scholarly journals Inhibition of Mushroom Tyrosinase and Melanogenesis B16 Mouse Melanoma Cells by Components Isolated from Curcuma longa

2008 ◽  
Vol 3 (10) ◽  
pp. 1934578X0800301 ◽  
Author(s):  
Jeong Ah Kim ◽  
Jong Keun Son ◽  
Hyun Wook Chang ◽  
Yurngdong Jahng ◽  
Youngsoo Kim ◽  
...  

The methanol extract of the rhizomes of Curcuma longa was found to inhibit tyrosinase activity. After partition, various column chromatographic and preparative HPLC procedures were used for bioassay guided isolation from the active ethyl acetate-soluble fraction. Various spectroscopic (1D-, 2D-NMR) and mass spectrometric techniques, and Mosher's esterification were applied to elucidate the structures of the isolated compounds. The isolates were tested using an in vitro mushroom tyrosinase assay. Inhibition of melanin formation by the active compounds was further evaluated using B16 mouse melanoma cells. Eleven compounds (1 – 11) were isolated from the rhizomes of C. longa by bioassay guided fractionation. The configuration at the C-4 position of 4-hydroxy-1,3(15),10-bisabolatrien-9-one (11) was confirmed by Mosher's method. Of the isolates, curcuminoids 5 - 7 showed potent inhibitory activity in the tyrosinase assay. Melanin formation of the active compounds in the B16 mouse melanoma cells corresponded with the tyrosinase inhibitory activity. The findings support the view that either curcuminoids or the extract of C. longa rhizomes containing them may be useful for the treatment of hyperpigmentation.

2007 ◽  
Vol 56 (12) ◽  
pp. 645-648 ◽  
Author(s):  
Mikio Kinoshita ◽  
Naofumi Hori ◽  
Kazuhiko Aida ◽  
Tatsuya Sugawara ◽  
Masao Ohnishi

2011 ◽  
Vol 6 (9) ◽  
pp. 1934578X1100600 ◽  
Author(s):  
Enos Tangke Arung ◽  
Kuniyoshi Shimizu ◽  
Ryuichiro Kondo

Artocarpus plants have been a focus of constant attention due to the potential for skin whitening agents. In the in vitro experiment, compounds from the Artocarpus plants, such as artocarpanone, norartocarpetin, artocarpesin, artogomezianol, andalasin, artocarbene, and chlorophorin showed tyrosinase inhibitory activity. Structure-activity investigations revealed that the 4-substituted resorcinol moiety in these compounds was responsible for their potent inhibitory activities on tyrosinase. In the in vitro assay, using B16 melanoma cells, the prenylated polyphenols isolated from Artocarpus plants, such as artocarpin, cudraflavone C, 6-prenylapigenin, kuwanon C, norartocarpin, albanin A, cudraflavone B, and brosimone I showed potent inhibitory activity on melanin formation. Structure-activity investigations revealed that the introduction of an isoprenoid moiety to a non-isoprenoid-substituted polyphenol enhanced the inhibitory activity of melanin production in B16 melanoma cells. In the in vivo investigation, the extract of the wood of Artocarpus incisus and a representative isolated compound from it, artocarpin had a lightening effect on the skin of guinea pigs’ backs. Other in vivo experiments using human volunteers have shown that water extract of Artocarpus lakoocha reduced the melanin formation in the skin of volunteers. These results indicate that the extracts of Artocarpus plants are potential sources for skin whitening agents.


2015 ◽  
Vol 14 (7) ◽  
pp. 1582-1590 ◽  
Author(s):  
Yun Xia ◽  
Xian-Yi Cai ◽  
Ji-Quan Fan ◽  
Li-Ling Zhang ◽  
Jing-Hua Ren ◽  
...  

2004 ◽  
Vol 12 (20) ◽  
pp. 5349-5354 ◽  
Author(s):  
Isao Kubo ◽  
Ken-ichi Nihei ◽  
Kazuo Tsujimoto

2021 ◽  
Vol 41 (12) ◽  
pp. 6113-6121
Author(s):  
HIRONORI USHIJIMA ◽  
RINA MONZAKI ◽  
ARISA ONODERA

Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 1066
Author(s):  
Ali Zari ◽  
Hajer Alfarteesh ◽  
Carly Buckner ◽  
Robert Lafrenie

Uncaria tomentosa is a medicinal plant native to Peru that has been traditionally used in the treatment of various inflammatory disorders. In this study, the effectiveness of U. tomentosa as an anti-cancer agent was assessed using the growth and survival of B16-BL6 mouse melanoma cells. B16-BL6 cell cultures treated with both ethanol and phosphate-buffered saline (PBS) extracts of U. tomentosa displayed up to 80% lower levels of growth and increased apoptosis compared to vehicle controls. Treatment with ethanolic extracts of Uncaria tomentosa were much more effective than treatment with aqueous extracts. U. tomentosa was also shown to inhibit B16-BL6 cell growth in C57/bl mice in vivo. Mice injected with both the ethanolic and aqueous extracts of U. tomentosa showed a 59 ± 13% decrease in B16-BL6 tumour weight and a 40 ± 9% decrease in tumour size. Histochemical analysis of the B16-BL6 tumours showed a strong reduction in the Ki-67 cell proliferation marker in U. tomentosa-treated mice and a small, but insignificant increase in terminal transferase dUTP nick labelling (TUNEL) staining. Furthermore, U. tomentosa extracts reduced angiogenic markers and reduced the infiltration of T cells into the tumours. Collectively, the results in this study concluded that U. tomentosa has potent anti-cancer activity that significantly inhibited cancer cells in vitro and in vivo.


2007 ◽  
Vol 17 (1) ◽  
pp. 17-30 ◽  
Author(s):  
Matthias Oppitz ◽  
Christian Busch ◽  
Gernot Schriek ◽  
Marco Metzger ◽  
Lothar Just ◽  
...  

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