Wei Wei, Cao Tingting, Pathak Janak L, Liu Xintong, Mao Tianjiao, Watanabe Nobumoto, Li Xiaomeng, Zhang Manli, Li Jiang
The Key Laboratory of Molecular Epigenetic, Institute of Genetics and Cytology, Northeast Normal University, Changchun, China.
Guangdong Engineering Research Center of Oral Restoration and Reconstruction, Affiliated Stomatology Hospital of Guangzhou Medical University, Guangzhou, China.
Front Pharmacol. 2022 Feb 21;13:818116. doi: 10.3389/fphar.2022.818116. eCollection 2022.
Xerostomia is a common symptom in menopausal women, suggesting the role of sex steroids in disease development. Shreds of literature had reported the potential use of herbal extracts to relieve xerostomia. However, a cocktail of multiple components in herbal extract makes it difficult to understand the exact mechanism of action. Aquaporin5 (AQP5), the specific aquaporin expressed in salivary glands, plays an important role in salivary secretion as a downstream of estrogen signaling. In this study, we aimed to unravel a single active herbal component as a therapeutic for xerostomia and investigate its mechanism of action. The effects of apigenin (flavonoid), dauricine (alkaloids), protopine (alkaloids), and lentinan (polysaccharides) on AQP5 transcription were screened . Only apigenin robustly induced AQP5 transcription and expression, and this effect was even robust compared to the effect of estradiol (E2, a positive control). Overexpression of estrogen receptor (ERα) in the human salivary gland cell line (HSG) upregulated the AQP5 transcription and expression and the knockdown ERα reversed this effect, suggesting the role of ERα signaling on AQP5 activation in HSG cells. Docking results showed apigenin-specific binding sites in ERα. We further analyzed the therapeutic effect of apigenin on ovariectomized mice as a xerostomia model. The saliva secretion in the xerostomia group was reduced to one-third of the sham group, whereas the apigenin or E2 treatment for 12 weeks reversed this effect. Meanwhile, the water consumption in the xerostomia group was augmented obviously compared to the sham group, whereas the water consumption in the apigenin and E2 group was declined to the level of the sham group. Immunohistochemistry of submandibular glands revealed the downregulation of AQP5 expression in xerostomia mice compared to control. Apigenin, or E2 treatment, upregulated AQP5 expression in xerostomia mice. In conclusion, apigenin, a single active component of herbal extract, upregulated AQP5 expression in HSG cells via activation of ERα signaling and restored saliva flow rates in OVX mice. These results revealed apigenin as a single active component of herbal extract with the potential to treat xerostomia.
口干症是绝经后女性的常见症状,提示性类固醇在疾病发展中的作用。已有文献报道了草药提取物缓解口干症的潜在用途。然而,草药提取物中的多种成分混合物使得难以理解其确切的作用机制。水通道蛋白5(AQP5)是唾液腺中表达的特异性水通道蛋白,作为雌激素信号的下游在唾液分泌中起重要作用。在本研究中,我们旨在找出一种单一的活性草药成分作为口干症的治疗药物,并研究其作用机制。筛选了芹菜素(黄酮类)、蝙蝠葛碱(生物碱)、原阿片碱(生物碱)和香菇多糖(多糖)对AQP5转录的影响。只有芹菜素能强烈诱导AQP5的转录和表达,与雌二醇(E2,阳性对照)相比,这种作用甚至更强。人唾液腺细胞系(HSG)中雌激素受体α(ERα)的过表达上调了AQP5的转录和表达,而敲低ERα则逆转了这种作用,提示ERα信号在HSG细胞中对AQP5激活的作用。对接结果显示芹菜素在ERα中有特异性结合位点。我们进一步分析了芹菜素对去卵巢小鼠作为口干症模型的治疗效果。口干症组的唾液分泌减少至假手术组的三分之一,而芹菜素或E2治疗12周可逆转这种作用。同时,口干症组的饮水量明显高于假手术组,而芹菜素和E2组的饮水量降至假手术组水平。下颌下腺的免疫组织化学显示,与对照组相比,口干症小鼠中AQP5表达下调。芹菜素或E2治疗可上调口干症小鼠中AQP5的表达。总之,芹菜素作为草药提取物的单一活性成分,通过激活ERα信号上调了HSG细胞中AQP5的表达,并恢复了去卵巢小鼠的唾液流速。这些结果表明芹菜素是草药提取物中具有治疗口干症潜力的单一活性成分。