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Secondary metabolites changes in germinated barley and its relationship to anti-wrinkle activity.


ABSTRACT: The purpose of this research was to identify metabolite change during barley (Hordeum vulgare) germination and reveal active principles for the anti-wrinkle activity. Barley was germinated with deionized water (DW) and mineral-rich water (MRW) for the comparison of the effect of mineral contents on the metabolites changes during germination. The effects of germinated barley extracts (GBEs) on collagen production and collagenase inhibition were evaluated in vitro using human dermal fibroblasts (HDFs). A pronounced anti-wrinkle activity was observed in the test group treated with the MRW-GBEs. In order to find out the active components related to the anti-wrinkle activity, an orthogonal projection to latent structure-discriminant analysis (OPLS-DA) was performed, using the data from secondary metabolites profiling conducted by UPLC-PDA-ESI-MS. The anti-wrinkle activity of MRW-GBEs was revealed to be associated with the increase of oligomeric compounds of procyanidin and prodelphinidin, indicating that it can be used as an active ingredient for anti-wrinkle agents.

SUBMITTER: Park SC 

PROVIDER: S-EPMC7804254 | biostudies-literature | 2021 Jan

REPOSITORIES: biostudies-literature

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Secondary metabolites changes in germinated barley and its relationship to anti-wrinkle activity.

Park Sang Cheol SC   Wu Qianwen Q   Ko Eun-Yi EY   Baek Ji Hwoon JH   Ryu Jeoungjin J   Kang Seunghyun S   Sung Mi Kyung MK   Cho Ah-Reum AR   Jang Young Pyo YP  

Scientific reports 20210112 1


The purpose of this research was to identify metabolite change during barley (Hordeum vulgare) germination and reveal active principles for the anti-wrinkle activity. Barley was germinated with deionized water (DW) and mineral-rich water (MRW) for the comparison of the effect of mineral contents on the metabolites changes during germination. The effects of germinated barley extracts (GBEs) on collagen production and collagenase inhibition were evaluated in vitro using human dermal fibroblasts (H  ...[more]

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