PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 34279193-10 2021 In STZ induced diabetes mice models, microglia NLRP3, ASC, and caspase-1 proteins were highly expressed, and serum cytokines IL-1beta, IL6, IL18, and TNFalpha were remarkably increased. Streptozocin 3-6 interleukin 18 Mus musculus 140-144 34685620-8 2021 STZ-induced diabetic cardiomyopathy significantly increased inflammasome formation (TLR4, NLRP3, Nek7, and GBP5), pyroptosis markers (caspase-1, IL-1beta, and IL-18), inflammatory cytokines (IL-6 and TNF-alpha), MMP9, and infiltration of monocytes (CD14), macrophage (iNOS), and dendritic cells (CD11b and CD11c) (p < 0.05). Streptozocin 0-3 interleukin 18 Mus musculus 159-164 32295112-0 2020 The DNA Sensor AIM2 Protects against Streptozotocin-Induced Type 1 Diabetes by Regulating Intestinal Homeostasis via the IL-18 Pathway. Streptozocin 37-51 interleukin 18 Mus musculus 121-126 32295112-7 2020 Mechanistically, the AIM2 inflammasome is activated in vivo, leading to an IL-18 release in the ileum at 15 days after an STZ injection. Streptozocin 122-125 interleukin 18 Mus musculus 75-80 32295112-9 2020 Together, our findings show a regulatory role of AIM2, mediated by IL-18, in shaping gut microbiota and reducing bacterial translocation and proinflammatory response against insulin-producing beta cells, which ultimately results in protection against T1D onset in an STZ-induced diabetes model. Streptozocin 267-270 interleukin 18 Mus musculus 67-72 29435463-4 2017 Results: SAA and IL-18 levels were significantly elevated in diabetic mice (STZ) compared to control (WT) mice, and there was a significant attenuation of inflammation in diabetic NLRP3-KO mice (NLRP3-KO STZ) compared to control mice (p < 0.005). Streptozocin 76-79 interleukin 18 Mus musculus 17-22 12884303-0 2003 Essential pathogenic role of endogenous IL-18 in murine diabetes induced by multiple low doses of streptozotocin. Streptozocin 98-112 interleukin 18 Mus musculus 40-45 12884303-8 2003 We conclude that intact IL-18 function is essential for the full diabetogenic effect of low dose STZ in C57BL/6 mice. Streptozocin 97-100 interleukin 18 Mus musculus 24-29 26923011-8 2016 The STZ treatment also increased the number of Iba-1-positive and CD68-positive microglial cells, astrocytes, and IL-1beta, IL-6, IL-10, and IL-18 levels in the hippocampus, but not in the midbrain or cerebellum. Streptozocin 4-7 interleukin 18 Mus musculus 141-146 22733969-8 2012 Adoptive transfer of unstimulated and IL-18-stimulated NK cells into streptozotocin-treated mice led to a delayed diabetes development and partial disease prevention in the group treated with IL-18-stimulated NK cells. Streptozocin 69-83 interleukin 18 Mus musculus 38-43 22733969-8 2012 Adoptive transfer of unstimulated and IL-18-stimulated NK cells into streptozotocin-treated mice led to a delayed diabetes development and partial disease prevention in the group treated with IL-18-stimulated NK cells. Streptozocin 69-83 interleukin 18 Mus musculus 192-197