1.Role of hepatic sinusoids in lipopolysaccharide-induced liver injury
Lili ZHAO ; Dongya YUAN ; Fangyun SUN
Journal of Clinical Hepatology 2016;32(1):182-184
Endotoxin,which is also called lipopolysaccharide (LPS),is a unique element of Gram-negative bacteria.Liver is the main site for removing bacteria and endotoxin.Meanwhile,it is also the most vulnerable organ.Liver injury initially occurs in the hepatic sinu-soids.This article mainly introduces the impact of LPS on Kupffer cells,hepatic sinusoidal endothelial cells,oxidant/antioxidant balance in the hepatic sinusoids,and liver blood flow.It is believed that the function of hepatic sinusoids in LPS-induced liver injury should not be ig-nored,and the hepatic sinusoids would play an important role in the prevention and treatment of LPS-induced liver injury.
2.THE EFFECT OF SINOMENINE ON EXPERIMENTAL ARRHYTHMIA
Fangyun SUN ; Huiling GUO ; Xinkuan LI ; Al ET
Journal of Xi'an Jiaotong University(Medical Sciences) 1982;0(04):-
The effects of Sinomenine on experimental arrhythmia were studied. The result showed that Sinomenine could shorten the arrhythmetic period induced by picrotoxin in rabbit and protect rat against arrhythmia induced by BaCl_2. Sinomenine was found to recover the arrhythmia induced by BaCl_2-Ach into sinus rhythm in mice, Beside these Sinomenine also showed significant antagonising to ischemic arrhythmia.
3.Anomalous origin of the left coronary artery from the pulmonary artery in infants: depiction by 64 multi-slice spiral CT
Xiaomin DUAN ; Hua CHENG ; Ling JIANG ; Hui LIU ; Jiajin ZENG ; Fangyun WANG ; Guoqiang SUN
Chinese Journal of Radiology 2009;43(9):935-937
onary artery was turtuous and dilated in 4 cases. Conclusion 64 MSCT is emerging as an essential imaging tool for detecting early anomalous origin of the left coronary artery from the pulmonary artery with high resolution and significance.
4.Diagnosis and follow-up of patients with Kawasaki disease complicating coronary aneurysms by echocardiography: experience of 338 cases from a single center
Xuerui SUN ; Yan SUN ; Jiao YANG ; Xiaolin ZHANG ; Jingya LI ; Lanzhong JIN ; Fangyun WANG ; Li XUE ; Xin ZHANG ; Lin ZHENG ; Haiyan WEI ; Pei LI ; Ning MA
Chinese Journal of Ultrasonography 2018;27(2):139-142
Objective To investigate the diagnosis and prognosis of patients with coronary artery aneurysm in Kawasaki disease.Methods The data of ultrasonic diagnosis and follow-up of 338 children with Kawasaki disease complicated with coronary artery aneurysms were analyzed.Results The incidence of coronary artery aneurysm in the acute stage of Kawasaki disease was 21.2% (338/1 594).Of all the 338 cases,small aneurysms was 66.6% (225 cases),medium aneurysms was 25.1% (85 cases),and giant aneurysms was 8.3% (28 cases).There were 719 branches involved in 338 cases,32.8% of them in left main coronary artery and 31.1% in right coronary artery;25.3% in left anterior descending branch,and 10.8% in left circumflex branch.A total of 382 branches were followed up,including 218 branches of small coronary aneurysm group and 82.1% of them were completely recovered to the normal diameter.The medium aneurysm group was 124 brunches,the proportion of no significant change,retraction,and normal were 23.4%,68.5% and 8.1%,respectively.There were 40 brunches in the giant anuerysm group,in which the proportion of no significant change,retraction,and normal were 70.0%,27.5% and 2.5%,respectively.A total of 30 thrombosiswere detected by echocardiography in the acute stage,20 thrombosis were regularly followed up,12 thrombosis gradually subsided,and the other remained persist.Five thrombosis were detected in the sequelae stage,and all located in the giant coronary aneurysm.Seven children were clinically diagnosed with ischemic heart disease,of them,acute myocardial infarction in 1 case,1 died of heart failure.Conclusions Kawasaki disease coronary artery disease are common in small coronary aneurysms,of which the left main artery and right coronary artery lesions are the most common,and the prognosis is better;medium and giant aneurysm need more time to recovery,and are easy to complicated with thrombosis.
5.Echocardiographic and clinical retrospective study of 35 patients with Kawasaki disease combined with coronary artery thrombosis
Xiaolin ZHANG ; Zhongdong DU ; Lanzhong JIN ; Fangyun WANG ; Ning MA ; Xin ZHANG ; Guiqin MA ; Lin ZHENG ; Haiyan WEI ; Jingya LI ; Pei LI ; Yan SUN ; Jiao YANG
Chinese Journal of Applied Clinical Pediatrics 2017;32(21):1653-1656
Objective To summarize the echocardiographic findings and clinical characteristics of Kawasaki disease(KD) complicated with coronary artery thrombosis (CAT).Methods Thirty-five patients with KD combined with CAT were enrolled,who were admitted to Beijing Children's Hospital,Capital Medical University between July 2005 and August 2016.The clinical characteristics and echocardiographic findings during follow-ups were retrospectively studied.According to whether the childrenhad been complicated with myocardial ischemia,the patients were divided into 2 groups:ischemic group and non-ischemic group.The duration of fever,the time when the intravenous immunoglobulin(IVIG) was first injected,the time when coronary artery aneurysms (CAA) was formed,the maximum diameter of CAA and inflammatory index inthe acute phase were compared between 2 groups.Results All of the 35 children diagnosed as KD combined with CAT suffered firom CAA,and the coronary thrombosis was detected in all the cases with aneurysms.Thirty-five patients had 99 branches of CAA,of which the maximum diameter of CAA was (9.6 ± 3.1) mm(4.0-19.0 mm).Fifty-four plots of CAT were detected in the aneurysms.The diameter of CAA that thrombosis located was larger than that of which the thrombosis was not located[(10.9 ± 2.8) mm vs.(7.9 ± 2.6) mm],and the difference was significant(P <0.01).During 4 months to 10 years and 8 months [(39.2 ±29.5) months] follow-ups,CAA regressed in 32 branches [32.3% (32/99 branches)],of which 4 branches [4.0% (4/99 branches)] completely regressed to the normal diameter.The maximum diameter of CAA regressed was smaller than the maximum diameter of CAA consistence [(7.3 ± 1.9) mm vs.(10.6 ± 3.0) mm],and the difference was significant (P < 0.01).Out of 35 patients,15 cases [42.9% (15/35 cases) had myocardial ischemia,while the other 20 cases[57.2% (20/35 cases)] didn't have.Among 15 cases with myocardial ischemia,6 cases[17.1% (6/35 cases)] had myocardial infarction,4 cases [11.4% (4/35 cases)] had heart failure,and 1 case[2.9% (1/35 cases)] died of acute heart failure complicated with severe ventricular arrhythmia.Compared with non-ischemic group,the children in the ischemic group had longer duration of fever[(19.1 ± 7.8) d vs.(12.1 ± 3.3) d],higher white blood cell account in the acute phase[(24.8 ± 13.5) × 1012/L vs.(19.7 ±4.0) × 1012/L],later treatment of IVIG [(13.9 ± 5.5) d vs.(9.8 ±3.8) d],and earlier CAA formation [(16.0 ±4.9) d vs.(20.9 ± 14.5) d],and the differences were statistically significant (all P < 0.05).Conclusions CAT of children with KD commonly originates from CAA.Patients who have more serious inflammatory reaction in the acute phase,earlier formation,heavy severity and longer consistence of CAA are prone to have myocardial ischemia.Echocardiographic study plays an important role in monitoring CAA,detecting the CAT and finding the early left ventricle dysfunction,which is of clinical significance.
6.The value of echocardiography in the diagnosis of persistent fifth aortic arch and its classification
Lin ZHENG ; Fangyun WANG ; Xin ZHANG ; Yongli CAO ; Qun WU ; Guiqin MA ; Yan SUN ; Jingya LI ; Pei LI ; Ning MA
Chinese Journal of Ultrasonography 2020;29(10):857-863
Objective:To study the classification of persistent fifth aortic arch (PFAA) and the value of echocardiography in the diagnosis of PFAA.Methods:A total of 16 cases (male 6, female 10, at ages from 7 days to 4 years and 2 months old, the median age was 3 months) diagnosed with PFAA in Beijing Children′s Hospital Affiliated to Capital Medical University from January 2013 to June 2019 were studied retrospectively. The diagnosis standard, differential methods and misdiagnosed analysis of different subtypes of PFAA by echocardiography were summarized and analyzed.Results:The 16 cases included 1 case of type A1 double lumen aortic arch, 8 cases of type A2 single-lumen aortic arch, 3 cases of type B1 with pulmonary atresia and 4 cases of type B3 pulmonary artery branch arising from the distal end of ascending aorta. Only one patient of double lumen aortic arch missed diagnosis by echocardiography, and the rest were accurately diagnosed by echocardiography. CTA was performed in 13 cases, including 9 cases of type A, 1 case of type B1 and 3 cases of type B3, which confirmed the echocardiography diagnosis. Seven cases of Type A2 were operated.Conclusions:PFAA is a rare and complicated aortic arch malformation, which is divided into four major classification and multiple subtypes. Echocardiography can diagnose the PFAA and its classification, it is of great clinical significance for the early diagnosis, treatment and prognosis of children.