In vitro and In vivo Activity of a New N-Oxide Derivative for Acne Vulgaris Treatment.

IF 1.9 4区 医学 Q3 CHEMISTRY, MEDICINAL
Ivone Leila Lima Delgado, Caue Benito Scarim, Felipe Hugo Alencar Fernandes, Karina Pereira Barbieri, Marisa Campos Polesi, Aline Renata Pavan, Diego Eidy Chiba, Herida Regina Nunes Salgado, Iracilda Zeppone Carlos, Marcos Antonio Correa, Cleverton Roberto de Andrade, Jean Leandro Dos Santos
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引用次数: 0

Abstract

Introduction: Furoxan and benzofuroxan are compounds containing an N-oxide function, known for their diverse pharmacological properties, including antimicrobial and antiinflammatory effects. This study aimed to investigate these activities using an in-house library of N-oxide compounds.

Method: Twenty compounds were tested against both Gram-positive and Gram-negative bacteria, including Cutibacterium acnes (C. acnes), a microorganism implicated in the development of acne vulgaris. One compound, (E)-4-(3-((2-(3-hydroxybenzoyl)hydrazone)methyl)phenoxy)-3- (phenylsulfonyl)-1,2,5-oxadiazol-2-N-oxide (compound 15), exhibited selective antimicrobial activity against C. acnes, with a Minimum Inhibitory Concentration (MIC) value of 2 μg/mL. Indirect measurement of Nitric Oxide (NO) release showed that compound 15 and isosorbide dinitrate, when treated with L-cysteine, produced nitrite levels of 20.1% and 9.95%, respectively. Using a NO scavenger (PTIO) in combination with compound 15 in a culture of C. acnes resulted in reduced antimicrobial activity, indicating that NO release is part of its mechanism of action. Cytotoxicity assessments using murine macrophages showed cellular viability above 70% at concentrations up to 0.78 μg/mL.

Results: Measurements of Interleukin-1 beta (IL1-β) and Tumor Necrosis Factor-alpha (TNF-α) indicated that compound 15 did not reduce the levels of these pro-inflammatory cytokines. Sustained NO production by inducible Nitric Oxide Synthase (iNOS) in macrophages or neutrophils has been found to be involved in the inflammatory process in acne vulgaris and lead to toxicity in surrounding tissues. Nitrite levels in the supernatant of murine macrophages were found to be decreased at a concentration of 0.78 μg/mL of compound 15, indicating an anti-inflammatory effect. In vivo studies were conducted using Balb/c nude mice inoculated subcutaneously with C. acnes. Cream and gel formulations of compound 15 were applied to treat the animals, along with commercially available anti-acne drugs, for 14 days. Animals treated with a cream base containing 5% of compound 15 exhibited less acanthosis with mild inflammatory infiltration compared to other groups, highlighting its anti-inflammatory properties.

Conclusion: Similar results were observed in the benzoyl peroxide group, demonstrating that compound 15 presented comparable anti-inflammatory activity to the FDA-approved drug. These promising results suggest that compound 15 has a dual mechanism of action, with selective antimicrobial activity against C. acnes and notable anti-inflammatory properties, making it a potential prototype for developing new treatments for acne vulgaris.

一种用于治疗痤疮的新型 N-氧化物衍生物的体外和体内活性。
简介呋喃酮和苯并呋喃酮是含有 N-氧化物功能的化合物,具有多种药理特性,包括抗菌和消炎作用。本研究旨在利用内部的 N-氧化物化合物库研究这些活性:测试了 20 种化合物对革兰氏阳性和革兰氏阴性细菌的作用,其中包括痤疮杆菌(Cutibacterium acnes,C. acnes),这是一种与寻常痤疮的发病有关的微生物。其中一种化合物(E)-4-(3-((2-(3-羟基苯甲酰基)腙)甲基)苯氧基)-3-(苯磺酰基)-1,2,5-恶二唑-2-N-氧化物(化合物 15)对痤疮丙酸杆菌具有选择性抗菌活性,最低抑菌浓度(MIC)为 2 微克/毫升。一氧化氮(NO)释放的间接测量表明,化合物 15 和二硝酸异山梨酯经 L-半胱氨酸处理后,产生的亚硝酸盐水平分别为 20.1%和 9.95%。在痤疮丙酸杆菌培养液中将 NO 清除剂(PTIO)与化合物 15 结合使用会降低其抗菌活性,这表明 NO 释放是其作用机制的一部分。使用小鼠巨噬细胞进行的细胞毒性评估显示,当浓度达到 0.78 μg/mL 时,细胞存活率超过 70%:结果:白细胞介素-1β(IL1-β)和肿瘤坏死因子-α(TNF-α)的测量结果表明,化合物 15 不会降低这些促炎细胞因子的水平。研究发现,巨噬细胞或中性粒细胞中的诱导型一氧化氮合成酶(iNOS)持续产生的一氧化氮参与了寻常痤疮的炎症过程,并导致周围组织中毒。研究发现,当化合物 15 的浓度为 0.78 μg/mL 时,小鼠巨噬细胞上清液中的亚硝酸盐水平会降低,这表明化合物 15 具有抗炎作用。使用 Balb/c 裸鼠皮下接种痤疮丙酸杆菌进行了体内研究。将化合物 15 的乳霜和凝胶制剂与市售的抗痤疮药物一起涂抹在动物身上,持续 14 天。与其他组相比,使用含 5%化合物 15 的乳膏基质治疗的动物表现出较少的黄褐斑和轻微的炎症浸润,这突出表明了化合物 15 的抗炎特性:结论:在过氧化苯甲酰组也观察到了类似的结果,这表明化合物 15 的抗炎活性与美国 FDA 批准的药物相当。这些令人鼓舞的结果表明,化合物 15 具有双重作用机制,既对痤疮丙酸杆菌具有选择性抗菌活性,又具有显著的抗炎特性,是开发治疗寻常痤疮新疗法的潜在原型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medicinal Chemistry
Medicinal Chemistry 医学-医药化学
CiteScore
4.30
自引率
4.30%
发文量
109
审稿时长
12 months
期刊介绍: Aims & Scope Medicinal Chemistry a peer-reviewed journal, aims to cover all the latest outstanding developments in medicinal chemistry and rational drug design. The journal publishes original research, mini-review articles and guest edited thematic issues covering recent research and developments in the field. Articles are published rapidly by taking full advantage of Internet technology for both the submission and peer review of manuscripts. Medicinal Chemistry is an essential journal for all involved in drug design and discovery.
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