This invention relates to the field of pharmaceuticals, and more particularly to the application of
honeysuckle glycosides or verbenacin in alleviating and / or delaying
renal fibrosis. This invention has discovered that
honeysuckle glycosides can significantly inhibit epithelial-mesenchymal transition, thereby protecting
renal function. More unexpectedly, it has been found that the
combined use of
honeysuckle glycosides and verbenacin significantly enhances the anti-fibrotic effect compared to using either alone, exhibiting a synergistic effect without the serious drawbacks of commonly used clinical drugs. While verbenacin itself possesses certain anti-inflammatory and
antioxidant activity, under the experimental conditions of this invention, the anti-fibrotic effect of verbenacin alone is weaker than that of honeysuckle glycosides; however, when used in combination with honeysuckle glycosides, the latter's anti-fibrotic effect is significantly enhanced, suggesting a complementary or synergistic
molecular mechanism between the two. Therefore, honeysuckle glycosides, used alone or in combination with verbenacin, has a potent and low-
toxicity therapeutic effect on
renal fibrosis. Furthermore, both honeysuckle glycosides and verbenacin are natural compounds, low in
toxicity, and readily accepted by the
human body.