The contentofthe pharmacology is huge and full of variety of drugs,therefore,easy to confuse,besides,it's difficult to understand the abstract mechanism.This article describes the pharmacology teaching methods such as disease example,comparison,practice and so on.These methods stimulate students'interest in studying and learning initiative as well as train students'abilities to discover,analyze and solce problems,and at last have achieved good teaching effects.

60 mm Hg (PP1 group) or 40 mm Hg≤PP≤60 mm Hg (PP2 group),1 mm Hg =0.133 kPa.Ambulatory blood pressure monitoring,the serum and urine ?_2-MG,urine mAlb,blood BUN and Cr were measured in both groups,the blood pressure,serum and urine ?_2-MG,urine mAlb,blood BUN and Cr were compared between two groups. Results Compared with PP2 group,the PP1 group showed higher levels of renal function indexes. Conclusion Renal damage is related with pulse pressure in senile essential hypertension.

An isocratic high-performance liquid-chromatographic method is-described for the simultaneously determining carbamazepine and its biologically active metabolite, carbamazepine-10, 11-epoxide. Serum samples containing an internal standard (10-methoxycarba-mazepine) are extracted with dichlor-methane and 4 mol ? L-1 sodium hydroxide. The organic extract are evaporated at ambient temperature under a stream of nitrogen. The residues are reconstituted in mobile phase and injected on to a re-versed-phase C18 Column (150?4. 6mm I. D). The mobile phase consists of ace-tontrile/methanol/water (50/210/260 by vol) . The UV detector is operated at 214nm. The elution times of all com-pounds are within 7 min.The least detectable concentrations of carbamazepine and carbamazepine-10, 11-epoxide are 0. 08mg ? L-1 and 0.1mg ? L-1, respectively. The average absolute recovery for carbamazepine is 96.0% and for carbamazepine-10,11-epoxide is 97.3%. Within-run CV is 3. 3%~5.7%. and between-run CV is 4.3%~9.0%. The standard curve is linear at least within 40mg ? L-1 for carbamazepine and within 20mg ? L-1 for carbamazepine-10, 11-epoxide.

Objective To investigate the rule of the aquaporin 4 (AQP 4) expression in the acute ischemic cerebral tissues, and to study the molecular biologic mechanism of diffusion weighted imaging (DWI). Methods Thirty six Wistar rats were divided into 2 groups randomly, including control group ( n = 12) and operation group ( n =24). The operation group was studied after the right middle cerebral artery was unilaterally occluded (MCAO) at an interval of 15 min, 30 min, 1 h, 3 h, 6 h, and 24 h, respectively ( n =4 for each sub group). The operation process of the control group was the same as the operation group except MCAO. All rats in both groups were examined with DWI. The relative ADC (rADC), relative density (rd), and relative area (rs) of the biggest hyperintensity signal layer on DWI were measured. After that, the animals were sacrificed and perfused with the mixture solution consisting of TTC at different time intervals. The biggest layer of the ischemic cerebral tissues stained with TTC and corresponding to that of DWI was examined with immunochemistry and in situ hybridization. The AQP 4 expression AQP 4 (△S and ?) was measured with the Image Analyzer. Meanwhile, histologic examination was performed at each group. Results There was no significant change of the DWI and the pathology, as well as the AQP 4 expression in the control group. In the operation group, abnormal high intensity was found in DWI of ipsilateral MCA territory at 15 min after MCAO, and rADC value decreased quickly within 1 h after MCAO, while the AQP 4 expression, the rd DWI, and the rs DWI increased rapidly in the stage. With the progress of the time, the rADC value further decreased at 3 h, and then began increasing slowly till 24 h . But the AQP 4 expression (△S and ?) and the rd as well as the rs continuously increased slowly between 1 h and 6 h after MCAO, then they had an increasing peak except the rd. The AQP 4 expression, rd DWI, and rs DWI all showed positive linear relationship with time, presenting as 2 peaks and a plateau. The corresponding sequential pathologic changes were gradual increase of intracellular edema (

Objective To investigate the clinical diagnosis and treatment of incomplete Beh et′s disease. Methods The clinical data of 52 patients (83 eyes ) with incomplete Beh et′s disease were retrospectively analysed. Visual acuity and results of examination of slit-lamp microscope, ocular fundus, and fundus fluorescein angiography (FFA) were observed and analysed. All of patients were treated by local cycloplegic, systemic treatment with glucocorticoid and cytoxan. The followed-up period was 1 year or more. Results Recurrent hypopyon or empyema of anterior chamber angle, and hyperaemia of optic papilla was found in 54 and 41 eyes, respectively. The results of FFA showed that abnormal changes were found in all of the eyes. There was vascular leakage and staining of optic papilla at the early and late stage in 83 eyes (100%), diffuse leakage of retinal capillary vessel in 83 eyes (100%), and leakage of affected branch of retinal vessel and staining of the vascular wall at the late stage in 71 eyes (85.54%).After the treatment, the disease recovered completely in 20 patients (26 eyes), recovered partly in 20 (33 eyes), and alleviated in 12 (24 eyes). No patients suffered from hypopyon or empyema of anterior chamber angle and hyperemia of optic papilla. None of the patients had oral ulcer, genital ulcer or arthritis until the last day of the follow-up. Conclusions Recurrent hypopyon, papillitis, and retinal vasculitis were the main clinical manifestations of incomplete Beh et′s disease. FFA redounds to the diagnosis of the disease and timely application of cycloplegic and systemic application of glucocorticoid and cytoxan may inhibit the aggravation of the disease effectively.

Objective This study was designed to investigate the correlation between the apparent diffusion coefficient(ADC)value and pathological change of the non-injured side brain tissue of traumatic brain injury(TBI)of rat.Methods Sixty healthy adult Wist-ar rats were randomly divided into two groups:the control or TBI groups.The TBI group was divided into five sub-groups according to the different time intervals:1,3,6,12,24 h(n = 10).The animal brain of each group was scanned with MR-DWI,and the ADC value of damaged areas and contralateral non-damaged areas were measured.After that the brains were taken out at different time points after TBI.The cerebral edema and blood-brain barrier(BBB)changes in structure were examined with an optical micros-copy and transmission electron microscopy,and the IgG content in the same tissues were determined by means of immunohistochem-istry.The data was analyzed with SPSS 13.0 statistical software.Results There was no signal abnormality on MR-DWI and tissue structure in control group,and the IgG stain was negative.In the contralateral non-damaged areas of TBI group,pathological obser-vation revealed no variation at 1 h after TBI,and the IgG stain was also negative.Cellular edema was shown at 3 h and the IgG stain was slight positive.The cellular edema aggravated with time and angioedema appeared at 6 h.IgG stain was shown significantly posi-tive.At 12~24 h,cellular edema kept increasing more severe,however angioedema had a trend to mitigated along with time,IgG stain became slight and the proliferation of glial cells could observed.Compared with control group,the ADC values of the contralat-eral non-damaged areas in each group showed no significant difference (P >0.05).However,in the damaged areas of each group, angioedema appeared at 1 h and gradually aggravated,cellular edema occurred at 3 h,Both of them were aggravated with time. ADC values increased at 1 h,and then decreased until 6 h,then followed a climbing up to 24 h,showed as a “V”-shaped.Con-clusion When contused on one side brain,the contralateral non-inj ured side tissue also has pathological changes that occurs later than those on the inj ured side.Cellular edema of the tissues ap-peares first and is followed by angioedema,which lessens over time..There is no significant difference of ADC values between con-tralateral side of TBI groups and control group(P >0.05),which reveals a “pseudo-normal”phenomenon.

BACKGROUND: Methyl cobalamin, a derivative of vitamin B12, .can promote the metabolism of nucleic acid protein, axoplasmic transport and axonal regeneration.OBJECTIVE: To observe the role of target muscular injection of methyl cobalamin ofdifferent dosages in the regeneration of peripheral nerve injury in rats.DESIGN: A randomized and controlled animal experiment.SETTING: Changzhou Second People's Hospital affiliated to Nanjing Medical University.MATERIALS: The experiment was carried out in March 2003. Thirty healthy Wistar rats were randomly divided into three groups with 10 rats in each group: high-dosage group, low-dosage group and blank control group.METHODS: All the rats were made into models of sciatic nerve injury by epineural suture immediately after transection of left sciatic nerve. Rats in high- and low- dosage groups were injected with methyl cobalamin of 300and 100 μg/kg per day respectively, and those in blank control group were injected with 1 mL normal saline of the same volume, and target muscular injection was given once a day postoperatively. At postoperative 4 and 8weeks, 5 rats were killed at one time; the wet mass of left triceps surae muscle was measured. Morphological observation of sciatic nerve under light and electron microscopes and imaging analysis were made as the detected indexes to analyze the effect of methyl cobalamin of different dosages on sciatic nerve injury in rats.sciatic nerve myelin sheath at postoperative week 8.parison of the wet mass of triceps surae muscle at postoperative 4 weeks: It was higher in high-dosage group than in low-dosage group and blank control group [(1.367±0.012) g, (1.164±0.011) g, (0.950±0.009) g, P ＜ 0.05].week 8: It washigher in high-dosage group than in low-dosage group and blank control group [(2.205±0.015), (1.611±0.013), (1.230±0.014) g, P ＜ 0.05].weeks postoperatively: It was obviously higher in high-dosage group than in low-dosage group and blank control group [(13.30±1.167), (9.453±1.233),atic nerve myelin sheath at 8 weeks postoperatively: It was thicker in highdosage group than in low-dosage group and blank control group [(1.145±0.108),(0.806±0.065), (0.560±0.045) mm, P ＜ 0.05].CONCLUSION: Target muscular injection of methyl cobalamin can promote the regeneration of peripheral nerve, and methyl cobalamin of high dosage can better play its role in nourishing injured nerve.

Objective:To evaluate MRI manifesattions of intradural metastases of medulloblastomas.Methods:The clinical data and MRI of 6 cases with intradural metastasis of medulloblastomas were reviewed retrospectively.Results:21 masses were found in 6 cases,mostly in lumbar segment.Most of them were oblong or fusiform shagped.The size averaged 1.8 cm?2.3 cm.They had the similar signal intensity with those in brain,but hemorrhage,cyst and calcification were less common.Conclusion:MRI plays an importment role in diagnosis of intradural metastases of medulloblastomas. [

Further study of the effect of monosodium glutamate on body temperature using rabbits as experimental model by repeatedly intravenous injection of MSG. The experimental results showed that the body temperature of rabbits were decreased significantly at a time of each day consecutively for three days with medium dose MSG(0.5g/kg/day) However, this effect was disappeared following the fourth administration of MSG a week later, and so did the fifth administration of MSG two weeks later. Those results suggested that the disappearance of decreased body temperature by MSG may be due to tolerance development after MSG was administrated repeatedly. The authors proposed two hypotheses of mechanisms for the development of MSG"tolerance". which would be investigated further.

The pollution levels were slight-pollution for most of unqualified cosmetics.The results of health risk assessment showed that all of the cosmetics were security.Conclusion On the whole,the qualities of cosmetics that are used in beauty and hairdressing salon are qualified,but they still don’t match the new standard well,and there are still a few of cosmetics unqualified.