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Toxicol Lett ; 349: 145-154, 2021 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-34126182

RESUMEN

Cutaneous eruptions caused by the combination of Chinese and Western medicine have attracted widespread attention; however, the underlying mechanism remains unclear. This study aimed to evaluate the potential mechanism of cutaneous eruptions in vivo and in vitro using the combination of Shuanghuanglian injection powder (SHL) and aspirin (ASA) as an example. ASA and SHL co-administration induced inflammatory responses in HaCat cells, as evidenced by marked increases in the expression of IL-4 and TNF-α, and the level of apoptosis. Additionally, histopathological investigation of mice skin tissues showed local inflammatory cell infiltration. Western boltting was used to detect the effects of ASA on desmoglein-1 (DSG1) expression; we found that DSG1 expression was down-regulated in vivo and in vitro. Finally, the key components of SHL were administered to HaCat cells with down-regulated DSG1; it was seen that neochlorogenic acid and rutin have a significant effect on HaCat cell apoptosis. These results demonstrate that DSG1 deficiency is a potential cause of cutaneous eruptions caused by the combination of SHL and ASA, and neochlorogenic acid and rutin are the main allergenic components. This study provides a new research strategy for the safety evaluation of integrated traditional Chinese and Western medicine.


Asunto(s)
Apoptosis/efectos de los fármacos , Aspirina/toxicidad , Desmogleína 1/antagonistas & inhibidores , Erupciones por Medicamentos/etiología , Medicamentos Herbarios Chinos/toxicidad , Queratinocitos/efectos de los fármacos , Animales , Ácido Clorogénico/análogos & derivados , Ácido Clorogénico/toxicidad , Desmogleína 1/metabolismo , Erupciones por Medicamentos/metabolismo , Erupciones por Medicamentos/patología , Femenino , Células HaCaT , Humanos , Mediadores de Inflamación/metabolismo , Interleucina-4/metabolismo , Queratinocitos/metabolismo , Queratinocitos/patología , Ratones Endogámicos ICR , Ácido Quínico/análogos & derivados , Ácido Quínico/toxicidad , Rutina/toxicidad , Factor de Necrosis Tumoral alfa/metabolismo
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