1.Advance in applied anatomy of structure and thrombosis in the left atrial appendage
Jianling SHI ; Hua ZHONG ; Wu YIN
Journal of Medical Postgraduates 2016;29(10):1107-1110
Left atrial appendage ( LAA) arises from the left atrial free wall. It is the remnant of the original embryonic LA, distinct from the rest of the left atrium. It has a unique anatomical structure, physiological function, hemodynamic characteristics. LAA has complex surrounding structures, great variability, and close relation with thrombosis. This paper reviews the morphological and functional characteristics of LAA. Familiar with adjacent relationship of LAA and correlation between LAA and thrombus formation has important clinical significance that can reduce the risk of postoperative complications in interventional procedures, the incidence of car?dioembolic stroke, the clinical misdiagnosis on LAA thrombosis.
2.Attractin.
Shi-liang SHEN ; Gregory S BARSH ; Zhong-bi WU
Chinese Journal of Pathology 2005;34(7):429-431
Agouti Signaling Protein
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Animals
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Central Nervous System
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abnormalities
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metabolism
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pathology
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Energy Metabolism
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Hair Color
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genetics
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physiology
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Humans
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Intercellular Signaling Peptides and Proteins
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metabolism
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Membrane Proteins
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genetics
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metabolism
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physiology
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Mutation
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Obesity
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genetics
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metabolism
4.Effect of flunarizine on the epileptiform discharges in cortex and hippocampus of rat with penicillin induced epilepsy.
Guo-feng WU ; Shi-hai SHAN ; You-zhong DONG
Chinese Journal of Applied Physiology 2004;20(2):179-204
Animals
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Cerebral Cortex
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drug effects
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physiology
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Epilepsy
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chemically induced
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physiopathology
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Female
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Flunarizine
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pharmacology
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Hippocampus
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drug effects
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physiology
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Male
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Penicillins
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adverse effects
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Rats
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Rats, Wistar
6.Diagnosis realization of knee joint synovial chondromatosis:clinical data of 28 cases.
Qin-Zhong ZHANG ; Shi-Liang WU ; Shuang-Ming FEI ; Hua CAO ; Wu-Lin QI
China Journal of Orthopaedics and Traumatology 2012;25(8):694-696
OBJECTIVETo investigate diagnosis and therapeutic effects of knee joint synovial chondromatosis with arthroscopic.
METHODSFrom March 1995 to July 2011, 28 patients with knee joint synovial chondromatosis were treated. Among them, 18 males and 10 females ranging age from 25 to 81 (mean 55.2) years,the course of disease ranged from 0.5 to 15 (mean 5.6) years. Clinical manifestation mainly included pain, swell and functional limitation of knee joint. Knee open surgery (17 cases) and laparoscopic surgery (10 cases) were respectively used. Clinical symptom,image data,pathological manifestation and effects under arthroscopy were observed, Lysholm scoring was used to evaluate effects.
RESULTSAll patients were followed up except one lost, the duration ranging from 6 to 24 months. Lysholm score in knee open surgery was increased from (41.89 +/- 6.81) preoperatively to (67.73 +/- 7.62) postoperatively;while in laparoscopic surgery it was increased from (40.78 +/- 7.54) preoperatively to (77.46 +/- 8.43) postoperatively.
CONCLUSIONArthroscopic surgery, which has no risk of rupture of incision, nonunion, earlier to exercise, is a good method to diagnosis and treat knee joint synovial chondromatosis.
Adult ; Aged ; Aged, 80 and over ; Chondromatosis, Synovial ; diagnosis ; surgery ; Female ; Follow-Up Studies ; Humans ; Knee Joint ; surgery ; Laparoscopy ; Male ; Middle Aged ; Treatment Outcome
7.Selection of Monascus with High Yellow Pigment Production
Bo ZHOU ; Ju-Fang WANG ; Zhen-Qiang WU ; Shi-Zhong LIANG ;
Microbiology 2008;0(12):-
The Monascus mutant with high yield of yellow pigment was obtained by using conventional relevant mutation techniques, e.g., treating with physical mutagens(such as UV light) and chemical sub- stances (such as N-methyl-N'-nitro-N-nitrosoguanidine). The yellow pigment was scanned from 300 nm to 600 nm with UV spectrometer, the maximal absorption was determined at 410 nm. The growth characteristic of Monascus mutant is stable, the yellow pigment value and colour hue in liquid fermentation can reach 100 U/mL and 3.5 respectively. The yellow pigment is stable from pH 3 to pH 8, but the precipitation appeared as the pH of the pigment solution lower than 3.
8.Progress in the study of core-crosslinked polymeric micelles in drug delivery system.
Jing-Mou YU ; Jia-Zhong WU ; Xin-Shi WANG ; Yi JIN
Acta Pharmaceutica Sinica 2014;49(2):183-189
The core-crosslinked polymeric micelles were used as a new drug delivery system, which can decrease the premature drug release in blood circulation, improve the stability of the micelles, and effectively transport the drug into the therapy sites. Then the drug bioavailability increased further, while the side effect reduced. Most drugs were physically entrapped or chemically covalent with the polymer in the internals of micelles. Based on the various constitutions and properties of polymeric micelles as well as the special characteristics of body microenvironment, the environment-responsive or active targeting core-crosslinked micelles were designed and prepared. As a result, the drug controlled release behavior was obtained. In the present paper, the research progress of all kinds of core-crosslinked micelles which were published in recent years is introduced. Moreover, the characteristic and application prospect of these micelles in drug delivery system are analyzed and summarized.
Animals
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Antineoplastic Agents
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administration & dosage
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chemistry
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therapeutic use
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Cross-Linking Reagents
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chemistry
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metabolism
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Drug Carriers
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chemistry
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metabolism
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Humans
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Micelles
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Molecular Structure
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Neoplasms
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drug therapy
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Particle Size
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Pharmaceutical Preparations
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administration & dosage
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Polyethylene Glycols
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chemistry
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metabolism
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Polymers
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chemistry
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metabolism
9.Vascular endothelial growth factor in three-dimensional angiogenesis induced by rat tail collagen gel
Sen SHI ; Yanzheng HE ; Li SONG ; Yong LIU ; Hui YANG ; Wu ZHONG ; Hong ZENG
Chinese Journal of Tissue Engineering Research 2010;14(16):2879-2882
BACKGROUND: Angiogenesis attracts much attention in tissue engineering field. Previous research has proved that a two-dimensional culture of vascular endothelial growth factor (VEGF) promotes angiogenesis.OBJECTIVE: To evaluate the effect of VEGF on three-dimensional angiogenesis.METHODS: Endothelial progenitor cells were separated from the SD rat bone marrow. At about 70%-80% fusion, rat tail collagen gel was added to establish three-dimensional models. Samples in the experimental group were incubated in complete culture solution containing M199 culture media, fetal bovine serum, VEGF, and double antibody. The samples in the control group were incubated with VEGF-free culture media. In vitro culture and amplification of bone marrow-derived endothelial progenitor cells were determined at 1, 4, 7, and-20 days after incubation. Morphology and quantitative analysis were performed at 3, 6, 9, and 12 days after three-dimensional model establishment.RESULTS AND CONCLUSION: Endothelial progenitor cells grew from three-dimensional matrix into collagen matrix in the experimental group. Budding and infiltration were observed in the collagen within 24 hours, and branching-like structure was then gradually formed. Cells in the control group grew slowly, with slowing budding, small tubiform structure, superficial infiltration into COllagen, sparse network structure, and non-intact. Numbers of newborn vessels in the expedmental group were significantly greater than control group (P<0.01). A detection on gel block showed positive expressions of endothelin-1 and endothelial nitric oxide synthase-3 on the 3~(rd), 6~(th), 9~(th), and 12~(th) days. The results demonstrated that VEGF mobilized and induced endothelial progenitor cells in order to promote angiogenesis. Rat tail collagen gel induced endothelial progenitor cells which behaved migration, proliferation, and pullulation of angiogenesis.
10.Clinicopathological features of IgA nephropathy associated with malignant hypertension and their correlation to renal vascular lesions
Pu CHEN ; Xiangmei CHEN ; Yuansheng XIE ; Guangyan CAI ; Xuefeng SUN ; Suozhu SHI ; Jie WU ; Zhong YIN
Chinese Journal of Nephrology 2008;24(6):392-397
Objective To explore the clinicopathological features of IgA nephrolpathy associated with malignant hypertension (IgAN-MHT) and to analyze their correlation with renal vascular lesions. Methods Twenty-nine patients of IgAN-MHT were screened from 2000 biopsy-proven eases with primary IgA nephropathy (IgAN) in our department from April 1997 to May 2007. Data of clinicopathology and follow-up of these 29 patients were collected. Semi- quantitative analysis was performed to evaluate the pathological changes. Inner lumen, outer lumen, intimal thickness, tunica media-to-internal lumen ratio of 436 arterioles, 124 interlobular arteries and 5 arcuate arteries were measured. The primary endpeint was the composite of a doubling of serum creatinine level and ESRD. Correlations of renal vascular lesions with clinical manifestation, pathological change and prognosis were examined by Spearman and Cox methods. Results 1.5% of all the IgAN patients presented malignant hypertension. The common clinical features were renal failure (100%), hyperurieacidemia (62.7%) and hypertriglyceridemia (51.7%). The average amount of urine protein excretion was 2.8 g/d. The common pathological changes were moderate mesangial proliferation, severe global sclerosis, severe interstitial inflammation and severe interstitial- tubular fibrosis. The small arteries (arcuate arteries and interlobular arteries) and arterioles (afferent arterioles) were both involved in IgAN-MHT. The characteristic lesions of intrarenal arteries included vascular occlusion, media thickening, proliferative endarteritis (onionskin lesion, musculomucoid intimal hyperplasia), hyaline arteriosclerosis, but mainly vascular occlusion (86.2%). The arteriole lesion was negatively correlated with age and total protein level; vascular occlusion was positively correlated with uric acid level. The average foUow-up period was 21.1 months. Forteen patients reached the endpoint. The arteriole lesion was the main independent risk factor for the progression of IgAN-MHT (RR=10.21, 95%CI=1.16~89.67). Conclusions The main clinical feature of IgAN-MHT is renal failure. The main histological feature of intrarenal vascular lesions is occludes arterioles. Arteriole lesion is the main independent risk factor for the progression of IgAN-MHT.