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1.
Artículo en Chino | WPRIM | ID: wpr-775384

RESUMEN

Ferroptosis is a new form of regulated cell death which is different from apoptosis, necrosis and autophagy, and results from iron-dependent lipidperoxide accumulation. Now, it is found that ferroptosis is involved in multiple physiological and pathological processes, such as cancer, arteriosclerosis, neurodegenerative diseases, diabetes, antiviral immune response, acute renal failure, hepatic and heart ischemia/reperfusion injury. On the one hand, it could be found the appropriate drugs to promote ferroptosis to clear cancer cells and virus infected cells, etc. On the other hand, we could inhibit ferroptosis to protect healthy cells. China has a wealth of traditional Chinese medicine resources. Chinese medicine contains a variety of active ingredients that regulate ferroptosis. Here, this paper reported the research of ferroptosis pathway, targets of its inducers and inhibitors that have been discovered, and the regulatory effects of the discovered Chinese herbs and its active ingredients on ferroptosis to help clinical and scientific research.


Asunto(s)
Humanos , Apoptosis , China , Medicamentos Herbarios Chinos , Farmacología , Hierro , Materia Medica , Farmacología
2.
Acta Pharmaceutica Sinica ; (12): 798-802, 2007.
Artículo en Chino | WPRIM | ID: wpr-268576

RESUMEN

To observe the effects of phenylallyl compounds on prostaglandin E2 (PGE2) release in mouse cerebral microvascular endothelial cells (bEnd. 3) stimulated by IL-1beta, and to analyze their structure-activity relationship. Different concentrations of phenylallyl compounds were added separately, and the content of PGE2 induced by IL-1beta in the culture media was measured by ELISA assay. The 50% inhibitory concentration (IC50) of PGE2 was calculated. Studies showed that phenylallyl compounds could affect the PGE2 release differently in bEnd. 3 cells induced by IL-1beta. Close relationships were shown between the inhibitory activities and the location and number of the substituent groups. In conclusion, phenylallyl compounds exhibited inhibitory activities at different extent on PGE2 release in bEnd. 3 cells stimulated by IL-1beta and presented certain structure-activity relationship.


Asunto(s)
Animales , Ratones , Acroleína , Farmacología , Encéfalo , Células Cultivadas , Cinamatos , Farmacología , Dinoprostona , Secreciones Corporales , Medicamentos Herbarios Chinos , Química , Células Endoteliales , Biología Celular , Metabolismo , Concentración 50 Inhibidora , Interleucina-1beta , Farmacología , Microvasos , Biología Celular , Propanoles , Farmacología , Relación Estructura-Actividad
3.
Artículo en Chino | WPRIM | ID: wpr-245980

RESUMEN

<p><b>OBJECTIVE</b>To investigate the influences of Shensu Yin to RAW 264.7 on the expression of TLR3, TLR4 and the factors of the downstream in RAW 264. 7 cells.</p><p><b>METHOD</b>RAW 264.7 cell line was stimulated with Lipopolysaccharide and POLY I: C, respectively, and treated with the drug serum of Shensuyin simultaneously. 24 hours later, collected the supernatant and measured the inflammatory factors TNF-alpha and IFN-beta, extracted mRNA and measured the expression of TLR3, TLR4 and other correlated indexes of the downstream, analyzed and evaluated Shensu Yin's substance basis of pharmacodynamic actions.</p><p><b>RESULT</b>Shensu Yin drug serum depressed the expression of TLR4, MyD88, TRAF-6, TRAM and TRIF mRNA, as a result, it decreased the amount of TNF-alpha and IFN-beta.</p><p><b>CONCLUSION</b>Depressing the expression of TLR3, MyD88, TRAM and TRIF mRNA may be the elementary basis of Shensu Yin to play heat-clearing and detoxicating effect.</p>


Asunto(s)
Animales , Masculino , Ratones , Ratas , Proteínas Adaptadoras del Transporte Vesicular , Genética , Línea Celular , Combinación de Medicamentos , Medicamentos Herbarios Chinos , Farmacología , Interferón beta , Secreciones Corporales , Lipopolisacáridos , Farmacología , Macrófagos , Biología Celular , Metabolismo , Factor 88 de Diferenciación Mieloide , Genética , Plantas Medicinales , Química , Poli I-C , Farmacología , ARN Mensajero , Genética , Distribución Aleatoria , Ratas Sprague-Dawley , Receptores de Interleucina , Genética , Transducción de Señal , Receptor Toll-Like 3 , Genética , Receptor Toll-Like 4 , Genética , Factor de Necrosis Tumoral alfa , Secreciones Corporales
4.
Artículo en Chino | WPRIM | ID: wpr-351004

RESUMEN

<p><b>OBJECTIVE</b>To investigate the changes of the activity of both protein kinase A and C and the mechanisms of antipyretic action of Guizhi decoction.</p><p><b>METHOD</b>The fever responses were observed after combination injection of H-89 (a selective inhibitor of PKA) and calphostin C (a selective inhibitor of PKC), and oral pretreatment of Guizhi decoction in fever rats induced by an intra-cerebroventricular (icv) injection of an EP3 agonist, and both PKA and PKC activity in hypothalamus were measured in rats pretreated with Guizhi decoction and vehicle using isotopic tracing assay.</p><p><b>RESULT</b>The rise in rat body temperature was inhibited by H-89, Calphostin C, and Guizhi decoction, moreover, pretreatment with Guizhi decoction reduced PKA activity obviously. PKC activity in model rats exhibited a tendency to drop compared with that of control group, Oral administration of Guizhi decoction in large dose inhibited the response significantly, while the low dose of Guzhi decoction has no effect on PKC.</p><p><b>CONCLUSION</b>Both PKA and PKC may participate in the mechanism of fever induction by EP3 agonist. The decrease of PKA and PKC may contribute to the antipyretic action of Guizhi decoction, some isoenzyme of PKC may play a role in the fever production.</p>


Asunto(s)
Animales , Masculino , Ratas , Analgésicos no Narcóticos , Farmacología , Cinnamomum aromaticum , Química , Proteínas Quinasas Dependientes de AMP Cíclico , Metabolismo , Dinoprostona , Relación Dosis-Respuesta a Droga , Combinación de Medicamentos , Medicamentos Herbarios Chinos , Farmacología , Fiebre , Hipotálamo , Plantas Medicinales , Química , Proteína Quinasa C , Metabolismo , Distribución Aleatoria , Ratas Wistar , Receptores de Prostaglandina E , Subtipo EP3 de Receptores de Prostaglandina E
5.
Artículo en Chino | WPRIM | ID: wpr-293727

RESUMEN

<p><b>OBJECTIVE</b>To investigate the effect of Guizhi Tang and its active components on the fever induced by EP3 receptor agonist sulprostone in rats.</p><p><b>METHOD</b>The rise in body temperature evoked by a LCV(lateral cerebroventricle)-injection of sulprostone was compared with that of sulprostone induced-fever rats pretreated with Guizgi Tang and its active compounds, cinnamaldehyde, cinnamic acid and total glucosides of paeony.</p><p><b>RESULT</b>Pretreatments with Guizhi Tang and cinnamaldehyde inhibited the rise in body temperature induced by sulprostone, while cinnamic acid tended to augment the fever. The sulprostone-induced fever was blocked by an ip pretreatment of total glucosides of paeony even below the basement.</p><p><b>CONCLUSION</b>Present data suggest that interruption with the down-stream events of EP3 receptor may contribute to the antipyretic action of Guizhi Tang, cinnamaldehyde and the total glucosides of paeony, while cinnamic acid may have no such effect.</p>


Asunto(s)
Animales , Masculino , Ratas , Acroleína , Farmacología , Analgésicos no Narcóticos , Farmacología , Temperatura Corporal , Cinamatos , Farmacología , Dinoprostona , Combinación de Medicamentos , Medicamentos Herbarios Chinos , Farmacología , Fiebre , Glucósidos , Farmacología , Paeonia , Química , Plantas Medicinales , Química , Ratas Wistar , Receptores de Prostaglandina E , Subtipo EP3 de Receptores de Prostaglandina E
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