Human neutrophil elastase (HNE), a serine protease with broad target specificity, is the only enzyme responsible for the degradation
of elastin which is an insoluble elastic fibrous protein in animal connective tissue. Biologically, elastase activity significantly
increased with age, which results in a reduced skin elasticity and in the appearance of wrinkles or stretchmarks. In the course
of our screening program for HNE inhibitors from natural source, the MeOH extract of
Ilex paraguariensis leaves showed strong HNE inhibitory effect. Bioassay-guided fractionation led to the isolation of a new pyrrole alkaloid
(
1), along with seventeen known compounds (
2–18) from the MeOH extract of
Ilex paraguariensis leaves, and their chemical structures were elucidated on the basis of spectroscopic analysis. All isolated compounds were
evaluated for HNE inhibitory activity, and the result demonstrated that dicaffeoylquinic acid derivatives (
12,
13,
14,
15 and
16) and flavonoids (
8 and
17) exhibited potent HNE inhibitory activity with IC
50 values ranging from 1.4 to 7.3 µM.
Key words Human neutrophil elastase -
Ilex paraguariensis
- Dicaffeoylquinic acid derivatives - Pyrrolezanthine-6-methyl ether