Background:Colonoscopy,regarded as the gold standard for detecting colorectal polyps,has a certain rate of missed diagnosis.Enhancing the polyp detection rate holds the promise of reducing the incidence of colorectal cancer.In recent years,electronic chromoendoscopy has been gradually gaining popularity.Optical enhancement(OE),which is the electron staining mode of Pentax endoscopy,and its impact on the polyp detection rate in patients with ulcerative colitis(UC)remains unclear.Aims:To investigate the effect of OE mode on polyp detection rate in patients with UC.Methods:A total of 233 UC patients who underwent colonoscopy at Xingtai People's Hospital in Hebei Province from July 2020 to April 2024 were enrolled.These patients were divided into the OE group and the High-definition white light(HDWL)group.The two groups were compared in terms of gender,age,Boston bowel preparation score(BBPS),withdrawal time,polyp detection rate,adenoma detection rate,polyp size,and polyp location.Results:There were no significant differences in gender,age,BBPS,and withdrawal time between the OE group and the HDWL group.When compared with the HDWL group,No significant differences in the polyp detection rate(24.66%vs.14.69%,P=0.071)and the adenoma detection rate(13.7%vs.6.99%,P=0.108)were found between the OE group and HDWL group.There was no significant difference in the detection rate of tiny polyps(with a diameter≤5 mm)between the OE group and the HDWL group(78.57%vs.79.41%,P=0.936).Also,there was no significant difference in the detection rate of proximal colon polyps(42.86%vs.41.18%,P=0.894).Moreover,no complications such as bleeding or perforation occurred during the colonoscopy in either group.Conclusions:During colonoscopy,compared with the HDWL mode,the OE mode does not significantly improve the polyp detection rate in UC patients.

Background:Colonoscopy,regarded as the gold standard for detecting colorectal polyps,has a certain rate of missed diagnosis.Enhancing the polyp detection rate holds the promise of reducing the incidence of colorectal cancer.In recent years,electronic chromoendoscopy has been gradually gaining popularity.Optical enhancement(OE),which is the electron staining mode of Pentax endoscopy,and its impact on the polyp detection rate in patients with ulcerative colitis(UC)remains unclear.Aims:To investigate the effect of OE mode on polyp detection rate in patients with UC.Methods:A total of 233 UC patients who underwent colonoscopy at Xingtai People's Hospital in Hebei Province from July 2020 to April 2024 were enrolled.These patients were divided into the OE group and the High-definition white light(HDWL)group.The two groups were compared in terms of gender,age,Boston bowel preparation score(BBPS),withdrawal time,polyp detection rate,adenoma detection rate,polyp size,and polyp location.Results:There were no significant differences in gender,age,BBPS,and withdrawal time between the OE group and the HDWL group.When compared with the HDWL group,No significant differences in the polyp detection rate(24.66%vs.14.69%,P=0.071)and the adenoma detection rate(13.7%vs.6.99%,P=0.108)were found between the OE group and HDWL group.There was no significant difference in the detection rate of tiny polyps(with a diameter≤5 mm)between the OE group and the HDWL group(78.57%vs.79.41%,P=0.936).Also,there was no significant difference in the detection rate of proximal colon polyps(42.86%vs.41.18%,P=0.894).Moreover,no complications such as bleeding or perforation occurred during the colonoscopy in either group.Conclusions:During colonoscopy,compared with the HDWL mode,the OE mode does not significantly improve the polyp detection rate in UC patients.

OBJECTIVE To investigate the change of tumor necrosis factor-α(TNF-α),interleukin-1β(IL-1β),intercellular adhesion molecules(ICAM-1),matrix metalloproteinases 2 (MMP-2) and MMP-9 contents in cultured pulmonary microvascular endothelial cells (PMVECs) in rats after perfluoroisobutylene (PFIB) exposure. METHODS PMVECs were separated and purified using a modified method of implantation of pulmonary tissues. After identification,PMVECs were divided into the normal control group and the PFIB-exposed groups(n=3). The PFIB-exposed groups inhaled PFIB at the concentration of 200 mg · m-3 for 5 min in a flow-past header,while the normal control group were PMVECs in quiescent condition. The supernatants and lysates of PMVECs were harvested at 0.5,1,2,4 and 8 h,respec?tively, after execution. The contents of TNF-α,IL-1β,ICAM-1,MMP-2 and MMP-9 were measured by ELISA,and the activity of MMP-2 and MMP-9 was measured by gelatin zymography. RESULTS① According to the morphologic characteristics of cell growth and the expression of specificity antigens and the bind experiment of phytohemagglutinin,the cells separated and purified by modified method shared the characteristics of PMVECs.②TNF-αwas rapidly expressed by PMVECs at 0.5 h post PFIB stimulation and the maximum value was achieved at 2 h post PFIB stimulation(P<0.05). The newly synthesized TNF-α was slowly released out of the cells. The maximum TNF-α in the supernatant was achieved at 4 h post stimulation.③Within 2 h of stimulation,PMVECs synthesized a large amount of IL-1β and peaks at 2 h. However,IL-1βwas never released to the extracellular milieu.④The amount of ICAM-1 was rapidly synthesized by PMVECs after PFIB stimulation,but at a low level.⑤After stimulation with PFIB,MMP-2 in the supernatant of PMVECs culture was gradually increased,peaked at 2 h and then decreased subsequently. The biological activity of MMP-2 in the supernatant was also enhanced after PFIB stimulation. PFIB did not stimulate synthesis or secretion of MMP-9,indicating that PMVECs were not the main source of MMP-9 during PFIB inhalation-induced acute lung injury. CONCLUSION PFIB stimulates the surviving PMVECs to synthesize a large amount of TNF-α,IL-1β, MMP-2 and conjunctive ICAM-1.

OBJECTlVE To establish Tg(-6.3CYP3A65∶EGFP) transgenic zebrafish for quick, intuitive detection of heavy metals ( copper, cadmium and zinc) , dioxin-like PCBs ( PCB126) and other environmental pollutants. METHODS Tol2 transposon system was used to generate transgenic zebrafish lines Tg(-6.3CYP3A65∶EGFP) in which CYP3A65 promoter regualated labeled fluorescence. The effect of heavy mentals ( copper, cadmium and zinc ) and PCB126 on the relative amounts of CYP3A65 gene expression was determined by observing the change in fluorescence intensity. RESULTS The relative gene expression of CYP3A65 was significantly increased after 96 h exposure to copper 0.1 and 0.2μmol·L-1 , cadmium 0.35 and 0.7μmol·L-1 , zinc 1.5 and 3μmol·L-1 , and PCB126 2-32μmol·L-1 , respectively ( P<0.01) , but decreased after 96 h exposure to copper 0. 9 μmol·L-1 , cadmium 2. 7 and 5.4 μmol·L-1 , and zinc 24μmol·L-1 , respectively( P<0.01) . CYP3A65 gene expression was significantly increased after 168 h exposure to copper 0.1 and 0.2 μmol·L-1 , cadmium 0.35 and 0.7 μmol·L-1 , zinc 1.5 and 3 μmol·L-1, and PCB126 2-32 μmol·L-1, respectively(P<0.01), but decreased after 168 h exposure to copper 0.9 μmol·L-1, cadmium 2.7 and 5.4 μmol·L-1, and zinc 12 and 24 μmol·L-1( P<0.05) , in a concentration-dependent manner. CONCLUSlON The results suggest that zebrafish CYP3A65 gene expression and the CYP3A65 labeled fluorescence lines can be another candidate biomarker for detecting environmental pollutants.

Objective To investigate tentatively the role of angiotensionⅡ( AngⅡ) in perfluoroisobutylene ( PFIB)-in-duced acute lung injury ( ALI) in rats.Methods Twenty-eight male Wistar rats were randomly divided into one control group(0 h) and six PFIB-exposed groups which were executed at 1, 2, 4, 8, 16 and 24 h after PFIB exposure (n=4). The PFIB-exposed groups inhaled PFIB at a concentration of 145 mg/m3 for 8 min in a flow-past header while the control group was exposed to the filtered air in a similar manner .After execution at the corresponding time-point, the samples of the lung, serum and brochoalveolar lavage fluid (BALF) were harvested.The measurement of the lung wet-to-dry weight ratio ( W/D) and total protein content in BALF , and the histopathological examination of the lung were carried out to evalu -ate the degree of lung injury .The over-time changes in the content of AngⅡin the lung homogenates and blood plasma and the activity of angiotensin converting enzyme ( ACE) in the lung tissue were observed .Results The lung W/D and total protein content in BALF were increased significantly at 16 h after PFIB exposure with severe acute lung edema and abun-dant neutrophil exudation to the alveoli , which were alleviated dramatically at 24 h after PFIB exposure .The content of AngⅡin the lung homogenate showed a tendency of increase during the first 8 hours with significant decrease at 16 and 24 h after exposure.However, the content of AngⅡin the plasma and the activity of ACE in the lung experienced of fluctuations , but without significant difference compared to the control group .Conclusion There is no obvious correlation between the extent of lung injury and that of AngⅡin the lung.The pathological significance of AngⅡin PFIB-induced ALI needs to be further clarified.

OBJECTIVE To investigate whether the pulmanary fibrosis formed after a single PFIB exposure.METHODS A total of 70 male mice were exposed to PFIB 130 mg·m-3 for 5 min.Pulmonary edema of 10 mice was evaluated by lung indices at 24 h after PFIB exposure.Pathological changes and collagen deposition were detected by hematoxylin and eosin (HE) and Sirius red stainings in the other mice,changes in collagen content in lungs and plasma by measuring the respective hydroxyproline content at 2,4,6,8,12 and 16 weeks after PFIB exposure.RESULTS Severe pulmonary edema was observed at 24 h after PFIB exposure.At day 14 after PFIB exposure,inflammatory cell infiltration,alveolar septum thickening,interstitial and alveolar edema and protein leakage were noticed.Collagens types Ⅰ and Ⅲ on the wall of vessel and bronchi were severely damaged,but considerable amount of collagen type Ⅲ deposited on the alveolar wall.The content of hydroxyproline considerably decreased in the lungs but increased significantly in the plasma up to six weeks.Hydroxyproline in lungs and plasma began to recover at the end of 8 weeks,and then returned to normal.At 16 weeks,they recovered to normal level.At the end of 4 weeks,the lung lesions and the collagens at the wall of vessel and bronchi began to recover gradually; collagen typeⅢ at the alveolar wall was gradually absorbed,too.At 16 weeks,the lungs almost recovered to normal level.CONCLUSION At earlier phase after PFIB exposure,the excessive collagens destruction in lungs is observed,but no pulmonary fibrosis forms at the later phase.