Perić Aleksandar, Vezmar Kovačević Sandra, Barać Aleksandra, Gaćeša Dejan, Perić Aneta V, Vojvodić Danilo
Department of Otorhinolaryngology, Military Medical Academy Faculty of Medicine, University of Defense, Belgrade, Serbia.
Medigroup General Hospital, Belgrade, Serbia.
J Drug Assess. 2020 Nov 4;9(1):145-150. doi: 10.1080/21556660.2020.1838176.
Previous investigations suggest the use of extract from the roots of (EPs 7630) for improvement of the symptoms of uncomplicated upper airway inflammations, due to its antimicrobial and immunomodulatory actions. The aim of this investigation was to evaluate the effects of EPs 7630 on chemokine production in nasal mucosa and clinical parameters of patients with acute postviral rhinosinusitis (APRS).
Twenty-six ( = 26) APRS patients and 25 ( = 25) control subjects were included in this prospective study. We measured the concentrations of thirteen chemokines in nasal secretions of APRS patients and controls by flow cytometry. The patients with APRS were treated by EPs 7630 20 mg oral tablets, three times daily for 10 days. We compared the chemokine levels in nasal secretions, nasal symptoms and endoscopic findings in patients, before and after therapy.
We found higher Total Symptom Score (TSS) and higher concentrations of MCP-1, MIP-1α, MIP-1β, MIP-3α, ENA-78 and IL-8 in nasal secretions of APRS patients than in controls. After therapy by EPs 7630, we found significant improvement in all symptoms and endoscopic findings of APRS. The concentrations of MCP-1, IP-10 and MIP-1β were significantly increased and levels of MIP-1α, ENA-78, GROα and IL-8 significantly decreased in nasal fluid samples after therapy. No adverse effects were reported during the treatment.
Our results suggest the presence of modulatory effects of EPs 7630 on production of chemokines regulating the function of neutrophils and monocytes in the site of inflammation of the nasal mucosa in patients with APRS.
先前的研究表明,由于其抗菌和免疫调节作用,(EPs 7630)的根提取物可用于改善单纯性上呼吸道炎症的症状。本研究的目的是评估EPs 7630对急性病毒性鼻-鼻窦炎(APRS)患者鼻黏膜趋化因子产生及临床参数的影响。
本前瞻性研究纳入了26例(n = 26)APRS患者和25例(n = 25)对照受试者。我们通过流式细胞术测量了APRS患者和对照受试者鼻分泌物中13种趋化因子的浓度。APRS患者接受EPs 7630 20mg口服片剂治疗,每日3次,共10天。我们比较了患者治疗前后鼻分泌物中的趋化因子水平、鼻部症状和内镜检查结果。
我们发现APRS患者鼻分泌物中的总症状评分(TSS)以及MCP-1、MIP-1α、MIP-1β、MIP-3α、ENA-78和IL-8浓度均高于对照组。经EPs 7630治疗后,我们发现APRS的所有症状和内镜检查结果均有显著改善。治疗后鼻液样本中MCP-1、IP-10和MIP-1β的浓度显著升高,而MIP-1α、ENA-78、GROα和IL-8的水平显著降低。治疗期间未报告不良反应。
我们的结果表明,EPs 7630对APRS患者鼻黏膜炎症部位调节中性粒细胞和单核细胞功能的趋化因子产生具有调节作用。