1.Efficacy of sublingual immunotherapy with dermatophagoides farianae drops in the different age groups with allergic rhinitis
Yucheng YE ; Huijuan LIU ; Tong HUA ; Fuguo CAI
China Modern Doctor 2014;(30):22-24,30
Objective To evaluate the efficacy of the sublingual immunotherapy with Dermatophagoides farianae drops on different age groups. Methods The efficacy of 117 patients with AR received SLIT treatment for more than one year were retrospectively analyzed. These patients were divided into three groups according to the age,children group(6-14 year old,35 patients),youth age group(15-35 year old,45 cases)and middle-aged group(36-66 year old,37 pa-tients). Before and SLIT treatment for half one year, one year,symptom score, medication score and signs score were evaluated. Results After SLIT treatment for half a year and one year, the symptom score, medication score and signs score in these patients significantly reduced compared with before(P<0.05). Compared with after half a year treatment,the symptom score of children group significantly reduced(q=3.05,P<0.05),and other indicators were not statistically significant (P>0.05). The symptom score, medication score and signs score among three age groups were not statisti-cally significant (P>0.05) at all the time points. Conclusion Dermatophagoides farinae drops on allergic rhinitis can play a significant and similar effect in the different age groups.
2.Role of cathepsin B in mechanical ventilator-induced lung injury in rats: relationship with NLRP3 inflammasomes
Jiangxiao CAI ; Li CONG ; Boxi LIU ; Weiwei QIN ; Fuguo MA ; Lixin SUN ; Wei HAN
Chinese Journal of Anesthesiology 2022;42(4):475-480
Objective:To evaluate the role of cathepsin B (CTSB) in mechanical ventilator-induced lung injury (VILI) in rats and the relationship with NOD-like receptor pyrin domain containing 3 (NLRP3) inflammasome.Methods:Thirty-six SPF-grade healthy male Sprague-Dawley rats, aged 6-8 weeks, weighing 220-300 g, were divided into 3 groups ( n=12 each) by the random number table method: control group (group C), VILI group (group V) and VILI + CA074-me group (group Me). CA074-me 5 mg/kg was intraperitoneally injected in group Me, while the equal volume of normal saline was given instead in group C and group V. Group C kept spontaneous breathing for 4 h, and the animals were mechanically ventilated (tidal volume 20 ml/kg, respiratory rate 80 breaths/min, fraction of inspired oxygen 21%, PEEP 0 cmH 2O). Blood samples from femoral artery were collected for arterial blood gas analysis before tracheal intubation and after spontaneous breathing or ventilation, and PaO 2 was recorded.Rats were sacrificed, and bronchoalveolar lavage fluid (BALF) was collected and lung tissues were collected for determination of the wet/dry lung weight ratio (W/D ratio), serum interleukin-1beta (IL-1β) and IL-18 concentrations in BALF (by enzyme-linked immunosorbent assay), expression of CTSB, NLRP3, apoptosis-associated speck-like protein containing a caspase-1 recruitment domain (ASC) and caspase-1 mRNA in lung tissues (quantitative real-time polymerase chain reaction), and expression of CTSB, NLRP3, ASC and caspase-1 in lung tissues (by Western blot) and for microscopic examination of the pathological changes (using HE staining). Lung injury was assessed and scored. Results:Compared with group C, PaO 2 was significantly decreased after the end of ventilation, the lung injury score, W/D ratio and concentrations of IL-1β and IL-18 in serum and BALF were increased, and the expression of CTSB, NLRP3, ASC and caspase-1 protein and mRNA in lung tissues was up-regulated in group V and group Me ( P<0.01). Compared with group V, PaO 2 was significantly increased after the end of ventilation, the lung injury score, W/D ratio and concentrations of IL-1β and IL-18 in serum and BALF were decreased, and the expression of CTSB, NLRP3, ASC and caspase-1 protein and mRNA in lung tissues was down-regulated in group Me ( P<0.01). Conclusions:CTSB is involved in VILI in the rats, and the mechanism may be related to activation of NLRP3 inflammasomes.