Fifty-two adult male rabbits, weighing 2～3kg, were divided into three groups. 1. Peptic ulcer were induced in 25 animals by injecting 0.3ml/kg of 40％ acetic acid into the submucosa of the stomach after laparotomy under aseptic conditions 2. 19 animals were operated as above but the same amount of normal saline were injcted instead of acetic acid 3. 8 normal rabbits were raised under the same conditions without any treatment and served as controls. The thyroid glands of three groups were taken at definite time intervals (1～40 days) after the operation. The right thyroids were prepared for cryostat sections after hexane quenching (-60℃) and subjected to enzyme histochemical studies. The left thyroids were fixed in Carnoy's fluid and subjected to histological and other histochemical studies. The following results were observed.The reactions of enzymes of follicular cells were weaker than the normal in the animals of the second group during the period of 3～21 days after the operation and injection of saline. The follicular ceils became flattened and follicular lumens increased in size. These changes began to show signs of recovery on the 28th day of the experiment. In the follicular cells of the first group of animals in which peptic ulcer developed after injection of acetic acid, the similar changes were observed as in the second groug of animals during the early period of 1～3 days after operation, but from 7 to 21 days after the operation, the reactions of Acid phosphatase, Succinate dehydrogenase, Glucose-6-phosphate dehydrogenase, Glycerphosphate dehydrogenase, Peroxidase, Adensine triphosphatase and Alkaline phosphatase were stronger and the sizes of follicular lumens were smaller, the colloid droplets were more numerous than those of the animals of the second group. These changes in the follicular cells of animals of the first group began to show signs of recovering toward norrnal on the 28 th day and became almost normal on the 40 th day after operation.These findings suggest that the thyroid follicular ceils were involved in the regulatory activities of the organism for the healing of the peptic ulcer.

The histological and histochemical changes in the C cells of the rabbit thyroid during experimental peptic ulcer were studied. Acetylcholinesterase was used as the marker enzyme to identify C cells. Forty-nine adult male rabbits were randomly divided into three groups: 1. In the experimental peptic ulcer group, 24 animals were induced to develop peptic ulcer by injecting 0.15 ml/kg of 40% acetic acid into the submucosa of the stomach after laparotomy under aseptic conditions. 2. In the saline control group, 18 animals were injected with 0.15ml/kg of normal saline into the submucosa of the stomach after laparotomy. 3. In the normal control group, 7 rabbits were raised under the same conditions as groups 1 and 2 without any treatment. Thyroid glands were removed at different time intervals (1-28 days) after the operation. The right thyroids were prepared for cryostat sections and subjected to enzyme histochemical studies. The left thyroids were fixed in Carnoy's fluid and subjected to histological and other histochemical studies. The findings were as follows.In the C cells from the normal control group, the reactions of acetylcholinesterase, nonspecific esterase and acid phosphatase were rather strong. Acetylcholinesterase can be taken as a specific marker enzyme for C cells. The reactions of thiamine pyrophosphatase, succinate dehydrogenase, lactate dehydrogenase, glucose-6-phosphate dehydrogenase and ribonucleic acid were weak which suggested that normal C cells were a at a lower state of functional activity. In the saline control group, the histochemical changes showed that the C ceils were in an active functional state during the early period of the experiment, which may possibly reflect the response of C cells to the operation stress and wound healing. In the experimental peptic ulcer group, the reactions of acetycholinesterase, nonspecific esterase, acid phosphatase, succinate dehydrogenase, glucose-6-phosphate dehydrogenase, thiamine pyrophosphatase and ribonuclic acid of the C cells in the experimental peptic ulcer group were stronger than those of the saline control group 7-28 days after the operation. These histochemical changes of C cells duting this period may suggest that the C cells were active in function and perhaps participated in the regulatory activities of the organism during its recovery from the disease. In none of the three groups did the C cells show any conspicuous histological and morphological changes at any time in the experiment.

Eighty adult male Wistar rats were randomly divided into three groups: 1. In the experimental peptic ulcer group, 35 animals were induced to develop peptic ulcer by injecting 0.05 ml/kg of glacial acetic acid (more than 99%) into the submucosa of the stomach after laparotomy under aseptic conditions. 2.In the saline control group, 35 animals were injected with 0.05 ml/kg of saline into the submucosa of the stomach after laparotomy. 3.In the normal control group, 10 normal animals without any treatment were raised under the same condition as group 1 and group 2. The thyroid glands of three groups were taken at definite time intervals (1-28 days) after the operation. The right thyroids were prepared for cryostat sections after hexane quenching (-60℃) and subjected to the histochemical studies of acid phosphatase (AcP), alkaline phosphatase(AIP), a-glycerophosphate dehydrogenase (a-GPD), succinate dehydrogenase (SDH), glucose-6-phosphate dehydrogenase (G6PD), and nonspecific esterase (NsE). The left thyroids were fixed in Carnoy's fluid, stained with HE and subjected to histological study. The reactions of enzymes of the follicular cells in the group 2 were weaker than those in the group 3 (normal control) during the period of 2-21 days after the operation. The follicular cells became flattened and follicular lumens increased in size. These changes recovered to normal on the 28th day after the operation. In the follicular cells of group 1. In which peptic ulcer developed after injection of glacial acetic acid, the reaction of A1P was weaker than those in the group 3, but stronger than those in the group 2. The reations of a-GPD, SDH, and G6PD were stronger than those in the group 2, and as well as those in group 3. The reaction of AcP was stronger than those in the group 2 and group 3 during the 6-21 days after the operation. The follicular cells in the group 1 became flattened and the follicular lumens increased in size only during the period of 4-10 days after the operation and recovered on the 14th day after the operation. These findings suggested that the thyroid follicular cells of rat involved in the metabolic activities of the repair of gastric ulcer.

Using a quantitative method, the healing of the experimental gastric ulcer in rats was studied in various states of thyroid function. Rats were made hypothyroid by ingestion of thiouracil (0.1％ solution in drinking water for 10 days). Rats were made slightly hyperthyroid by ingestion of thiouracil and simultaneous administration of T_4 (3?g/100 g/day,ip) for 10 days. Rats were made hyperthyroid by administration of excess T_4 (10?g/100 g/day, ip) for 10 days. The normal rats served as controls. In all of these rats, gastric ulcer was induced by injecting a small quantity of glacial acetic acid into the submucosa of the stomach after laparotomy under aseptic conditions. After operation the rats in four groups were given those drugs as above respectively for 10 days. The volume (7.71?0.52mm~3' 5.5?0.78 mm~3 for control) and area (8.29?0.90mm~2; 4.39?0.73mm~2 for control) of gastric ulcer increased in the rats with hypothyroidism. The healing rate of gastric ulcer retarded (-30?9.4％ for volume healing rate, -50?2.1％ for area healing rate). The volume (4.75?0.88mm~3) and area (4.05?0.93mm~2) of gastric ulcer decreased in the rats with slight hyperthyroidism, and the healing rate of gastric ulcer accelerated (37?3.8％ for volume healing rate, 49?3.2％ for area healing rate). The volume (4.88?0.90mm~3) and area (6.16?0.74mm~2) and the healing rates of gastric ulcer in the rats with hyperthyroidism were similar as those of control. These findings suggested that (1) thyroxine is necessary for healing of the experimental gastric ulcer in rats and (2) thyroxine seem to accelerate healing of the experimental gastric ulcer in rats.

Objective To evaluate the application of optical coherence tomography (OCT) in the rat retinal light damage. Methods Albino Sprague-Dawley (SD) rats (5-8 weeks of age) were exposed to 1 000-1 400 lux of diffuse, cool, white, fluorescent light for 2, 5, and 7 d. OCT image analysis and histological measurements of the retinal thickness were performed. Animals were then sacrificed and the measured results were compared with those by histological examination. Results The sensory retinal thickness of the retina in the rats thinned progressively as the retinal degeneration was in progress. The sensory retinal thickness measured by OCT [the corresponding thickness was (179.11?12.01)?m, (159.27?12.81)?m, and (133.67?11.43)?m, respectively] was well correlated with that measured by histology [the sensory retinal thickness after exposure to the light for 2, 5, and 7 d was (144.26?9.36)?m, (116.16?11.24)?m, and (94.27?10.68)?m, respectively] (r= 0.995, P

Objective To investigate the morphological features of choroidal neovascularization (CNV) in central exudative chorioretinopathy (CEC) using optical coherence tomography (OCT). Methods OCT and fundus fluorescein angiography (FFA) were performed in 41 cases (43 eyes) of CEC,and the course of CEC disease was from 1 week to 10 months. Twenty seven of 43 eyes were also examined by indocyanine green angiography (ICGA). Results OCT images revealed 5 kinds of morphological features of CEC: well defined CNV(41.86 %),poorly defined CNV(30.23 %),hemorrhagic pigment epithelium detachment (PED)(16.28 %), CNV companied with serous (6.98 %) or hemorrhagic neurosensory retina detachment (4.65 %). CNV mainly showed well defined and poorly defined CNV (72.09 %).In those eyes that could clear define the CNV boundary,there were 12 eyes on FFA examination and 20 eyes on ICGA examination which defined the boundary from retinal horizontal plane, while there were 23 eyes on OCT examination which defined the boundary from retinal vertical section. Classic CNV on FFA consistently presented with well defined boundaries on OCT ,whereas non classic CNV had a variable cross sectional appearance. Conclusions The OCT morphological features of CNV in CEC is mainly well defined CNV and poorly defined CNV; OCT examination can precisely observe the retinal and choriocapillaries pathological anatomy of CEC from retinal vertical section, in making the CEC diagnosis as an important complementary examination of FFA and ICGA which observe the focus from retinal horizontal plane.

The cells containing 5-hydroxytryptamine (5-HT) in the antrum of the SD rat's stomach were demonstrated by means of Sternberger's PAP immunohistochemical method and quantitative analysis were performed by means of Weibel's stereological method. The results were as follow: The 5-HT immunoreactive cells in the antrum of the rat's stomach were found only in the surface epithelium and the glandular epithelium of the mucosa. The volume density (V_v) was 0.0038?0.0004, the surface density (N_A) was 42.86+3.20 cells/mm~2 and the numerical density (N_v) was 2627.11?200.42 cells/mm~3. The distribution of 5-HT reactive cells showed an obvious regional difference. From the lesser curvature to the greater curvature of stomach, the cell density decreased gradually. The cell density was the highest in the lesser curvature: N_A was 59.96?3.48 cells/mm~2, Nv was 3729.23?216.89 cells/mm~3; and was second high in the two side walls: N_A was 42.39?3.48 cells/mm~2, Nv was 2647.18+216.57 cells/mm~3; and was lowest in the greater curvature: N_A was 29.39? 4.49 cells/mm~2, N_v was 1843.00?280.09 cells/mm~3. Most of the 5-HT immunoreaclive cells were found in the basal third section of the mucosa and the cell density was the highest. N_A was 92.33?6.92 cell/mm~2,N_v was 5336.28?410.22 cells/ mm~3; in the middle one third of the mucosa, the cell density came to next: N_A was 27.69?2.38 cells/mm~2, N_A was 1708.68?146.65 cells/mm~3; and in the superficial third section of the mucosa, the cell density was the lowest: N_A was 7.29?0.53 cells/mm~2, N_v was 457.00?35.44 cells/mm~3. In addition, a detailed observation on the morphology of the 5-HT immunoreactive cells was also undertaken.

Objective To observe the intervention effect of BrainHQ visual training on depressive symptom in patients with post stroke depression.Methods Eighty patients with post stroke depression were divided into control group(n=40)and intervention group(n=40).The control group accepted routine drug therapy and conventional rehabilitation, while intervention group received BrainHQ visual training additionally.They were assessed with Hamilton depression scale(HAMD) before and 4 weeks after intervention.Results Before intervention the HAMD score between control group and intervention group(respectively(19.80±3.96), (18.43±2.94)) had no statistical difference (P＞0.05).After 4-week intervention, the HAMD score of intervention group(9.58±5.42) was significantly lower than that of control group (13.85±5.73)(P＜0.01).Before the intervention, depression level of two groups had no difference(P＞0.05).After 4-week intervention,the difference of depression level was statistically significant in two groups(P＜0.05).Conclusion BrainHQ visual training can improve depressive symptom in patients with post stroke depression.

(DBI) in rats by observation on the changes of Homer 1a expression and apoptotic nerve cells . Methods Spraque-Dawlley(SD) rats were randomly ( random number ) divided into control group and severe DBI group .DBI rat model was established according to the de-scription of Marmarou′s diffused brain injury .No injury was done on control group .The changes of neuron pathology were observed by light microscopy and electron microscope .The expression of Homer1a was observed by immunohistochemistry and western blot .The quan-tity of apoptotic cells was measured by terminal deoxynucleotidyl transfernase medicated nick end labeling ( TUNEL) method. Results The death rate of rats in severe DBI group was 49.3%.Compared with the control group , the ultrastructures in hippocampal neurons in-cluding organelle , axonal and capillary were damaged seriously after injury , the survival rate of nerve cells decreased significantly at 1 h after injury ([99.4 ±0.6]%vs [94.4 ±5.6]%, P<0.05), and peaked at 72 h ([99.2 ±0.8]%vs [54.7 ±33.8]%, P<0 .05) in DBI group.The expression of Homer1a protein increased significantly at 1 h after injury(0 .136 ±0.024 )and peaked at6 h(0.178 ± 0.028) and maintained to 24 h (0.176 ±0.027), while decreased at 48 h (0.145 ±0.02)and 72 h (0.117 ±0.012) in DBI group;the expression of Homer 1a was obviously higher at each time point in DBI group than that in control group (P <0.05).The apoptoticindex of TUNEL positive cells increased at 6 h and demonstrated significant difference at 72h in comparison to control group ([41.78 ±3 .96]%vs [1.92 ±0.22]%, P<0.05).The correlation analysis indicated that Homer1a expression from 1~24 h and 24 h~72 h was related to the survival rate of nerve cells ( r=-0.726, P<0.05; r=0.842, P<0.05) and the quantity of TUNE positive cells(r=0.738, P<0.0;5 r=-0.898, P<0.05). Conclusion The dynamic expression of Homer1a in hippocampus after severe DBI can reflect nerve cell loss.

Objective To investigate the effects of inhibitors U0126 on expression of ERK1/2 and Ku70 in the hippocampus in diabetic rat after global cerebral ischemia and reperfusion.Methods The global cerebral ischemia model of diabetic rat was made by streptozotocin-induction with four-vessel occlusion of modified Pulsinelli' s method.Adult male SD rats (n =80) were randomly (random number) divided into 4 groups (n =20 rats per group),namely sham operation (SO) group,normoglycemia ischemia/reperfusion (NI/R) group,diabetes cerebral ischemia (DCI) group and DCI + U0126 (0.01 mg/kg Ⅳ)group.The morphological changes of neuronal cells were observed by using HE staining 1 h,6 h,24 h and 48 h after I/R; and immunohistochemistry method was used to detect the levels of phosphorylated ERK1/2 and Ku70 protein.Statistical analysis of experimental data was carried out by using SPSS 17.0 software.Comparisons between groups were done by using factorial variance analysis,and difference was statistically significant at P ＜ 0.05.Results Compared with SO group,some neurons showed histopathologic changes of neuronal necrosis and apoptosis in NI/R group as well as the phosphorylated ERK1/2 levels increased at 1,6,24,48 h (P ＜ 0.05) ; The Ku70 levels increased at 1,6 h (P ＜ 0.05) and were lower at 24 h,48 h (P ＜ 0.05) ; Compared with the NI/R group,the histopathological changes of brain tissue was more severe in DCI group,and the phosphorylated ERK1/2 levels were lower at 1,6,24,48 h (P ＜ 0.05) ;The Ku70 protein levels were lower at 1,6,24,48 h in DCI group (P ＜ 0.05) ; Compared with DCI group,the histopathological changes of neuronal necrosis and apoptosis was more severe in DCI + U0126 group; and the phosphorylated ERK1/2 expressions respectively decreased at 1,6,24,48 h (P ＜0.05) ;and the Ku70 protein levels were lower at 1,6,24,48 h (P ＜ 0.05).Conclusions U0126 enhanced the damage of nerve cells by inhibiting the activation of ERK1/2,thereby reducing the level of Ku70 protein in brain hippocampus of diabetic rats after global cerebral ischemia.