1.Through left subclavian vein emergent cardiac pacing guided by "three-peint measurement" method
Hui REN ; Junkang ZHANG ; Jie GONG ; Bo YUAN ; Hai LU ; Lanyan QU
Chinese Journal of General Practitioners 2009;8(3):189-190
Seventy eight patients who need bedside temporary cardiac pacing through left subclavian vein were divided into 2 groups. In group A (n=40) the "three-point measurement" method was applied: a was set for puncture point of left subclavian vein, b was the middle point of angulus sterni, c was the right edge of the sternum at the 4th intercostal space, the length of ab + bc was used to estimate the depth of right atrium for electrode to reach until the success of right ventricular pacing. In group B (n=38) the puncture to the right or the left subclavian vein for temporary pacing was performed with X-ray guidance in catheter lab. Total rescuing time, procedure time and the threshold voltage of cardiac pacing was recorded in each groups. All cases were successful paced without complication related emergency cardiac pacing with a successful rate of 100% in both groups. There was not difference between two groups in the procedure time and the threshold voltage of cardiac pacing (P > 0. 05). The total rescuing time of A group was (10.0± 2.2) min, and that of B group was (30.5±3.5) min (P<0.01). The average depth of the electrode was ab + bc +9.0 cm. The results suggest that "three-point measurement" method is valuable in the guiding of bedside emergent cardiac pacing through the left subclavian vein.
2.Clinical observation of Gingko biloba extract injection in treating early diabetic nephropathy.
Chinese journal of integrative medicine 2005;11(3):226-228
OBJECTIVETo observe the effect of Ginkgo biloba extract injection (GB) in treating early diabetic nephropathy (DN).
METHODSSixty DN patients were divided into two groups, the treated group were treated by GB and Western medicine, and the control group were given Western medicine alone. The study lasted for 4 weeks. Fasting plasma glucose (FPG), blood pressure, 24 h urinary albumin excretion (UAE), endogenous creatinine clearance rate (Ccr), blood lipids and hemorheology indices were examined before and after the study.
RESULTSCompared with the control group, UAE were significantly decreased (P < 0.01); Ccr, blood lipids and hemorheology indices were all improved after treatment in the treated group (P < 0.05 or P < 0.01). But in FPG and blood pressure there was no significant change between the treated group and the control group (P > 0.05).
CONCLUSIONGB is effective in treating early DN through decreasing urinary albumin excretion rate, regulating blood lipids, improving renal function and hemorheology.
Aged ; Diabetic Neuropathies ; drug therapy ; Female ; Ginkgo biloba ; Humans ; Infusions, Intravenous ; Male ; Middle Aged ; Phytotherapy ; Plant Extracts ; administration & dosage ; Treatment Outcome
3.Study on preventive and therapeutic effects of combined application of yindanxinnaotong soft capsule and exercise on atherosclerotic rats.
Jian-Lu WANG ; Lan WANG ; Long CHENG ; Xiao-Jie YIN ; Hai-Yu XU ; Wan-Dan WANG ; Ri-Xin LIANG
China Journal of Chinese Materia Medica 2014;39(13):2547-2552
To explore the prevention effect of the joint combination of Yindanxinnaotong soft capsule (YDXNT) and exercise (swimming) on atherosclerotic rats. The method of 3 x 3 factorial design, including two factors (YDXNT and swimming) and three levels (0, 1, 2 g x kg(-1) YDXNT; 0, 0.5, 1 h swimming), was mainly adopted. The atherosclerotic rat model was established by ligating their left common carotid arteries and feeding high-fat diet. After 8 weeks, blood samples were collected from their thoracic aorta to determine blood viscosity, plasma viscosity, fibrinogen (FIB), nitric oxide (NO), 6-keto-PGF(1alpha) endothelin (ET) and thromboxane B2 (TXB2). The tissues of left common carotid arteries of the rats were collected to detect the positive expression of SM22alpha and determine the semi-quantitation through the immunohistochemical staining. The result showed that the combination of YDXNT and swimming can significantly decrease the plasma viscosity (F = 3.241, P = 0.017), the high and low shear blood viscosity (F = 6.444, P = 0.001; F = 3.002, P = 0.024) and FIB (F = 4.046, P = 0.005). The increased NO and 6-keto-PGF(1alpha) and the decreased ET and TXB2 indicated a significant interaction (P < 0.05). The swimming showed an obvious main effect in the expression of up-regulated protein SM22alpha (F = 8.088, P = 0.001). The study suggested that the combined administration of YDXNT and swimming could improve the hemorheological parameters of atherosclerotic rats, protect the vascular endothelium, inhibit the vascular remodeling in atherosclerosis and positively prevent the atherosclerosis.
Animals
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Atherosclerosis
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drug therapy
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genetics
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metabolism
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prevention & control
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Blood Viscosity
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drug effects
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Combined Modality Therapy
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Drugs, Chinese Herbal
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administration & dosage
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Exercise Therapy
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Humans
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Male
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Microfilament Proteins
;
genetics
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metabolism
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Muscle Proteins
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genetics
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metabolism
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Rats
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Rats, Sprague-Dawley
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Swimming
4.Identification of six species of sarcosaphagous flies (Diptera) by sequence analysis of cytochrome oxidase subunit I gene (COI) in Weifang.
Xin-Jie WANG ; Xue-Hai WANG ; Li-Jiang DIAO ; Gui-Ping LU
Journal of Forensic Medicine 2006;22(2):93-94
OBJECTIVE:
To identify sarcosaphagous flies and their larvae, pupa.
METHODS:
Sarcosaphagous flies and their larvae, pupas were collected from human corpses and their surroundings in the Weifang city. A 304 bp region in COI gene was analyzed by mtDNA sequencing.
RESULTS:
The studied region showed no sequence divergence within same species and significant difference were found between different species in all samples.
CONCLUSION
It is a practical approach to identify these Sarcosaphagous flies and their larvae, pupas by sequence analysis of the 304bp region of the COI in mtDNA.
Animals
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Base Sequence
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China
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DNA Primers
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DNA, Mitochondrial/genetics*
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Diptera/genetics*
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Electron Transport Complex IV/genetics*
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Forensic Medicine
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Genes, Insect
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Humans
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Larva/genetics*
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Phylogeny
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Polymerase Chain Reaction/methods*
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Pupa/genetics*
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Sequence Analysis, DNA/methods*
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Species Specificity
5.Discussion on the Application of Cancerous Toxin Pathogenesis Theory in the Treatment of Gastric Cancer
Wei LU ; Zheng-Jie SHEN ; Hai-Bo CHENG
Journal of Nanjing University of Traditional Chinese Medicine 2016;32(2):101-103
ABSTRACT:China has a very high incidence of gastric cancer.Chinese medicine has advantages in the treating of gastric canc-er.Professor Zhou Zhong-yin,awarded National Chinese Medical Science Master,has put forward the theory of cancerous tox-in pathogenesis theory based on his long-term clinical experience.Better effect of the treatment of gastric cancer has been con-firmed by the application of cancerous toxin pathogenesis theory on gastric cancer patients.Cancerous toxin remaining in the stomach is the key pathogenesis of gastric cancer.Cancerous toxin always intermingled with phlegm turbidity,blood stasis, damp turbidity and toxic heat is very common in the patients with gastric cancer.So the principle and treatment of gastric canc-er is the combination of anti-cancer while removing toxic material and other therapeutic principle,such as regulating qi and har-monizing stomach,clearing heat and promoting diuresis,promoting blood circulation to remove blood stasis,reducing phlegm and resolving masses and reinforcing deficiency.
6.Restoration of erectile function by reconstructing cavernous nerves with small intestinal submucosa grafts.
Hong-Kai LU ; Hai-Jun ZHOU ; En-Jiang GAO ; Lu-Jie SONG ; Hai-Zhen ZUO ; Bo YAN ; Zhi-Yong YU ; Jing DU ; Wen-Hua BI
National Journal of Andrology 2010;16(2):150-153
OBJECTIVETo investigate the restoration of erectile function by reconstructing cavernous nerves (CN) with small intestinal submucosa (SIS) grafts.
METHODSWe prepared SIS grafts, established rat models and divided the models into a CN ablation, a sham-operation and an SIS graft group. The CNs at both sides were severed with 1 cm ablated in the first group, and 0.5 cm removed in the third, followed by reconstruction with the SIS grafts. Three months after surgery, the apomorphine test was performed to evaluate the erectile function, and then all the rats were sacrificed to detect the expression of nNOS in the penis.
RESULTSPenile erection was observed in 72.73% (8/11) of the rats for (1.07 +/- 0.89) times within 30 min in the SIS graft group, as compared with 0% (0/11) of the rats for (0.00 +/- 0.00) times in the CN ablation group (P < 0.01), and 90.91% (10/11) of the rats for (2.19 +/- 1.17) times in the sham-operation group (P < 0.01). The number of nNOS nerve fibers was significantly larger in the SIS graft than in the CN ablation group (70.36 +/- 10.09 versus 22.09 +/- 4.76, P < 0.01), but both were significantly smaller than that of the sham-operation group (90.81 +/- 5.69, P < 0.01).
CONCLUSIONThe SIS grafting technique contributes to the recanalization of the severed CN and restoration of erectile function in rats after surgical injury.
Animals ; Erectile Dysfunction ; surgery ; Intestinal Mucosa ; transplantation ; Intestine, Small ; Male ; Nerve Regeneration ; Nerve Tissue ; injuries ; surgery ; Penile Erection ; Penis ; innervation ; Rats ; Rats, Sprague-Dawley
7.Study on pharmacokinetics-pharmacodynamics correlation of Danshensu in rats with focal cerebral ischemia.
Jin-Chao AI ; Hui-Fen ZHOU ; Ming-Chun SHU ; Liu-Ling DAI ; Lu ZHENG ; Yu-Yan ZHANG ; Jie-Hong YANG ; Xian-Bin WU ; Hai-Tong WAN
China Journal of Chinese Materia Medica 2014;39(14):2751-2755
To study the pharmacokinetic process of Danshensu in cerebal ischemia injury model rats and the correlation with its anti-cerebral ischemia effect. In this study, the middle cerebral artery occlusion (MCAO) model was established, in which all of the rats were intravenously injected of Danshensu at a single dose of 40 mg x kg(-1). The HPLC-DAD method was applied to determine the plasma concentration of Danshensu at different time points and draw the drug-time curve. Meanwhile, the superoxide dismutase (SOD) and the lactate dehydrogenase (LDH) activity were determined to draw the time-effect curve. The DAS 3.2. 6 software was used to process the data, analyze their correlation, compare the pharmacokinetic difference between model and normal rats after the administration of the same doses of Danshensu and the changes in pharmacodynamic indicators of model rats after the administration, and evaluate the effect of Danshensu in treating the cerebral ischemia disease. According to the results, the pharmacokinetic processes of Danshensu in the cerebral ischemia-reperfusion and normal rats were consistent to the two-compartment model. The main pharmacokinetic parameters were: t1/2alpha were (0.267 +/- 0.026), (0.148 +/- 0.020) h;t1/2beta were (1.226 +/- 0.032), (1.182 +/- 0.082) h; AUC0-infinity were (42.168 +/- 4.007), (26.881 +/- 1.625) mg x L(-1) x h. After the cerebral ischemia-reperfusion, the activity of SOD decreased and the activity of LDH increased. Danshensu could inhibit the decrease in the SOD activity and the increase in the LDH activity within a certain period of time. This indicated that Danshensu could stay longer in cerebral ischemia-reperfusion rats than in normal rats and eliminated more slowly, which reflected the rationality of Danshensu in the clinical treatment of cerebral ischemia diseases. Danshensu's effect against the cerebral ischemic injury may be related with its level in vivo. Its plasma concentration is positively related to the SOD activity and negatively related to the LDH activity.
Animals
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Brain Ischemia
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drug therapy
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Drugs, Chinese Herbal
;
pharmacokinetics
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pharmacology
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therapeutic use
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Male
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Rats
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Rats, Sprague-Dawley
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Salvia miltiorrhiza
;
chemistry
8.Protection effect of Yindan Xinnaotong capsule and main compositions compatibility on myocardial ischemia/reperfusion injury.
Wan-Dan WANG ; Lan WANG ; Long CHENG ; Xiao-Jie YIN ; Hai-Yu XU ; Jian-Lu WANG ; Ri-Xin LIANG ; Hong-Jun YANG
China Journal of Chinese Materia Medica 2014;39(9):1690-1694
OBJECTIVETo study the protected effect of Yindan Xinnaotong capsule (YDXNTC) and main components compatibility on myocardium ischemia/reperfusion injury.
METHODGlobal ischemia/reperfusion was adopted to induce myocardial ischemia/reperfusion injury (MIRI) in isolated rat heart. Sprague-Dawley (SD) rats were divided into control, model, YDXNTC, Ginkgo biloba extract (GBE) group, ethanol extract of Salvia miltiorrhiza (SM-E) group, aqueous extract of Salvia miltiorrhiza (SM-H) group, mixed compatibility of other components in YDXNTC (MC), GBE and SM-E compatibility (GSEC), GBE and SM-H compatibility (GSHC), and SM-E and SM-H compatibility (SEHC). During the experiment, electrocardiogram was recorded to observe cardiac arrest time, heart resuscitation time, regaining normal rhythm time, the incidence and duration of arrhythmias (VT/VF). At the end of reperfusion, hearts were arrested and homogenated to assay the activity of superoxide dismutase (SOD), and the content of malondialdehyde (MDA), lactate dehydrogenase (LDH), creatine kinase-MB (CK-MB), cardiac troponin I.
RESULT(1) YDXNTC, SM-E, SM-H and MC elevated cardiac arrest time, also reduced rebeating time, restoring normal rhythm time as well as the duration of arrhythmia, but no remarkable impact on VT/VF occurrence. GBE was effective for incidence of VT/VF, also achieved good effect on shortening rebeating time, restoring normal rhythm time and arrhythmia duration. Likewise, obviously reduced rebeating time, restoring normal rhythm time and arrhythmia duration, and evaluated cardiac arrest time were also exhibited in compatibility groups except that no lengthened cardiac arrest time was detected in GSHC. And the incidence of VT/VF was decreased by GSEC. (2) YDXNT, ginkgo biloba extract (GBE), ethanol extract of salvia miltiorrhiza (SM-E), GBE and SM-E compatibility (GSEC), and SM-E and aqueous extract of salvia miltiorrhiza (SM-H) compatibility (SEHC) could improved SOD and decreased MDA level SM-H, mixed compatibility of other elements in YDXNTC (MC) and GBE and SM-H compatibility (GSHC) showed a role on MDA reduction. (3) LDH was declined by YDXNT and SM-H. CK-MB was reduced by GBE, SM-E, SM-H, and GSEC. (4) The release of cTnI was only inhibited by GSEC.
CONCLUSIONYDXNTC, primary materials and main components compatibility has a certain protection effect on MIRI, its mechanism may be related to antioxidant and calcium overload reduction.
Animals ; Arrhythmias, Cardiac ; physiopathology ; prevention & control ; Capsules ; Creatine Kinase, MB Form ; metabolism ; Drugs, Chinese Herbal ; pharmacology ; Electrocardiography ; Ginkgo biloba ; chemistry ; Heart ; drug effects ; physiopathology ; In Vitro Techniques ; L-Lactate Dehydrogenase ; metabolism ; Male ; Malondialdehyde ; metabolism ; Myocardial Reperfusion Injury ; metabolism ; physiopathology ; prevention & control ; Myocardium ; metabolism ; pathology ; Phytotherapy ; Plant Extracts ; pharmacology ; Protective Agents ; pharmacology ; Rats ; Rats, Sprague-Dawley ; Salvia miltiorrhiza ; chemistry ; Superoxide Dismutase ; metabolism ; Troponin I ; metabolism
9.Electrophysiological characterization of long QT syndrome associated mutations V630A and N633S.
Hai-ru SHE ; Si-yong TENG ; Jie-lin PU ; Zheng-lu SHANG ; Ru-tai HUI
Chinese Journal of Cardiology 2006;34(6):523-527
OBJECTIVETo identify the electrophysiological properties of long-QT syndrome (LQTS) associated missense mutations in the outer mouth of the HERG potassium channel in vitro.
METHODSMutations V630A and N633S were constructed by Megaprimer PCR method and cRNA were produced by T7 RNA polymerase. The electrophysiological properties of the mutation were investigated in the Xenopus oocyte heterologous expression system.
RESULTSCoexpression of mutant and wild-type HERG subunits caused a dominant-negative effect, and the currents were significantly decreased. Compared with wild-type HERG channels, V630A and N633S mutations were related to decreased time constants for inactivation for V630A/WT and N633S/WT at all potentials, reduced slope conductance and the voltage dependence of steady-state inactivation was shifted to negative potentials for V630A/WT and N633S/WT.
CONCLUSIONPresent study shows that LQTS associated missense mutations located in the outer mouth of HERG cause a dominant-negative effect and alterations in steady-state voltage dependence of channel gating of heteromultimeric channels suggesting a reduction in expressional current might be one of the pathophysiologic mechanisms of LQTS.
Animals ; DNA Mutational Analysis ; ERG1 Potassium Channel ; Electrocardiography ; Ether-A-Go-Go Potassium Channels ; genetics ; Humans ; Long QT Syndrome ; genetics ; Mutation, Missense ; Oocytes ; Patch-Clamp Techniques ; RNA, Complementary ; Xenopus
10.Effect of Yinghua Pinggan granule against influenza A/H1N1 virus in vivo.
Xue-qian PENG ; Yu HE ; Hui-fen ZHOU ; Yu-yan ZHANG ; Jie-hong YANG ; Jun-kui CHEN ; Yi-yu LU ; Hai-tong WAN
China Journal of Chinese Materia Medica 2015;40(19):3845-3850
To study the effect of Yinghua Pinggan granule (YHPG) against influenza A/H1N1 virus in vivo and on the immunologic function of infected mice. The intranasal influenza virus infection was adopted in ICR mouse to establish the influenza virus pneumonia model. At the 3rd and 7th day after the infection, the lung index and pathologic changes in lung tissues of mice were detected. Realtime PCR and flow cytometry were employed to observe the virus load in lung tissues and the levels of CD4+, CD8+, and CD4+/CD8+ in peripheral blood. The result showed that at the 3rd and 7th day after the infection, YHPG (15, 30 g x kg(-1)) can significant decrease in the lung index and virus load in lung tissues of mice infected with influenza virus, alleviate the pathologic changes in lung tissues, significantly increase the levels of CD4+ and CD4+/CD8+ ratio and reduce the levels of CD8+ in whole blood. This indicated that YHPG can inhibit the influenza virus replication, alleviate pulmonary damage and adjust the weak immunologic function of infected mice, with a certain therapeutic effect on mice infected by H1N1 virus in vivo.
Animals
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Antiviral Agents
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administration & dosage
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Humans
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Influenza A Virus, H1N1 Subtype
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drug effects
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genetics
;
physiology
;
Influenza, Human
;
drug therapy
;
pathology
;
virology
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Lung
;
pathology
;
virology
;
Male
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Mice
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Mice, Inbred ICR
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Virus Replication
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drug effects