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1.
Molecules ; 29(11)2024 May 24.
Article in English | MEDLINE | ID: mdl-38893349

ABSTRACT

This study aimed to isolate and purify resveratrol and oxyresveratrol from the heartwoods of Maclura cochinchinensis, and to evaluate their inhibitory effects on melanogenesis in B16F10 murine melanoma cells. A methanol maceration process yielded a crude extract comprising 24.86% of the initial mass, which was subsequently analyzed through HPTLC, HPLC, and LC-MS/MS. These analyses revealed the presence of resveratrol and oxyresveratrol at concentrations of 4.32 mg/g and 33.6 mg/g in the extract, respectively. Initial purification employing food-grade silica gel column chromatography separated the extract into two fractions: FA, exhibiting potent inhibition of both tyrosinase activity and melanogenesis, and FM, showing no such inhibitory activity. Further purification processes led to the isolation of fractions Y11 and Gn12 with enhanced concentrations of resveratrol (94.9 and 110.21 mg/g, respectively) and fractions Gn15 and Gn16 with elevated levels of oxyresveratrol (321.93 and 274.59 mg/g, respectively), all of which significantly reduced melanin synthesis. These outcomes affirm the substantial presence of resveratrol and oxyresveratrol in the heartwood of M. cochinchinensis, indicating their promising role as natural agents for skin lightening.


Subject(s)
Melanins , Melanoma, Experimental , Plant Extracts , Resveratrol , Stilbenes , Resveratrol/pharmacology , Resveratrol/chemistry , Plant Extracts/pharmacology , Plant Extracts/chemistry , Animals , Mice , Melanins/biosynthesis , Stilbenes/pharmacology , Stilbenes/chemistry , Melanoma, Experimental/metabolism , Melanoma, Experimental/pathology , Cell Line, Tumor , Monophenol Monooxygenase/antagonists & inhibitors , Monophenol Monooxygenase/metabolism , Chromatography, High Pressure Liquid , Tandem Mass Spectrometry , Melanogenesis
2.
Biologicals ; 64: 83-95, 2020 Mar.
Article in English | MEDLINE | ID: mdl-32089431

ABSTRACT

Rabies is a major neglected zoonotic disease and causes a substantial burden in the Asian region. Currently, Pacific Oceania is free of rabies but enzootic areas throughout southeast Asia represent a major risk of disease introduction to this region. On September 25-26, 2019, researchers, government officials and related stakeholders met at an IABS conference in Bangkok, Thailand to engage on the topic of human rabies mediated by dogs. The objective of the meeting was focused upon snowballing efforts towards achieving substantial progress in rabies prevention, control and elimination within Asia by 2030, and thereby to safeguard the Pacific region. Individual sessions focused upon domestic animal, wildlife and human vaccination; the production and evaluation of quality, safety and efficacy of existing rabies biologics; and the future development of new products. Participants reviewed the progress to date in eliminating canine rabies by mass vaccination, described supportive methods to parenteral administration by oral vaccine application, considered updated global and local approaches at human prophylaxis and discussed the considerable challenges ahead. Such opportunities provide continuous engagement on disease management among professionals at a trans-disciplinary level and promote new applied research collaborations in a modern One Health context.


Subject(s)
Dog Diseases , Rabies Vaccines/therapeutic use , Rabies , Zoonoses , Animals , Congresses as Topic , Dog Diseases/epidemiology , Dog Diseases/prevention & control , Dogs , Humans , Rabies/epidemiology , Rabies/prevention & control , Thailand , Zoonoses/epidemiology , Zoonoses/prevention & control
3.
Molecules ; 23(6)2018 06 09.
Article in English | MEDLINE | ID: mdl-29890751

ABSTRACT

Twenty-seven flavonoids isolated from Dalbergia parviflora with vast structural diversity were screened for inhibitory activity against mushroom and murine tyrosinases using l-DOPA as the substrate. Among the flavonoids tested, only four­khrinone (5), cajanin (9), (3RS)-3'-hydroxy-8-methoxy vestitol (21), and (6aR,11aR)-3,8-dihydroxy-9-methoxy pterocarpan (27)­reacted with mushroom tyrosinase, with IC50 values of 54.0, 67.9, 67.8, and 16.7 µM, respectively, and only compound 27 showed inhibitory activity against murine tyrosinase. With cell-based assays, only compounds 9 and 27 effectively inhibited melanogenesis in B16-F10 melanoma cells (by 34% and 59%, respectively), at a concentration of 15 µM, without being significantly toxic to the cells. However, the crude extract of D. parviflora and some of the flavonoid constituents appeared to increase melanin production in B16-F10 cells, suggesting that there are flavonoids with both inhibitory and stimulatory melanogenesis in the crude extract. Studies on the correlation between the enzyme-based and cell-based assays showed that only the flavonoids with IC50 values below 50 µM against mushroom tyrosinase could inhibit the mammalian tyrosinase, and thus, reduce melanogenesis in B16-F10. Flavonoids with the IC50 values greater than 50 µM, on the other hand, could not inhibit the mammalian tyrosinase, and had either no effect or enhancement of melanogenesis. In conclusion, the tyrosinase enzyme from mushroom is not as selective as the one from mammalian source for the enzyme-based melanogenesis inhibitory screening, and the mammalian cell-based assay appears to be a more reliable model for screening than the enzyme-based one.


Subject(s)
Agaricales/enzymology , Flavonoids/pharmacology , Melanins/biosynthesis , Melanocytes/drug effects , Monophenol Monooxygenase/antagonists & inhibitors , Melanocytes/metabolism
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