Open AccessIdentification of natural products and their derivatives as promising inhibitors of protein glycation with non-toxic nature against mouse fibroblast 3T3 cells
Author(s) -
Ghulam Abbas,
Ahmed Suliman Al-Harrasi,
Hidayat Hussain,
Samina A. Sattar,
M. Iqbal Choudhary
Publication year - 2017
Publication title -
international journal of phytomedicine
Language(s) - English
Resource type - Journals
ISSN - 0975-0185
DOI - 10.5138/09750185.1924
Subject(s) - chemistry , gossypol , in vitro , glycation , microbiology and biotechnology , biochemistry , biology , receptor
This study was performed to identify new inhibitors of protein glycation in vitro . Protein glycation is one of the major causes of late diabetic complications. In this study, terpenoids and alkaloids, isolated from different medicinal plants, along with their derivatives, were evaluated for their antiglycation activity in vitro, while MTT assay on mouse fibroblast 3T3 cells was used to assess their potential cytotoxicity. Among the tested compounds, gossypol (2,2′- bis -(formyl-1,6,7-trihydroxy-5-isopropyl-3-methylnaphthalene) ( 1 ), isolated from Gossypium herbaceum, and its derivatives, gossypol acetic acid ( 2 ), gossypolidene- 4-aminoantipyrine ( 4 ), and gazolidone ( 6 ), showed a potent antiglycation activity (IC 50 < 16 µ M), while gossypolidene-4-aminoantipyrine ( 5 ) showed a significant antiglycation activity with IC 50 value 82.934±2.924 µ M, in BSA-fluorescence assay. Alkaloid, noscapine (3S)-6,7-Dimethoxy-3-[(5R)-4-methoxy-6-methyl-5,6,7,8-tetrahy-dro-1,3-dioxolo[4,5-g]isoquinolin-5-yl] isobenzofuran-1(3 H )-one ( 7 ), isolated from Papaver somniferum, N -nitrosoaphyllinic acid ( 9 ), a derivative of alkaloid aphylline , and 2 H -quinolizine, octahydro salt ( 11 ), a salt of alkaloid lupinine, exhibited significant inhibition activity with IC 50 values 152.662±5.432, 393.758 ±4.001 µM and 110.203±4.816µM, respectively. Similarly, compounds gossypolidene thiocarbamide ( 3 ), deoxypeganine hydrochloride ( 8 ) , lupinine ( 10 ) and cytisine ( 12 ) showed moderate inhibition with IC 50 values of 401.865 ±18.450, 863.322 ±6.415, 712.176±7.745, and 728.462±2.331 µM, respectively. The results were compared with the standard antiglycation agent, rutin ( 13 ) (IC 50 =98.012±2.030 µM). Cellular cytotoxicity assay showed only gossypol acetic acid ( 2 ) and gossypolidene thiocarbamide ( 3 ) as somewhat toxic to 3T3 (mouse fibroblast) cells with IC 50 values 2.07 ±0.61 and 5.00 ±1.89 µM, respectively. Cycloheximide was used as a standard in this assay with IC 50 value 0.3 ± 0.089 μM