TY - JOUR
T1 - Liposomes Containing Amaranth Unsaponifiable Matter and Soybean Lunasin Suppress ROS Production in Fibroblasts and Reduced Interleukin Production in Macrophages
AU - Dávila-Ortiz, Gloria
AU - Castañeda-Reyes, Erick Damian
AU - Juárez-Palomo, Carlos Ignacio
AU - Perea-Flores, María de Jesús
AU - Pérez-Pastén-Borja, Ricardo
AU - Márquez-Flores, Yazmín Karina
AU - González de Mejía, Elvira
N1 - Funding Information:
We thank M.C. Aracely Acosta Caudillo for her technical assistance in the study; to the BEIFI program from IPN for the scholarship, SIP Projects 20211113 (Y.K.M.-F.), 20220524 (G.D.-O.), and 20210344 (M.d.J.P.-F.); to Consejo Nacional de Ciencia y Tecnología (CONACyT), México, for the doctoral scholarship to Erick Damián Castañeda Reyes; Ricardo Pérez-Pastén-Borja is grateful to CONACyT for the funding, no. A1-S-25312; and to Secretaría de Investigación y Posgrado del I.P.N. for funding (SIP20221448).
Publisher Copyright:
© 2022 by the authors.
PY - 2022/9
Y1 - 2022/9
N2 - Inflammation is a normal response in defense to agents that may cause damage to the human body. When inflammation becomes chronic, reactive oxygen species (ROS) are produced; which could lead to diseases such as cancer. The aim was to assess liposomes’ antioxidant and anti-inflammatory capacity loaded with amaranth unsaponifiable matter and soybean lunasin (UM + LunLip) in an in vitro model using fibroblasts and macrophages. To evaluate ROS production, fibroblasts CHON-002 ABAP were added to promote ROS production; and the cells were treated with UM + LunLip. For inflammation markers production, lipopolysaccharides (LPS)-stimulated RAW 264.7 and peritoneal macrophages were treated with empty liposomes (EmLip), liposomes loaded with unsaponifiable matter (UMLip), liposomes loaded with lunasin (LunLip), and UM + LunLip. ROS production was significantly decreased by 77% (p < 0.05) when fibroblasts were treated with UM + LunLip at 2 mg lunasin/mL compared with the control treated with ABAP. Treatment with UMLip was the most effective in reducing tumor necrosis factor-α (71–90%) and interleukin-6 (43–55%, p < 0.001). Both liposomes containing unsaponifiable matter (UMLip and UM + LunLip) were more effective than EmLip or LunLip. In conclusion, amaranth unsaponifiable matter-loaded liposomes are effective in decreasing pro-inflammatory cytokine production.
AB - Inflammation is a normal response in defense to agents that may cause damage to the human body. When inflammation becomes chronic, reactive oxygen species (ROS) are produced; which could lead to diseases such as cancer. The aim was to assess liposomes’ antioxidant and anti-inflammatory capacity loaded with amaranth unsaponifiable matter and soybean lunasin (UM + LunLip) in an in vitro model using fibroblasts and macrophages. To evaluate ROS production, fibroblasts CHON-002 ABAP were added to promote ROS production; and the cells were treated with UM + LunLip. For inflammation markers production, lipopolysaccharides (LPS)-stimulated RAW 264.7 and peritoneal macrophages were treated with empty liposomes (EmLip), liposomes loaded with unsaponifiable matter (UMLip), liposomes loaded with lunasin (LunLip), and UM + LunLip. ROS production was significantly decreased by 77% (p < 0.05) when fibroblasts were treated with UM + LunLip at 2 mg lunasin/mL compared with the control treated with ABAP. Treatment with UMLip was the most effective in reducing tumor necrosis factor-α (71–90%) and interleukin-6 (43–55%, p < 0.001). Both liposomes containing unsaponifiable matter (UMLip and UM + LunLip) were more effective than EmLip or LunLip. In conclusion, amaranth unsaponifiable matter-loaded liposomes are effective in decreasing pro-inflammatory cytokine production.
KW - liposomes
KW - inflammation
KW - soybean lunasin
KW - amaranth squalene
KW - ROS-production
KW - tumor necrosis factor-α
KW - interleukin-6
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U2 - 10.3390/ijerph191811678
DO - 10.3390/ijerph191811678
M3 - Article
C2 - 36141952
SN - 1660-4601
VL - 19
JO - International journal of environmental research and public health
JF - International journal of environmental research and public health
IS - 18
M1 - 11678
ER -