TISSUE AND WATER TISSUE CASE OF PORTABLE FOR ADVERTISING OR MARKETING

• 1. 用于组织病人胶片的案例隔板 [P] . 中国专利： CN101102907A . 2008-01-09
• 2. 用于将医疗器械附接到组织的附接装置、用于将医疗器械附接到组织的系统、具有附接装置的医疗器械、将医疗器械附接到组织的方法以及制造附接装置的方法 [P] . 中国专利： CN113766896A . 2021-12-07
• 3. PORTABLE WATER TISSUE SHOE POLISH IN WHICH A SHOE POLISH IS INJECTED TO A WATER TISSUE, AND A MANUFACTURING DEVICE THEREOF [P] . 韩国专利： KR20100007012A . 2010-01-22

  机译： 便携式抛光水鞋油在其中被擦伤的水组织及其制造装置

• 4. PORTABLE HUMIDIFICATION TISSUE AND TISSUE RACK WATER BOTTLE [P] . 韩国专利： KR20200057433A . 2020-05-26

  机译： 便携式加湿组织和组织架水瓶

• 5. PORTABLE OUTER CASING HAVING A WATER TANK CONTAINER FOR DRY TISSUE. [P] . 韩国专利： KR101534594B1 . 2015-07-08

  机译： 便携式外箱具有用于干组织的储水箱。

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• 1. BACKGROUND： Vibrio vulnifi cus inside the body could activate the NF-!B signaling pathwayand initiate the inflammatory cascade. The lung is one of the earliest organs affected by sepsisassociated with acute lung injury. High mobility group protein B1 （HMGB1） is an important late-actingpro-infl ammatory cytokine involving in the pathophysiology of sepsis. It is also involved in the injuryprocess in the lung, liver and intestine. There has been no report on the involvement of HMGB1 inVibrio vulnifi cus sepsis-induced lung injury.METHODS： Sixty rats were randomly divided into a normal control group （group A, n=10） anda Vibrio vulnificus sepsis group （group B, n=50）. Sepsis was induced in the rats by subcutaneousinjection of Vibrio vulnificus （concentration 6×108 cfu/mL, volume 0.1 mL/100g）） into the left lowerlimbs. The rats in group B were sacrifi ced separately 1, 6, 12, 24, and 48 hours after the infection.Their lungs were stored as specimens, lung water content was measured, and lung pathology wasobserved under a light microscope. The expressions of the HMGB1 gene and protein in the lungswere detected by RT-PCR and Western blot. Data were analyzed with one-way analysis of variance（ANOVA） and the LSD method for pair-wise comparison between the two groups. P〈0.05 wasconsidered statistically signifi cant.RESULTS： Compared to group A （0.652±0.177）, HMGB1 mRNA expression in the lungs ofgroup B was signifi cantly higher at 0 hour （1.161±0.358, P=0.013）, 24 hours （1.679±0.235, P=0.000）,and 48 hours （1.258±0.274, P=0.004） （P〈0.05）, and peaked at 24 hours. Compared to group A（0.594±0.190）, HMGB1 protein expression at 6 hours （1.408±0.567, P=0.026） after infection wassignificantly increased （P〈0. 05）, and peaked at 24 hours （2.415±1.064, P=0.000） after infection.Compared to group A （0.699±0.054）, lung water content was significantly increased at 6 hours（0.759±0.030, P=0.001）,12 hours （0.767±0.023, P=0.000）, 24 hours （0.771±0.043, P=0.000） and 48hours （0.789±0.137, P=0.000） after infection （P〈0.05）. Compared to group A, pathological changesat 12 hours in group B indicate marked pulmonary vascular congestion, interstitial edema andinfl ammatory infi ltration. Alveolar cavity collapse and boundaries of the alveolar septum could not beclearly identifi ed.CONCLUSION： Vibrio vulnifi cus sepsis can lead to injury in rat lungs, and increased HMGB1expression in lung tissue may be one of the mechanisms for injury from Vibrio vulnifi cus sepsis. [J] . Qiao-meng Qiu ,Zhong-wang Li ,Lu-ming Tang . 世界急诊医学杂志(英文) . 2011,第4期
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