventilation, minimal burn surface), definitions of ARDS, geographic location, mean age, burn severity, and inhalation injury. Primary outcomes were the incidence and mortality of burns patients with ARDS, and secondary outcomes were incidence for different subgroups.Data synthesis: Pooled weighted estimate of the incidence and mortality of ARDS in patients with burns was 0.24 [95% confidence interval (CI)0.2–0.28] and 0.31 [95% CI 0.18−0.44]. Incidences of ARDS were obviously higher in patients on mechanical ventilation (incidence = 0.37), diagnosed by Berlin definition (incidence = 0.35), and with over 50% inhalation injury proportion (incidence = 0.41) than in overall patients with burns. Patients with burns who came from western countries and with inhalation injury have a significantly higher incidence of ARDS compared with those who came from Asian/African countries (0.28 vs. 0.25) and without inhalation injury (0.41 vs. 0.24).Conclusion: This systematic review and meta-analysis revealed that the incidence of ARDS in patients with burns is 24% and that mortality is as high as 31%. The incidence rates are related to mechanical ventilation, location, and inhalation injury. The patients with burns from western countries and with inhalation injury have a significantly higher incidence than patients from Asian/African countries and without inhalation injury.Systematic Review Registration: identifier: CRD42021144888.

20 May 2025 in Advanced Healthcare Materials
Verified
Journal Article
Closed access
WLWei Li
Wei Li
JYJiahao Yang
Jiahao Yang
WKWeishi Kong
Weishi Kong
PFPeng Fan
Peng Fan
DGDingding Guan
Dingding Guan
YSYu Sun
Yu Sun

27 March 2021 in Respiratory Care
Verified
Journal Article
Closed access
PDF file
LHLunyang Hu
Lunyang Hu
BWBaoli Wang
Baoli Wang
YJYong Jiang
Yong Jiang
BZBanghui Zhu
Banghui Zhu
CWChen Wang
Chen Wang
YSYu Sun
Yu Sun
BACKGROUND: Until now, transfusion-related acute lung injury (TRALI) has been considered the leading cause of blood transfusion-related diseases and death. In addition, there is no clinically effective treatment plan for TRALI. The aim of this study was to systematically summarize the literature on risk factors for TRALI in critical patients. METHODS: Electronic searches (up to March 2020) were performed in the Cochrane Library, Web of Knowledge, Embase, and PubMed databases. We included studies reporting on the risk factors of TRALI for critical patients and extracted risk factors. A total of 13 studies met the inclusion criteria. RESULTS: We summarized and analyzed the potential risk factors of TRALI for critical patients in 13 existing studies. Host-related factors were age (odds ratio [OR] 1.16 [95% CI 1.08–1.24]), female sex (OR 1.26 [95% CI 1.16–1.38]), tobacco use status (OR 3.82 [95% CI 1.91–7.65]), chronic alcohol abuse (OR 3.82 [95% CI 2.97–26.83]), positive fluid balance (OR 1.24 [95% CI 1.08-1.42]), shock before transfusion (OR 4.41 [95% CI 2.38–8.20]), and American Society of Anesthesiologists (ASA) score of the recipients (OR 2.72 [95% CI 1.43–5.16]). The transfusion-related factors were the number of transfusions (OR 1.40 [95% CI 1.14–1.72]) and units of fresh frozen plasma (OR 1.21 [95% CI 1.01–1.46]). The device-related factor was mechanical ventilation (OR 4.13 [95% CI 2.20–7.76]). CONCLUSIONS: The risk factors that were positively correlated with TRALI in this study included number of transfusions and units of fresh frozen plasma. Age, female sex, tobacco use, chronic alcohol abuse, positive fluid balance, shock before transfusion, ASA score, and mechanical ventilation may be potential risk factors for TRALI. Our results suggest that host-related risk factors may play a more important role in the occurrence and development of TRALI than risk factors related to blood transfusions.