Increased Osteoblastic and Osteocytic in Vitro Cell Viability by Yerba Mate (Ilex paraguariensis)
10.11005/jbm.2024.31.2.101
- Author:
Laureana VILLARREAL
1
;
Natasha SANZ
;
Florencia Buiatti FAGALDE
;
Florencia D’ANDREA
;
Mercedes LOMBARTE
;
María J. RICO
;
Viviana R. ROZADOS
;
O. Graciela SCHAROVSKY
;
Lilian I. PLOTKIN
;
Verónica E. DI LORETO
;
Lucas R. BRUN
Author Information
1. Bone Biology Laboratory, School of Medicine, Rosario National University, Rosario, Santa, Argentina
- Publication Type:Original Article
- From:Journal of Bone Metabolism
2024;31(2):101-113
- CountryRepublic of Korea
- Language:English
-
Abstract:
Background:Yerba mate (YM, Ilex paraguariensis) consumption beneficially affects the bones. However, whether YM components exert their effect on bone cells directly remains elusive.
Methods:We evaluated how main YM components affect osteoblastic (MC3T3-E1) and osteocytic (MLO-Y4) cells in vitro when administered separately or in an aqueous extract. MC3T3-E1 and MLO-Y4 cells were exposed to three different experimental conditions: (1) Caffeine, chlorogenic acid, and their combinations; (2) Caffeine, rutin, and their combinations; (3) Aqueous YM extract.
Results:All polyphenol and caffeine concentrations as well as that of their tested combinations significantly increased MC3T3-E1 cell viability from 16.6% to 34.8% compared to the control. In MLO-Y4 cells, the lowest rutin and the two highest caffeine concentrations significantly increased cell viability by 11.9, 14.9, and 13.7%, respectively. While rutin and caffeine combinations tended to increase MLO-Y4 cell viability, different chlorogenic acid and caffeine combinations did not affect it. Finally, the aqueous YM extract significantly increased MLO-Y4, MC3T3-E1, and differentiated MC3T3-E1 cell viability compared to the control without treatment.
Conclusions:YM components (rutin, chlorogenic acid, and caffeine) positively affected bone cells, mainly pre-osteoblast cells. Moreover, the aqueous YM extract significantly increased MLO-Y4, MC3T3-E1, and differentiated MC3T3-E1 cell viabilities indicating an additional relevant nutritional property of YM infusion. Further studies would be required to elucidate the underlying effector mechanism of YM on the bones and its relationship with previously described in vivo positive effects.
