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1.
J Med Chem ; 63(5): 2282-2291, 2020 03 12.
Artículo en Inglés | MEDLINE | ID: mdl-31418565

RESUMEN

Cancer immunotherapy has gained increasing attention due to its potential specificity and lack of adverse side effects when compared to more traditional modes of treatment. Toll-like receptor 2 (TLR2) agonists are lipopeptides possessing the S-[2,3-bis(palmitoyloxy)propyl]-l-cysteine (Pam2Cys) motif and exhibit potent immunostimulatory effects. These agonists offer a means of providing "danger signals" in order to activate the immune system toward tumor antigens. Thus, the development of TLR2 agonists is attractive in the search of potential immunostimulants for cancer. Existing SAR studies of Pam2Cys with TLR2 indicate that the structural requirements for activity are, for the most part, very intolerable. We have investigated the importance of stereochemistry, the effect of N-terminal acylation, and homologation between the two ester functionalities in Pam2Cys-conjugated lipopeptides on TLR2 activity. The R diastereomer is significantly more potent than the S diastereomer and N-terminal modification generally lowers TLR2 activity. Most notably, homologation gives rise to analogues which are comparatively active to the native Pam2Cys containing constructs.


Asunto(s)
Adyuvantes Inmunológicos/química , Adyuvantes Inmunológicos/farmacología , Lipopéptidos/química , Lipopéptidos/farmacología , Receptor Toll-Like 2/agonistas , Adyuvantes Inmunológicos/síntesis química , Vacunas contra el Cáncer/farmacología , Cisteína/análogos & derivados , Cisteína/síntesis química , Cisteína/farmacología , Humanos , Lipopéptidos/síntesis química , Neoplasias/prevención & control , Estereoisomerismo , Receptor Toll-Like 2/metabolismo
2.
Br J Pharmacol ; 175(9): 1439-1450, 2018 05.
Artículo en Inglés | MEDLINE | ID: mdl-29315511

RESUMEN

BACKGROUND AND PURPOSE: Increasing energy expenditure through adipocyte thermogenesis is generally accepted as a promising strategy to mitigate obesity and its related diseases. However, few clinically effective and safe agents are known to promote adipocyte thermogenesis. In this study, 20 traditional Chinese herbal medicines were screened to examine whether they induced adipocyte thermogenesis. EXPERIMENTAL APPROACH: The effects of Chinese herbal medicines or components isolated from extracts of A. membranaceus, on adipocyte thermogenesis were analysed by assessing expression of uncoupling protein 1 (UCP1) by qPCR. Eight-week-old C57BL6/J male mice were fed a high-fat diet for 8 weeks and then randomized to two groups treated with vehicle or formononetin for another 8 weeks. Glucose tolerance tests and staining of adipose tissue with haematoxylin and eosin were carried out. Whole-body oxygen consumption was measured with an open-circuit indirect calorimetry system. KEY RESULTS: Extracts of A. membranaceus increased expression of Ucp1 in primary cultures of mouse adipocytes. Formononetin was the only known component of A. membranaceus extracts to increase adipocyte Ucp1 expression. Diet-induced obese mice treated with formononetin gained less weight and showed higher energy expenditure than untreated mice. In addition, formononetin binds directly with PPARγ. CONCLUSIONS AND IMPLICATION: Taken together, our study demonstrates that the Chinese herbal medicine from A. membranaceus and its constituent formononetin have the potential to reduce obesity and associated metabolic disorders. Our results suggest that formononetin regulates adipocyte thermogenesis as a non-classical PPARγ agonist.


Asunto(s)
Adipocitos/efectos de los fármacos , Astragalus propinquus/química , Isoflavonas/aislamiento & purificación , Isoflavonas/farmacología , PPAR gamma/metabolismo , Termogénesis/efectos de los fármacos , Adipocitos/metabolismo , Animales , Peso Corporal/efectos de los fármacos , Dieta Alta en Grasa , Relación Dosis-Respuesta a Droga , Medicamentos Herbarios Chinos/farmacología , Metabolismo Energético/efectos de los fármacos , Prueba de Tolerancia a la Glucosa , Masculino , Ratones , Obesidad/inducido químicamente , Obesidad/prevención & control , Consumo de Oxígeno/efectos de los fármacos , PPAR gamma/fisiología , Extractos Vegetales/química , Extractos Vegetales/farmacología , Cultivo Primario de Células , ARN Interferente Pequeño/farmacología , Termogénesis/fisiología , Proteína Desacopladora 1/biosíntesis
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