Su X M, Ren Y, Kong L F, Kang J
Institute of Respiratory Disease, the First Affiliated Hospital of China Medical University, Shenyang 110001, China.
Zhonghua Nei Ke Za Zhi. 2017 Feb 1;56(2):121-126. doi: 10.3760/cma.j.issn.0578-1426.2017.02.008.
To investigate the therapeutic effects of givinostat, a histone deacetylase inhibitor (HDACI), on the development of chronic asthma with airway inflammation, airway remodeling and airway hyperresponsiveness (AHR). BALB/C mice were randomly divided into control group, asthma group, dexamethasone group and givinostat group (=12 per group). AHR was assessed. Total cell numbers and differential counts, interleukin-4(IL-4), interleukin-5(IL-5) and interferon-γ (IFNγ) levels in the bronchoalveolar lavage fluid (BALF) were measured in the above 4 groups. The pathology of lung tissue was evaluated. Immunohistochemical (IHC) staining and Western blot were used to detect α smooth muscle actin(α-SMA) and transforming growth factor-β1(TGFβ1). Compared with the asthma only group, givinostat treatment relieved airway resistance (2.96±1.01 vs 6.50±0.79, <0.05). Total inflammatory cells [(33.04±5.62)×10(4)/ml vs (98.04±9.27)×10(4)/ml, <0.01], eosinophil cells [(9.17±2.33)×10(4)/ml vs(37.64±6.98)×10(4)/ml, <0.01], IL-4 [(10.12±2.98)ng/ml vs (16.88±2.78)ng/ml, <0.05] and IL-5 [(27.09±3.62)ng/ml vs (37.86±7.34)ng/ml, <0.05] levels were all reduced in givinostat group, while IFNγ [(91.86±23.73)pg/ml vs (60.49±11.88)pg/ml, >0.05] was enhanced in BALF. Inflammatory cell infiltration around the airway was reduced, with decreased inflammatory cell score[(1.60±0.69)points vs (3.40±0.68) points, <0.01] and inflammatory cell number (111.65±31.41 vs 601.25±186.85, <0.01). The goblet cell metaplasia [(26.36±2.33)% vs (57.21±11.56)%] and collagen deposition area [(52.77±7.58)μm(2)/μm vs (111.81±12.40)μm(2)/μm] were obviously reduced (<0.01). The expressions of α-SMA and TGFβ1 in the lung tissue were both significantly decreased (<0.01). Givinostat treatment can reduce airway inflammation, airway remodeling and airway hyperresponsiveness in chronic asthma. Its effect is comparable to that of glucocorticoid hormone treatment.
为研究组蛋白去乙酰化酶抑制剂(HDACI)吉维司他对慢性哮喘伴气道炎症、气道重塑和气道高反应性(AHR)发展的治疗作用。将BALB/C小鼠随机分为对照组、哮喘组、地塞米松组和吉维司他组(每组n = 12)。评估AHR。检测上述4组支气管肺泡灌洗液(BALF)中的总细胞数及分类计数、白细胞介素-4(IL-4)、白细胞介素-5(IL-5)和干扰素-γ(IFNγ)水平。评估肺组织病理学。采用免疫组织化学(IHC)染色和蛋白质印迹法检测α平滑肌肌动蛋白(α-SMA)和转化生长因子-β1(TGFβ1)。与单纯哮喘组相比,吉维司他治疗可减轻气道阻力(2.96±1.01 vs 6.50±0.79,P<0.05)。吉维司他组BALF中的总炎性细胞[(33.04±5.62)×10⁴/ml vs (98.04±9.27)×10⁴/ml,P<0.01]、嗜酸性粒细胞[(9.17±2.33)×10⁴/ml vs (37.64±6.98)×10⁴/ml,P<0.01]、IL-4[(10.12±2.98)ng/ml vs (16.88±2.78)ng/ml,P<0.05]和IL-5[(27.09±3.62)ng/ml vs (37.86±7.34)ng/ml,P<0.05]水平均降低,而IFNγ[(91.86±23.73)pg/ml vs (60.49±11.88)pg/ml,P>0.05]升高。气道周围炎性细胞浸润减少,炎性细胞评分[(1.60±0.69)分vs (3.40±0.68)分,P<0.01]和炎性细胞数量(111.65±31.41 vs 601.25±186.85,P<0.01)降低。杯状细胞化生[(26.36±2.33)% vs (57.21±11.56)%]和胶原沉积面积[(52.77±7.58)μm²/μm vs (111.81±12.40)μm²/μm]明显减少(P<0.01)。肺组织中α-SMA和TGFβ1的表达均显著降低(P<0.01)。吉维司他治疗可减轻慢性哮喘的气道炎症、气道重塑和气道高反应性。其效果与糖皮质激素治疗相当。