Matches in SemOpenAlex for { <https://semopenalex.org/work/W1930477314> ?p ?o ?g. }
- W1930477314 abstract "Type 1 diabetes mellitus (T1D) is a chronic autoimmune disease caused by the selective destruction of pancreatic β cells, followed by hyperglycemia, oxidative stress and the subsequent extensive impairment of immune cell functions, a phenomenon responsible for the development of chronic diabetic complications. Propolis, a natural bee product that is extensively used in foods and beverages, significantly benefits human health. Specifically, propolis exerts antioxidant, anti-inflammatory and analgesic effects that may improve diabetic complications. To further elucidate the potential benefits of propolis, the present study investigated the effect of dietary supplementation with propolis on the plasma cytokine profiles, free radical levels, lipid profile and lymphocyte proliferation and chemotaxis in a streptozotocin (STZ)-induced type I diabetic mouse model. Thirty male mice were equally distributed into 3 experimental groups: group 1, non-diabetic control mice; group 2, diabetic mice; and group 3, diabetic mice supplemented daily with an ethanol-soluble derivative of propolis (100 mg/kg body weight) for 1 month. First, the induction of diabetes in mice was associated with hyperglycemia and significant decreases in the insulin level and the lymphocyte count. In this context, diabetic mice exhibited severe diabetic complications, as demonstrated by a significant decrease in the levels of IL-2, IL-4 and IL-7, prolonged elevation of the levels of pro-inflammatory cytokines (IL-1β, IL-6 and TNF-α) and reactive oxygen species (ROS) and altered lipid profiles compared with control non-diabetic mice. Moreover, antigen stimulation of B and T lymphocytes markedly reduced the proliferative capacity and chemotaxis of these cells towards CCL21 and CXCL12 in diabetic mice compared with control mice. Interestingly, compared with diabetes induction alone, treatment of diabetic mice with propolis significantly restored the plasma cytokine and ROS levels and the lipid profile to nearly normal levels. Most importantly, compared with untreated diabetic mice, diabetic mice treated with propolis exhibited significantly enhanced lymphocyte proliferation and chemotaxis towards CCL21 and CXCL12. Our findings reveal the potential immuno-modulatory effects of propolis, which acts as a natural antioxidant to enhance the function of immune cells during diabetes." @default.
- W1930477314 created "2016-06-24" @default.
- W1930477314 creator A5014167283 @default.
- W1930477314 creator A5026693289 @default.
- W1930477314 creator A5031831253 @default.
- W1930477314 creator A5051676321 @default.
- W1930477314 creator A5058870203 @default.
- W1930477314 creator A5062652662 @default.
- W1930477314 creator A5074867644 @default.
- W1930477314 date "2015-09-15" @default.
- W1930477314 modified "2023-10-10" @default.
- W1930477314 title "Oral supplementation of diabetic mice with propolis restores the proliferation capacity and chemotaxis of B and T lymphocytes towards CCL21 and CXCL12 by modulating the lipid profile, the pro-inflammatory cytokine levels and oxidative stress" @default.
- W1930477314 cites W1491280754 @default.
- W1930477314 cites W1530509485 @default.
- W1930477314 cites W1564463072 @default.
- W1930477314 cites W1601504908 @default.
- W1930477314 cites W1605373480 @default.
- W1930477314 cites W1638707930 @default.
- W1930477314 cites W1832886183 @default.
- W1930477314 cites W1904467505 @default.
- W1930477314 cites W1931315964 @default.
- W1930477314 cites W1949832432 @default.
- W1930477314 cites W1963575613 @default.
- W1930477314 cites W1963628169 @default.
- W1930477314 cites W1965792890 @default.
- W1930477314 cites W1971674645 @default.
- W1930477314 cites W1980097080 @default.
- W1930477314 cites W1981411216 @default.
- W1930477314 cites W1983346506 @default.
- W1930477314 cites W1985330687 @default.
- W1930477314 cites W1987052041 @default.
- W1930477314 cites W1992343847 @default.
- W1930477314 cites W1994956984 @default.
- W1930477314 cites W1995311442 @default.
- W1930477314 cites W1998221258 @default.
- W1930477314 cites W2001709426 @default.
- W1930477314 cites W2005225225 @default.
- W1930477314 cites W2008833979 @default.
- W1930477314 cites W2017812837 @default.
- W1930477314 cites W2022636346 @default.
- W1930477314 cites W2038452157 @default.
- W1930477314 cites W2040722201 @default.
- W1930477314 cites W2042384977 @default.
- W1930477314 cites W2044524894 @default.
- W1930477314 cites W2047368370 @default.
- W1930477314 cites W2053356284 @default.
- W1930477314 cites W2067539745 @default.
- W1930477314 cites W2069797199 @default.
- W1930477314 cites W2073102935 @default.
- W1930477314 cites W2073973554 @default.
- W1930477314 cites W2077453377 @default.
- W1930477314 cites W2080400596 @default.
- W1930477314 cites W2085293124 @default.
- W1930477314 cites W2087470941 @default.
- W1930477314 cites W2093300567 @default.
- W1930477314 cites W2093606512 @default.
- W1930477314 cites W2095231567 @default.
- W1930477314 cites W2106049963 @default.
- W1930477314 cites W2106243784 @default.
- W1930477314 cites W2108306062 @default.
- W1930477314 cites W2111536891 @default.
- W1930477314 cites W2113450829 @default.
- W1930477314 cites W2113936086 @default.
- W1930477314 cites W2120472250 @default.
- W1930477314 cites W2126496496 @default.
- W1930477314 cites W2128049871 @default.
- W1930477314 cites W2129860342 @default.
- W1930477314 cites W2130293973 @default.
- W1930477314 cites W2132984693 @default.
- W1930477314 cites W2150295492 @default.
- W1930477314 cites W2152656461 @default.
- W1930477314 cites W2153979257 @default.
- W1930477314 cites W2157719263 @default.
- W1930477314 cites W2168846495 @default.
- W1930477314 cites W2174528613 @default.
- W1930477314 cites W2199624279 @default.
- W1930477314 cites W2317145780 @default.
- W1930477314 cites W2319525885 @default.
- W1930477314 cites W2319961023 @default.
- W1930477314 cites W2411826498 @default.
- W1930477314 cites W2471605942 @default.
- W1930477314 cites W4213000396 @default.
- W1930477314 doi "https://doi.org/10.1186/s12865-015-0117-9" @default.
- W1930477314 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4570673" @default.
- W1930477314 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26370805" @default.
- W1930477314 hasPublicationYear "2015" @default.
- W1930477314 type Work @default.
- W1930477314 sameAs 1930477314 @default.
- W1930477314 citedByCount "39" @default.
- W1930477314 countsByYear W19304773142015 @default.
- W1930477314 countsByYear W19304773142016 @default.
- W1930477314 countsByYear W19304773142017 @default.
- W1930477314 countsByYear W19304773142018 @default.
- W1930477314 countsByYear W19304773142019 @default.
- W1930477314 countsByYear W19304773142020 @default.
- W1930477314 countsByYear W19304773142021 @default.
- W1930477314 countsByYear W19304773142022 @default.
- W1930477314 countsByYear W19304773142023 @default.
- W1930477314 crossrefType "journal-article" @default.
- W1930477314 hasAuthorship W1930477314A5014167283 @default.