1.The influence of edaravone on serum IL-6、 TNF-α、 ET、 sICAM-1 and MCP-1 in acute intracerebral hemorrhage patients
Chinese Journal of Primary Medicine and Pharmacy 2012;19(15):2250-2251
Objective To study the influence of edaravone on serum IL-6,TNF-α,ET,sICAM-1 and MCP-1 in acute cerebral hemorrhage patients,discuss the protective mechanism of edaravone on cerebral hemorrhage.Methods 100 patients with acute cerebral hemorrhage were randomly divided into treatment group and control group (50 cases),the serum levels of IL-6,TNF-α,ET,sICAM-1 and MCP-1 were detcted by ELSA at pretherapy and after given treatment.Neurological functional deficit scores were utilized for assessment at pretherapy and after given treatment.A healthy control group which approximately matched the experimental group included 30 persons.Results The levels of serum IL-6,TNF-α,ET,sICAM-1 and MCP-1 in both two groups after treatment were significantly lower than those before treatment( all P < 0.05 ),and the levels of serum IL-6,TNF-α,ET,sICAM-1 and MCP-1 in edaravone therapy group significantly lower those that in conventional therapy group( P <0.05 ).NDS of both groups after treatment were lower than those before treatment (P < 0.05 ),and the scores of edaravone therapy group were significantly lower than those of conventional therapy group( P < 0.05 ).Conclusion Edaravone can decrease the levels of IL-6,TNF-α,ET,sICAM-1 and MCP-1 in patients with acute cerebral hemorrhage.It could lighten acute inflammation and brain injured,lessen nerve function impairment,and protect the tissue of brain.
2.Tumor Inhibition of Acid-Responsive Polymer-Cisplatin Conjugate Nanoparticles Drug Delivery System
Herald of Medicine 2014;(9):1132-1136
Objective To synthesize polymer-cisplatin conjugate nanoparticles for acid-responsive drug delivery, and verify the inhibitory effect of the nano-system on cancer cells. Methods Acid-responsive polymer-cisplatin conjugate nano-drug carrier was synthesized to simulate the drug release under an acidic environment. Cell viability was examined by MTT assay. Results The polymer-cisplatin nanoparticles exhibited well-controlled cisplatin loading rate, and excellent acid-responsive drug release kinetics. At pH 7. 4, little drug was released. At pH 5. 0 or 6. 0,the drug release was significant. Compared with free cisplatin,cisplatin in the conjugate nanoparticles showed higher cytotoxicity against ovarian cancer cells in vitro. An equivalent dose of 7 μmol·L-1 cisplatin loaded in the conjugate nanoparticles exhibited same cytotoxicity as 50μmol·L-1 free cisplatin.Conclusion Polymer-cisplatin conjugate is an acid-responsive drug delivery system that greatly improves the bioavailability of cisplatin to tumor cells. It is expected to play a better tumor inhibition effect by quickly releasing a high dose of chemotherapy drug inside tumor cells.
3.Diabetes mellitus and primary liver cancer: risk factor or real cause?
Journal of Clinical Hepatology 2017;33(4):757-762
With an increasing prevalence all over the world,diabetes mellitus is considered as a potential cause of liver cancer in patients with non-viral hepatitis.Whether diabetes mellitus is the cause of liver cancer and related pathogenesis remain unknown.The article reviews recent large-sample cohort studies and confirms that diabetes mellitus increases the incidence rate of liver cancer and affects its prognosis.This article also investigates the association of hepatitis C,obesity,and nonalcoholic fatty liver disease with diabetes mellitus and liver cancer and finds that insulin resistance and activation of chronic inflammatory factors may be involved in the generation and proliferation of cancer cells.This article elaborates on the influence of anti-insulin resistance drugs on the development and progression of liver cancer and points out that diabetes mellitus may be the cause of liver cancer.Effective control of insulin resistance can help to reduce the development and progression of diabetes-associated liver cancer.
4.EFFECTS OF NATIVE ISOSORBIDE MONONITRATE ON HEMODYNAMICS IN RATS WITH MYOCARDIAL INFRACTION
Chinese Pharmacological Bulletin 1987;0(02):-
Tho effects of native isosorbide mononitrate ( ISMN ) on the hemodynamics in rats with early myocardial infarction by left coronary artery occlusion were investigated. LVSP and dP/dtMAX were increased, and LVEDP was decreased with ISMN 5mg/kg i.v. 20 min after coronary occlusion. However, ISMN did not significantly effect the HR, SAP, DAP and MAP. The results showed that ISMN can improve cardial function in early myocardial infarction.
5.Sites of action of propofol and isoflurane on somatosensory pathway
Chinese Journal of Anesthesiology 1994;0(03):-
Objective To determine the sites of action of propofol and isoflurane on somatosensory pathway using median nerve somatosensory evoked potential(MnSSEP) .Methods Twenty-six ASA I - II patients aged 20-50 yrs were randomly divided into two groups: I propofol group( n = 13) and H isoflurane group( n = 13) .In propofol group patients received propofol infusion at a rate of 10 mg?kg-1?h-1 .Oxygen was administered via mask and respiration was assisted or controlled to maintain SpO2 at 96%-100% and PETCO2 at 35-45 mm Hg. The propofol infusion was continued until the patient failed to respond to verbal command. Six minutes later if the patient was still breathing spontaneously, the rate of propofol infusion was increased to 20-40 mg?kg-1?h-1 . In isoflurane group anesthesia was induced with propofol 2 mg ? kg-1 and intubation was facilitated by succinylcholine and anesthesia was maintained with isoflurane inhalation and intermittent iv boluses of vecuronium. The end-tidal isoflurane concentration was maintained at 0.5,1.0 and 1.5 MAC. Each concentration was maintained for 15 minutes. MAP, HR, SpO2,PCTCO2, T0(naso-pharyngeal) and BIS were continuously monitored. MnSSEP( Viking IV D type) was measured and recorded before induction of anesthesia(baseline) and in propofol group when patients became unconscious and apneic; in isoflurane group when end-tidal isoflurane reached 0.5,1.0 and 1.5 MAC.Results In group I there was no change in both latencies and amplitudes of N9 and N13'.With increasing infusion rate, propofol gradually prolonged the latencies and decreased the amplitudes of N60, P45, N35, N20 and P25 waves. In isoflurane group there was no change in the latencies and amplitudes of N9. There was no change in the latencies of N13', but the amplitudes decreased at 1.0 and 1.5 MAC. With increasing concentration, isoflurane gradually prolonged the latencies and decreased the amplitudes of P45, N60, N35, N20 and P25 waves. At 1.5 MAC the inter-peak latencies between N13'-N20 and N13'-P25 were prolonged. Conclusions The sites of action of different infusion rates of propofol and different concentrations of isoflurane are different on somatosensory pathway. The higher the doses, more widespread are the sites of action.
6.Application of Manual Stitching Technique for Digital Radiography in Total Knee Arthroplasty
Acta Medicinae Universitatis Scientiae et Technologiae Huazhong 2014;(4):456-458,459
Objective To obtain panorama X-ray images of the lower extremity with a simple method,eliminate the mosai-cing error,and apply this manual stitching technique for digital radiography to the measurement of the force line in total knee arthroplasty.Methods The track of X-ray tube was preset,and Dicom format data were collected by using digital X-ray ima-ging.Then,the data were imported to photoshop CS4 for manual image registration and image fusion.The reliability of the film was tested by comparing the vertical length of the body symbols proj ection in the coronal plane with that on the panorama X-ray (AutoCAD 2010)images.Moreover,the hip-knee-ankle angle was compared before and after operation.Results The matching sample t-test showed there were no significant differences in the length(4 groups of data)between the greater trochanter femur and the fibular head,and between the fibular head and the lateral malleolus between before and after operation(P>0.05 for all) .The hip-knee-ankles angle was much greater after operation than that before operation.Conclusion This manual stitching technique for digital radiography can produce seamless and precise panorama X-ray images,which can be used to reflect the length and angle of the lower extremity before and after operation.
7.The relationship of gap junction with the bystander effect in the HSV-TK/GCV treatment
Chinese Pharmacological Bulletin 1987;0(01):-
The bystander effect(BE) plays an important role in the gene therapy of cancer by the herpes thymidine kinase/ganciclovir(HSV-TK/GCV) system.It enhances the therapeutic efficacy of this system.Up to now,the exact underlying mechanism of the bystander effect remains unclear.A large body of evidence has indicated a close correlation of the connexin expression and gap junction in the targeted cells to the bystander effect.Here the publications concerning the relationship of gap junction with the bystander effect in the HSV-TK/GCV treatment have been reviewed.The possible cell death signals that can be transferred through gap junction to induce the bystander effect are also discussed.
8.Analysis of Labeled Items in Package Inserts of 51 Kinds of Ointment for External Use
China Pharmacy 2017;28(16):2286-2288
OBJECTIVE:To provide reference for reasonably designing package inserts of ointment for manufacturers. METH-ODS:According to items included in Management Regulation for Package Insert and Label and Specification for Chemicals and Bi-ological Products for Treatment,labeled items in package inserts of 51 kinds of ointment for external use during Jan.-Jun. 2016 in our hospital were analyzed. RESULTS:Among the 51 kinds of ointment,39 were domestic varieties and 12 were imported variet-ies. In the package inserts of 39 domestic varieties,items with lower labeling rates were overdose,pharmacokinetics,use guid-ance,pharmacology and toxicology,with labeling rates of 2.6%,5.1%,15.4%,28.2%;while the labeling rates of imported vari-eties were 16.7%,83.3%,75.0%,100%. Compared with package inserts of imported ointment,composition,dosage and usage, adverse reactions,contraindications,precautions,drug interactions,medication for special populations were not enough detailed in domestic ointments. CONCLUSIONS:It is suggested that manufacturers consult medicine experts, list all auxiliary materials through Management Regulation for Drug Description and Label,refine and improve the labeling contents of dosage and usage,ad-verse reactions,precautions,medication for special populations,pharmacology and toxicology,overdose,etc. In addition,admin-istrative departments should strengthen the regulatory approval efforts.
9.Immunohistochemical study of dehydroepiandrosterone in rat gastric epithelial cells
Tao LIANG ; Taihui FANG ; Wei LIANG
Journal of Medical Postgraduates 2001;14(2):115-116
Objectives:To study the localization of dehydroepiandrosferone (DHEA) in rat gastric epithelial cells.Methods:The immunohistochemical SABC was used.Results:The parietal cells in gastric epithelial cells appeared DHEA positive immune reaction.The positive substance was distributed in the cytoplasm and negative in the nuclei.Conclusions:Parietal cells had DHEA,which might play an important role in the regulation of digestive function.
10.Influence of Recombinant Human Growth Hormone Replacement Therapy on Glucose Metabolism in Children with Growth Hormone Deficiency
Journal of Applied Clinical Pediatrics 1992;0(06):-
Objective To evaluate the effects of recombinant human growth hormone(r- hGH)replacement therapy on glucose metabolism in children with growth hormone deficiency(GHD) Methods Replacement therapy with domestic r - hGH was done in 15 children with GHD for 3 months. Oral glucose tolerance test (OGTT) and insulin .releasing test (IRT) were performed before and after 3 months of r-hGH replacement therapy. Venous blood was sampled before and 30,60,120 min after glucose load for measurements of plasma glucose (PG) and insulin (INS).Results OGTT were normal in 15 patients before treatment. After 3 months of r-hGH therapy, fasting plasma glucose remained unchanged, but PG 30 min(P