蔡霈 文曉柯 歐陽(yáng)波 肖作奇
[摘要] 目的 研究地膚子總黃酮(FFK)對(duì)二硝基氯苯(DNBC)致大鼠變態(tài)反應(yīng)性接觸性皮炎(ACD)的抗炎作用。方法 SPF級(jí)SD大鼠40只,雌雄各半,按隨機(jī)數(shù)字表法分為五組,每組8只,即空白對(duì)照組、ACD模型組、陽(yáng)性藥對(duì)照組(醋酸潑尼松龍2.5 mg/kg)、FFK低劑量組(75 mg/kg)、FFK高劑量組(150 mg/kg);以DNBC建立大鼠ACD模型后,予以FFK灌胃給藥,連續(xù)10 d。觀察皮膚變態(tài)性反應(yīng)和腫脹度,同時(shí)測(cè)定血清中白細(xì)胞介素-6(IL-6)、白細(xì)胞介素-10(IL-10)和γ干擾素(IFN-γ)表達(dá)水平,并通過(guò)免疫組化檢測(cè)耳組織中核因子κB p65(NF-κB p65)表達(dá)水平。 結(jié)果 與空白對(duì)照組比較,ACD模型組大鼠皮膚腫脹度明顯增高,血清中IL-6、IFN-γ含量與耳組織中NF-κB p65蛋白表達(dá)明顯增高,而血清中IL-10含量明顯降低(P < 0.01);與ACD模型組比較,F(xiàn)FK低劑量組與FFK高劑量組大鼠的耳腫脹度、血清中IL-6、IFN-γ含量、耳組織中NF-κB p65蛋白表達(dá)水平顯著降低(P < 0.01),而血清中IL-10含量顯著升高(P < 0.01)。 結(jié)論 FFK對(duì)于DNBC致大鼠ACD具有抗炎作用,其機(jī)制可能是通過(guò)抑制NF-κB p65蛋白發(fā)揮作用。
[關(guān)鍵詞] 地膚子總黃酮;炎癥;接觸性皮炎;核轉(zhuǎn)錄因子-κB p65
[中圖分類號(hào)] R758.22? ? ? ? ? [文獻(xiàn)標(biāo)識(shí)碼] A? ? ? ? ? [文章編號(hào)] 1673-7210(2019)07(b)-0017-04
Anti-inflammatory effect of the total flavonoids of Fructus Kochiae in DNBC-induced allergic contact dermatitis rats
CAI Pei? ?WEN Xiaoke? ?OUYANG Bo? ?XIAO Zuoqi
Department of Pharmaceutical Research, Hu′nan Provincial Maternal and Child Health Care Hospital, Hu′nan Province, Changsha? ?410008, China
[Abstract] Objective To investigate the anti-inflammatory effect of the total flavonoids of Fructus Kochiae (FFK) on DNBC-induced allergic contact dermatitis (ACD) rats. Methods According to random number table method, 40 half male and half female SPF grade SD rats were randomly divided into 5 groups, with 8 rats in each group, including blank control group, ACD model group, positive control group (Splash Methylprednisolone 2.5 mg/kg), FFK low-dose group (75 mg/kg), FFK high-dose group (150 mg/kg). After ACD model were established by treatment of DNCB on right ear for 10 days, rats were treated with FFK in 10 d and the allergic reaction and swelling degree of ears were observed, the content of IL-6, IL-10 and IFN-γ in serum and the level of NF-κB p65 in ears were determined. Results Compared with the blank control group, the swelling of ears in ACD model group was significantly increased, the content of IL-6, IFN-γ in serum and the level of NF-κB p65 in ears were up-regulated, while the content of IL-10 was down-regulated in serum (P < 0.01). Compared with the ACD model group, the ears swelling degree of rats in FFK low-dose group and FFK high-dose group was significantly decreased, the content of IL-6, IFN-γ in serum and the level of NF-κB p65 in ears were significantly down-regulated, while the content of IL-10 in serum was significantly up-regulated (P < 0.01). Conclusion FFK has anti-inflammatory effect on DNBC-induced ADC rats and its mechanism involved in down-regulate the NF-κB p65.
[Key words] Total flavonoids of Fructus Kochiae; Inflammation; Allergic contact dermatitis; NF-κB p65
地膚子為黎科植物地膚Kochia Scoparia (L.) Schrad.的干燥成熟果實(shí),其性寒、味甘苦,具有清熱利濕、祛風(fēng)止癢等功效,常用于小便澀痛、陰癢帶下、皮膚瘙癢、濕疹等病癥[1]。現(xiàn)代醫(yī)學(xué)研究證明,地膚子具有抗氧化、抗過(guò)敏、抗病原微生物等作用[3-7]。地膚子主要含有黃酮及皂苷類成分,皂苷類成分近年來(lái)研究較多,而對(duì)于黃酮類的成分卻鮮見(jiàn)報(bào)道。目前,地膚子黃酮類成分的藥理作用研究?jī)H限于其體外抗氧化活性[8-9]。本研究通過(guò)建立二硝基氯苯(DNBC)誘導(dǎo)的大鼠變態(tài)反應(yīng)性接觸性皮炎(ACD)評(píng)價(jià)地膚子總黃酮(total flavonoids of Fructus Kochiae,F(xiàn)FK)對(duì)其治療作用,觀察FFK對(duì)于大鼠ACD的治療作用并對(duì)其作用機(jī)制進(jìn)行初步探討。
1 材料與方法
1.1 材料
1.1.1 實(shí)驗(yàn)動(dòng)物? SPF級(jí)SD大鼠,雌雄各半,體重50~60 g,購(gòu)于湖南斯萊克景達(dá)實(shí)驗(yàn)動(dòng)物有限公司,許可證號(hào):SCXK(湘)2011-0003。動(dòng)物合格證號(hào)為:NO.4300470013754。飼養(yǎng)于湖南師范大學(xué)醫(yī)學(xué)院實(shí)驗(yàn)動(dòng)物中心,自由進(jìn)食及飲水,實(shí)驗(yàn)室溫度(22±2)℃,濕度60%~80%,人工光照約12 h∶12 h明暗周期。
1.1.2 藥品與試劑? 醋酸潑尼松龍片(規(guī)格1片∶5 mg)購(gòu)于天方藥業(yè)有限公司,生產(chǎn)批號(hào):180211135;2,4-硝基氯苯(2,4-DNCB),購(gòu)于山東西亞化學(xué)股份有限公司,生產(chǎn)批號(hào):W5784;IL-6(貨號(hào):F3066-A)、白細(xì)胞介素-10(IL-10,貨號(hào):F3071-A)、TNF-α(貨號(hào):F3056-A)均購(gòu)于上??婆d生物科技有限公司;核轉(zhuǎn)錄因子-κB p65(NF-κB p65)大鼠抗體(貨號(hào):ARG65677)購(gòu)于上海雅吉生物科技有限公司;蘆丁購(gòu)自上海詩(shī)丹德生物技術(shù)有限公司,生產(chǎn)批號(hào):153-18-4,純度為99.8%;乙醇、丙酮均為國(guó)產(chǎn)分析純,購(gòu)自國(guó)藥集團(tuán);地膚子購(gòu)于湖南衡東縣中藥飲片廠,生產(chǎn)批號(hào):20170428,經(jīng)湖南省中醫(yī)院藥學(xué)部王竹鑫主任藥師鑒定為黎科植物地膚的干燥成熟果實(shí),各項(xiàng)規(guī)定均符合2015年版《中華人民共和國(guó)藥典》[1]。
1.1.3 儀器設(shè)備? Leica RM2235型萊卡石蠟切片機(jī)(德國(guó)萊卡);SEN-CO W201恒溫水浴鍋(上海申生科技有限公司);5424R高速離心機(jī)(Eppendorf);DP72奧林巴斯顯微成像系統(tǒng);RT-6100酶標(biāo)分析儀(深圳雷杜生命科學(xué)股份有限公司);XS205型電子天平(德國(guó)梅特勒-托利多)。
1.2 方法
1.2.1 地膚子總黃酮的制備? 地膚子粉碎后經(jīng)80%乙醇提取,經(jīng)大孔樹(shù)脂富集減壓干燥所得棕色粉末即為FFK,以蘆丁為標(biāo)準(zhǔn)品,應(yīng)用NaNO2-Al(NO3)3-NaOH反應(yīng)體系測(cè)得其含量為85.64%總黃酮有效部位。
1.2.2 DNCB誘導(dǎo)的大鼠ACD模型建立? 將丙酮與橄欖油按4∶1的體積比混合均勻,加入不同質(zhì)量的DNCB使其溶解,最后配制成1%和7%的DNCB溶液。首先將7% DNCB溶液涂抹于大鼠腹部除毛處進(jìn)行腹部致敏,之后改用1% DNCB溶液增強(qiáng)致敏。5 d后將1% DNCB溶液涂抹于大鼠右耳,連續(xù)3 d,即建立DNCB誘導(dǎo)的ACD大鼠模型[10]。
1.2.3 地膚子總黃酮對(duì)ACD大鼠的抗炎作用? 取8只正常大鼠為空白對(duì)照組,取40只ACD大鼠按隨機(jī)數(shù)字表法分為ACD模型組、陽(yáng)性藥對(duì)照組(醋酸潑尼松龍2.5 mg/kg)、FFK低劑量組(75 mg/kg)、FFK高劑量組(150 mg/kg),每組8只;各組灌胃給藥10 d后(空白對(duì)照組與DNCB模型組予以等體積1% CMC-Na,其余各組藥物均以1% CMC-Na混懸),以8 mm穿孔器右耳組織,并用千分尺測(cè)量厚度評(píng)價(jià)鼠耳腫脹程度。同時(shí)各組取4只大鼠耳組織石蠟包埋切片然后進(jìn)行HE染色分析。
1.2.4 酶聯(lián)免疫吸附試驗(yàn)(ELISA)測(cè)定大鼠血液中的炎癥因子? 腹主動(dòng)脈采集上述給藥10 d后的大鼠血液樣本2 mL,室溫靜置30 min后,于4℃,3000 r/min離心10 min,收集血清樣本于-80℃冰箱保存。參照試劑盒說(shuō)明書(shū)用ELISA法檢測(cè)血清中白細(xì)胞介素-6(IL-6)、IL-10和γ干擾素(IFN-γ)含量。
1.2.5 免疫組化評(píng)價(jià)? 檢測(cè)大鼠耳組織中的NF-κB p65的蛋白表達(dá)水平。取“1.2.2”石蠟切片進(jìn)行免疫組化分析。即經(jīng)脫蠟固定后,加入NF-κB p65一抗(1∶500)、二抗孵育,之后染色封片,應(yīng)用Image-Pro Plus 6.0對(duì)結(jié)果進(jìn)行分析,數(shù)據(jù)以各組積分光密度均值與空白對(duì)照組比值表示。
1.3 統(tǒng)計(jì)學(xué)方法
采用SPSS 17.0統(tǒng)計(jì)學(xué)軟件進(jìn)行數(shù)據(jù)分析,計(jì)量資料用均數(shù)±標(biāo)準(zhǔn)差(x±s)表示,多組間比較采用單因素方差分析(One-way ANOVA)和Dunnett′s t檢驗(yàn)進(jìn)行組間比較。以P < 0.05為差異有統(tǒng)計(jì)學(xué)意義。
2 結(jié)果
2.1 FFK對(duì)ACD大鼠耳腫脹度的影響
經(jīng)10 d的藥物治療后,與空白對(duì)照組比較,ACD模型組大鼠右耳仍呈明顯的紅腫狀態(tài),而陽(yáng)性藥對(duì)照組大鼠經(jīng)潑尼松治療后基本恢復(fù)正常,F(xiàn)FK低、高劑量組均有效改善了大鼠右耳的紅腫狀態(tài)。與空白對(duì)照組比較,ACD模型組大鼠耳厚和耳重明顯增加(P < 0.01);與ACD模型組比較,F(xiàn)FK高、低劑量組大鼠耳厚和耳重顯著降低(P < 0.01)。見(jiàn)表1。
2.2 大鼠耳組織病理學(xué)觀察
與空白對(duì)照組比較,經(jīng)DNCB誘導(dǎo)的ACD模型大鼠耳組織切片HE染色顯示其單核細(xì)胞出現(xiàn)明顯浸潤(rùn),表皮細(xì)胞呈角質(zhì)化,耳組織可見(jiàn)明顯腫脹,而FFK高、低劑量組與陽(yáng)性藥對(duì)照組可見(jiàn)其耳組織的紅腫與炎癥狀態(tài)有明顯改善。見(jiàn)圖1。
2.3 FFK對(duì)ACD大鼠血清中炎癥因子IL-6、IL-10與IFN-γ的影響
免疫共沉淀結(jié)果顯示,與空白對(duì)照組比較,ACD模型組大鼠血清中IL-6、IFN-γ的含量顯著升高(P < 0.01),而IL-10的含量明顯降低(P < 0.01),提示ACD模型大鼠發(fā)生了嚴(yán)重的炎性反應(yīng)。而經(jīng)過(guò)FFK治療后的ACD模型大鼠其血清中IL-6與IFN-γ含量顯著降低(P < 0.01),IL-10顯著升高(P < 0.01),提示FFK能夠有效治療ACD模型大鼠的炎性反應(yīng)。見(jiàn)圖2。
2.4 FFK對(duì)ACD大鼠NF-κB p65表達(dá)的影響
免疫組化分析結(jié)果顯示,與空白對(duì)照組比較,ACD模型組大鼠耳組織NF-κB p65蛋白表達(dá)顯著上調(diào),差異有高度統(tǒng)計(jì)學(xué)意義(P < 0.01);與ACD模型組比較,F(xiàn)FK低、高劑量組能夠下調(diào)由DNCB誘導(dǎo)的大鼠耳組織NF-κB p65表達(dá),差異有高度統(tǒng)計(jì)學(xué)意義(P < 0.01)。見(jiàn)圖3~4。
3 討論
炎癥是多種疾病的基本病理過(guò)程,人類的許多常見(jiàn)疾病如各種病原體感染(肝炎、結(jié)核病等)、自身免疫性疾病、皮炎濕疹等都屬于炎癥范疇。炎癥的發(fā)生過(guò)程不僅與炎癥相關(guān)酶、炎癥介質(zhì)、細(xì)胞因子有關(guān),還涉及核因子-κB、一氧化氮、自由基的參與。NF-κB是細(xì)胞炎癥以及多種自身免疫性疾病調(diào)節(jié)的關(guān)鍵蛋白[11-13]。它在應(yīng)激條件下能夠刺激輔助性T細(xì)胞產(chǎn)生IL-2、IL-6、IL-10以及IFN-γ等炎癥因子[14-17],如IFN-γ能夠活化巨噬細(xì)胞,繼而釋放多種炎癥介質(zhì)[18-19]。DNCB能夠與上皮蛋白可溶性部分共價(jià)結(jié)合成為完全抗原,已廣泛應(yīng)用于建立ACD模型,其機(jī)制為誘導(dǎo)皮膚組織的T細(xì)胞浸潤(rùn),包括Th1誘導(dǎo)的遲發(fā)型超敏反應(yīng)和Th2誘導(dǎo)的過(guò)敏反應(yīng),而這一反應(yīng)激活了下游的IL-6、IFN-γ等炎癥因子[20-22]。
對(duì)于炎癥的治療,常用糖皮質(zhì)激素類甾體抗炎藥和非甾體抗炎藥,前者易產(chǎn)生依賴性,且易引起腎上腺皮質(zhì)功能衰退等不良反應(yīng),后者的胃腸道不良反應(yīng)普遍,因此從天然藥物中開(kāi)發(fā)抗炎藥物受到廣泛關(guān)注。本研究發(fā)現(xiàn),經(jīng)DNCB誘導(dǎo)的ACD模型大鼠,其耳組織厚度、重量以及HE染色結(jié)果均表明耳組織發(fā)生腫脹與炎性反應(yīng),ACD模型大鼠血清中檢測(cè)到IL-6和IFN-γ含量升高,IL-10含量降低,而耳組織中同樣可見(jiàn)NF-κB p65蛋白表達(dá)上調(diào),這說(shuō)明大鼠處于應(yīng)激狀態(tài)發(fā)生了嚴(yán)重的炎性反應(yīng)。FFK能夠顯著降低ACD大鼠的耳組織腫脹,下調(diào)血清中IL-6和IFN-γ,上調(diào)IL-10,同時(shí)抑制耳組織中NF-κB p65蛋白的表達(dá),提示FFK對(duì)于NF-κB p65具有顯著的下調(diào)作用,而這一下調(diào)作用在ACD模型大鼠中表現(xiàn)為抗炎藥理活性。上述結(jié)果提示,F(xiàn)FK對(duì)于DNCB誘導(dǎo)的ACD大鼠炎性反應(yīng)具有明顯的改善作用,其可能通過(guò)下調(diào)NF-κB p65表達(dá),抑制炎癥相關(guān)因子從而發(fā)揮抗炎作用。
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