Anti-Inflammatory Actions of Expectorants in a Rat Carrageenan-Induced Footpad Edema Model.

IF 1.5 4区 医学 Q4 CHEMISTRY, MEDICINAL
Pharmazie Pub Date : 2023-07-01 DOI:10.1691/ph.2023.3528
M Ito, X Liu, K Taguchi, Y Enoki, Y Kuroda, J Kizu, K Matsumoto
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引用次数: 0

Abstract

S-Carboxymethyl-L-cysteine (SCMS) exhibits sputum-regulating and anti-inflammatory actions. Previous studies reported the anti-inflammatory effects of SCMS on chronic inflammatory diseases, but no study has examined these effects on acute inflammatory diseases. In this study, we investigated the anti-inflammatory effects of SCMS in a rat carrageenan-induced footpad edema model, which is routinely used as an acute inflammation model. Expectorants were administered to rats with footpad edema induced by subcutaneously administering 1%λ-carrageenan to the footpad of the left posterior limb, and the dose dependency of the anti-inflammatory effects was evaluated. As a result, even when the dose of SCMS was increased to 400 mg/kg, there were no inhibitory effects on edema. Furthermore, we examined the inhibitory effects of other expectorants (ambroxol hydrochloride, N-acetyl-L-cysteine, L-cysteine ethylester hydrochloride, and L-cysteine methylester hydrochloride), which were reported to exhibit anti-inflammatory effects on chronic inflammation, on edema. However, none of these expectorants inhibited edema.

祛痰剂对卡拉胶致大鼠足垫水肿模型的抗炎作用。
s -羧甲基- l-半胱氨酸(SCMS)具有调节痰液和抗炎作用。以往的研究报道了SCMS对慢性炎性疾病的抗炎作用,但尚未有研究证实SCMS对急性炎性疾病的抗炎作用。在本研究中,我们研究了SCMS对卡拉胶诱导的大鼠足垫水肿模型的抗炎作用,该模型通常被用作急性炎症模型。左后肢足垫皮下注射1%λ-卡拉胶致足垫水肿大鼠给予祛痰剂,并评价其抗炎作用的剂量依赖性。因此,即使SCMS剂量增加到400 mg/kg,对水肿也没有抑制作用。此外,我们还研究了其他祛痰剂(盐酸氨溴索、n -乙酰- l-半胱氨酸、l-半胱氨酸乙酯盐酸盐和l-半胱氨酸甲基乙酯盐酸盐)的抑制作用,据报道,这些祛痰剂对慢性炎症和水肿具有抗炎作用。然而,这些祛痰药都不能抑制水肿。
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来源期刊
Pharmazie
Pharmazie 医学-化学综合
CiteScore
3.10
自引率
0.00%
发文量
56
审稿时长
1.2 months
期刊介绍: The journal DiePharmazie publishs reviews, experimental studies, letters to the editor, as well as book reviews. The following fields of pharmacy are covered: Pharmaceutical and medicinal chemistry; Pharmaceutical analysis and drug control; Pharmaceutical technolgy; Biopharmacy (biopharmaceutics, pharmacokinetics, biotransformation); Experimental and clinical pharmacology; Pharmaceutical biology (pharmacognosy); Clinical pharmacy; History of pharmacy.
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