Objective To study intermediate and long term efficacy of uterine arterial embolization (UAE)with sodium alginate microspheres(KMG)at diameters 500-700μm in treatment of diffuse adenomyosis.Methods Totally 40 patients with standard difluse adenomyosis were enrolled and treated with UAE.KMG at diameters 500-700 μm for vascular embolization were used to embolize the arteries.The degree of dysmenorrhea,amount of menorrhea and uterine volume,as well as the level of serum CA125,follicle stimulating hormone(FSH),luteinizing hormone(LH),estradiol(E2)were investigated before andafter UAE.Results The follow up rates were 100%(40/40),100%(40/40),80%(32/40),68%(27/40),58%(23/40)after uterine arterial UAE 12,24,36,48 and 60 months respectively.The early,intermediate and long-term effective rates were 90%(36/40),88%(28/32),83%(19/23).The degree of dysmenorrhea,the amount of menorrhea and the uterine volume,as well as serum CA125 all decreased significantly 3 mouths after UAE at varying degrees(P＜0.05).Compared with other follow-up time,thedegree of dysmenorrhea and the amount of menorrhea declined to their lowest point at 6 month after UAE (P＜0.01).Paralleled with the decrease of volume of uterine,serum CA125 also decreased significantly and reached the lowest level 12 months later compared with other follow-up times(P＜0.01).Even at the 12th month after UAE serum CA125was not normal and FSH,LH and E2 did not change all the times after UAE(P>0.05).No recurrence was found during the 60 months after UAE.Condusion KMG used in UAE at diameters 500-700 μm has good intermediate and long term effectiveness in treatment of diffuse adenomyosis with no side effects.

This paper was focused on establishing a ICP-MS method with microwave digestion for simultaneous determination of lead, copper, arsenic, cadmium, mercury, magnesium, manganese, nickel, thallium in cassia tuckahoe capsule and its five raw herbal materials. Internal standard method was adopted to reduce matrix effect and other interference effects. The method established was shown to be simple with high sensitivity, strong specificity and good reproducibility. Linear relationship is good as R2 ≥ 0.999 3 while the average recovery was among 75.84% - 118.9%. The detection limit was 0.016 - 4.593 μg x L(-1). Data in this paper provided the basis for control of deleterious element in Guizhi Fuling capsules, and further more it was with referencing values for control of deleterious element in other crude drug.
Capsules ; Drugs, Chinese Herbal ; analysis ; Reproducibility of Results

Research on polymer impurities has always been important in the quality control of cephalosporins. Research on polymers in cephalosporins that lack active amino groups on the C-7 side chain has not been reported. Therefore, our study used cefazolin sodium, which is widely used in the clinic, as an example. The polymer in cefazolin sodium and its product "cefazolin sodium pentahydrate for injection" was analyzed by column switching liquid chromatography-high resolution mass spectrometry. Two polymer impurity peaks were detected and the possible structures of these polymers were suggested. Through two-dimensional liquid chromatography, the chromatographic peaks following Sephadex gel chromatography and high-performance gel chromatography were compared to those obtained by reverse high-performance liquid chromatography (HPLC) for cefazolin sodium as reported in the Chinese Pharmacopoeia. The HPLC method proves more suitable for polymer detection than Sephadex gel chromatography and high-performance gel chromatography. The method of polymer detection for cefazolin sodium was established using the method of related substances HPLC as described in the Chinese Pharmacopoeia.

OBJECTIVE: To discuss the coding of full dentition with 32 locations and measure the characteristics of some bony indexes in occlusal-facial digital radiology (DR). METHODS: To select randomly three hundred DR orthopantomogram and code the full dentition, then analyze the diversity of dental patterns. To select randomly one hundred DR lateral cephalogram and measure six indexes (N-S,N-Me,Cd-Gn,Cd-Go,NP-SN,MP-SN) separately by one odontologist and one trained forensic graduate student, then calculate the coefficient variation (CV) of every index and take a correlation analysis for the consistency between two measurements. RESULTS: (1) The total diversity of 300 dental patterns was 75%.It was a very high value. (2)All six quantitative variables had comparatively high CV value.(3) After the linear correlation analysis between two measurements, all six coefficient correlations were close to 1. This indicated that the measurements were stable and consistent. CONCLUSION The method of coding full dentition in DR orthopantomogram and measuring six bony indexes in DR lateral cephalogram can be used to forensic identification.
Cephalometry/methods* ; Facial Bones/diagnostic imaging* ; Female ; Forensic Dentistry ; Humans ; Image Processing, Computer-Assisted/methods* ; Jaw/diagnostic imaging* ; Male ; Radiography, Dental, Digital/methods* ; Radiography, Panoramic ; Tooth/diagnostic imaging*

Although gene therapy was regarded as a promising approach for glioma treatment, its therapeutic efficacy was often disappointing because of the lack of efficient drug delivery systems. Mesenchymal stem cells(MSCs) have been reported to have a tropism for brain tumors and thus could be used as delivery vehicles for glioma therapy. Therefore, in this study, we attempted to treat glioma by using MSCs as a vehicle for delivering replication-competent adenovirus. We firstly compared the infectivity of type 3, type 5, and type 35 fiber-modified adenoviruses in MSCs. We also determined suitable adenovirus titer in vitro and then used this titer to analyze the ability of MSCs to deliver replication-competent adenovirus into glioma in vivo. Our results indicated that type 35 fiber-modified adenovirus showed higher infectivity than did naked type 3 or type 5 fiber-modified adenovirus. MSCs carrying replication-competent adenovirus significantly inhibited tumor growth in vivo compared with other control groups. In conclusion, MSCs are an effective vehicle that can successfully transport replication-competent adenovirus into glioma, making it a potential therapeutic strategy for treating malignant glioma.
Adenoviridae ; Animals ; Brain Neoplasms ; pathology ; therapy ; Cell Line, Tumor ; Genetic Vectors ; Glioma ; pathology ; therapy ; Humans ; Mesenchymal Stem Cell Transplantation ; Mesenchymal Stromal Cells ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; Neoplasm Transplantation ; Oncolytic Virotherapy ; Random Allocation ; Virus Replication ; Xenograft Model Antitumor Assays

OBJECTIVETo explore the molecular mechanism and prevention of retinoic acid syndrome (RAS).

METHODSSDF-1 alpha mRNA from healthy adult lung tissue was measured by RT-PCR, CXCR4 protein expression on the cell membrane of APL cells induced by ATRA (APL-ATRA) was tested by FCM, and the rotary cell culture system (RCCS) was used to build a modal for in vitro stimulation of APL-ATRA infiltrating human lung tissue. The ability of APL-ATRA in adhesion, migration and infiltration was observed by interference from DEX, Ara-C and DNR.

RESULTSThe APL-ATRA cells could evidently infiltrate into normal lung tissue. Mean fluorescence intensity (MFI) of CXCR4 on the cell membrane of APL-ATRA cells was 30.6 +/- 1.8, which was much higher than that on unspecialized APL cells (9.8 +/- 4.2). SDF-1 alpha mRNA expression was detected positive in all 6 lung tissue. Contrary to the control groups, DEX could dramatically restrain the ability of APL-ATRA cells in adhesion and migration [(27.2 +/- 2.6)% vs. (46.0 +/- 3.0)%, (28.1 +/- 4.0)% vs. (48.2 +/- 3.0)%], while Ara-C and DNR could distinctly depress the ability in adhesion, migration and infiltration [(28.1 +/- 3.0)%, (30.2 +/- 3.2)% vs. (46.0 +/- 3.0)%; (29.0 +/- 4.0)%, (23.0 +/- 5.2)% vs. (48.2 +/- 3.0)%; (16.8 +/- 7.6)%, (17.1 +/- 6.0)% vs. (43.6 +/- 5.0)%].

CONCLUSIONIn vitro APL-ATRA cells can infiltrate into the human lung tissue. High expression of CXCR4 on APL-ATRA and SDF-1 alpha in the lung tissue may be one of the molecular mechanisms of the lung infiltration and RAS. DEX, Ara-C and DNR can dramatically restrain the ability of APL-ATRA cells in adhesion, migration and infiltration.

Adolescent ; Adult ; Cell Adhesion ; Cell Culture Techniques ; Cell Movement ; Chemokine CXCL12 ; genetics ; metabolism ; Child ; Female ; Humans ; Leukemia, Promyelocytic, Acute ; metabolism ; pathology ; Male ; Middle Aged ; Neoplasm Invasiveness ; Receptors, CXCR4 ; genetics ; metabolism ; Tretinoin ; adverse effects ; Tumor Cells, Cultured

To investigate the effect of cetirizine hydrochloride on the expression of neurokinin 1 receptor (NK-1R) and cytokines production induced by substance P (SP) in HaCaT cells (a human epidermal keratinocyte cell line) and dermal fibroblasts. The effect of cetirizine on the expression of NK-1R protein was detected by flow cytometry and Western blotting analysis. The modulation of cetirizine on the production of interferon (IFN)-gamma, interleukin (IL)-1beta, IL-6 and IL-8 in HaCaT cells and fibroblasts was measured by ELISA. The results showed that cetirizine significantly inhibited the expression of NK-1R in HaCaT cells and fibroblasts. SP induced the production of IFN-gamma, IL-1beta and IL-8 in both cell types. Cetirizine 1-100 micromol x L(-1) inhibited SP-induced IL-1beta and IL-8 production in HaCaT cells and fibroblasts, while had no effect on the production of IFN-gamma in both cells. Both SP and cetirizine had no effect on the secretion of IL-6 in HaCaT cells and fibroblasts. These findings suggest that cetirizine may be involved in the treatment of SP-induced skin inflammation by inhibiting the expression of substance P receptor and regulation the production of IL-1beta and IL-8 in epidermal keratinocyte and dermal fibroblasts.
Anti-Allergic Agents ; pharmacology ; Cell Line ; Cetirizine ; pharmacology ; Fibroblasts ; cytology ; metabolism ; Histamine H1 Antagonists, Non-Sedating ; pharmacology ; Humans ; Interferon-gamma ; metabolism ; Interleukin-1beta ; metabolism ; Interleukin-8 ; metabolism ; Keratinocytes ; cytology ; metabolism ; Receptors, Neurokinin-1 ; metabolism ; Substance P ; pharmacology

Objective To study the impact of adenoviral short hairpin RNA (shRNA) targeting phosphodiesterase 5 (PDE5 shRNA) on myo-cardial cells apoptosis at early stage post -myocardial infarction ( MI ).Methods MI was induced in mice by left coronary artery ligation.Mice were randomly assigned to test group [ n=10 , adenoviral vectors inserted with shRNA sequence for the inhibition of phosphodiesterase 5 ( PDE5 ) were injected intramyocardially to infarcted and border area ] and control group ( n =10 , injection with adenoviral vectors without therapeutic PDE5 shRNA ).One week post -MI, apoptosis was evaluated by TdT-mediated dUTP nick -end labeling ( TUNEL ) , proteins were extracted from the left ventricular of heart , level of PDE5 expression was detected using Western Bloting , the level of guanosine 3′, 5′-cyclic phosphate ( cGMP) or protein kinase G ( PKG) activity in the left ven-tricular of heart was evaluated by enzyme linked immunosorbent assay (ELISA).Results One week post -MI, compared to control group, test group had reduced number of apoptotic cells in infarct and periinfarct areas, and significantly reduced cardiomyocytes apoptosis in the periinfarct regions ( P<0.05 ).Compared to control group , the level of PDE5 was significantly decreased and the levels of cGMP and PKG were significantly increased in the test group ( P <0.05 ).Conclusion It the PDE5 shRNA has protective effect on acute myocardial infarction and significantly inhibit the apopto -sis of myocardial cell which may be closely related to the increased expression of cGMP and PKG .

Objective To study the protective effects of phosphodies terase 5 shRNA [PDE5shRNA] on doxorubicin (DOX)-induced cardiomyopathy in mice.Methods A single intraperitoneal injection of doxorubicin 15 mg · kg-1 to induce cardiomyopathy to establish model.Male 10-week-old C57BL/6J mice were randomly assigned to three groups:model group (n =16);experimental group(DOX + PDE5shRNA,n =16):a single intraperitoneal injection of same dose of doxorubicin and being simultaneously treated with a single myocardial injection of PDE5shRNA 1 x 1010 particles;Normal group (n =10):a single intraperitoneal injection of same volume of saline.After two weeks of administration,left ventricular end-systolic diameter (LVESD),left ventricular end-distolic diameter (LVEDD),left ventricular ejection fraction (LVEF) and percent fractional shortening (％ FS) were evaluated by echocardiography.Cardiac specimens were then subjected for HE (Hematoxyum Eosin),Masson staining,computing for each group of cardiac cell size and fibrosis area.Levels of cyclic guanosine monophosphate (cGMP) and protein kinase G (PKG) in the myocardium were assayed by ELISA.The expression of myosin heavy chain (MHC),Troponin I and Desmin were evaluated by Western blot.Results Two weeks later of administration,indicators in experimental group and model group were as follows:LVESD were(2.13 ±0.10),(2.75 ±0.12)mm;LVEDD were(2.98 ± 0.10),(3.42 ± 0.12) mm;LVEF were (58.74 ± 1.40)％,(48.53 ± 1.50)％;％ FS were (28.52 ± 2.10) ％,(19.59 ± 1.67) ％;the transverse diameter of cardiomyocytes were (14.68 ± 0.42),(13.75 ±0.38)μm;cardiac fibrosis were (2.28 ±0.20)％,(5.10 ±0.35)％;the levels of cGMP expression were (0.23 ± 0.02),(0.06 ± 0.01) pg · mg-1;the levels of PKG were (0.21 ± 0.02),(0.10 ± 0.01) pg · mg-1;the myocardial expression of MHC were 1.55 ± 0.16,1.15 ± 0.22;the expression of troponin I were 1.32 ± 0.08,0.88 ±0.08;the expression of Desmin were 1.327 ± 0.512,1.103 ± 0.038;all the above data were significantly different compared between two groups (all P ＜ 0.05).Conclusion The protective effects of PDE 5shRNA on doxorubicin-induced cardiomyopathy,mitigatting doxorubicin-induced impairment of cardiac function in mice,significantly attenuatting doxorubicin-induced atrophic degeneration of cardiomyocyte and myocardial fibrosis through possible activating cGMP/PKG signaling pathway.

Objective To study the significance of phosphatidyl inositol 3-kinase (PI3K) expression in amyotrophic lateral sclerosis (ALS) atrophy muscle fibers and investigate the pathogenesis of muscle fiber atrophy.Methods The clinical data of 90 ALS inpatients,admitted to our hospital from June 2005 to January 2013,were collected; and the features of clinical manifestations,creatine kinase level and electrophysiology were investigated.All patients accepted open muscle biopsy; the frozen tissues were performed histochemical,enzymology,anti-PI3K and nerve cell adhesion molecules (NCAM) monoclonal antibody immunohistochemistry staining; the pathological and ultrastructure characteristics were observed.Results A lot of small angular fibers,atrophy fibers and nuclear clump grouping were observed in skeletal muscle samples of ALS.PI3K positively expressed in sarcolemma of atrophy fibers,while NCAM negatively expressed.The pathologic changes of ultrastructure in transmission electromicroscope illustrated ALS atrophy fibers,having typical mitochondria paramorphia changes.Conclusion Mitochondria paramorphia changes and dysfunction are observed in ALS muscle fibers; atrophy fibers of ALS are related to muscle fiber apoptosis.