PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 30254425-8 2018 Additionally, the expression of IL-1beta, IL-6, monocyte chemotactic protein-1, macrophage inflammatory protein-1alpha and TGF-beta were significantly decreased by tacrolimus. Tacrolimus 164-174 interleukin 1 beta Rattus norvegicus 32-40 30713033-10 2019 RESULTS: In rats pre-treated with FK506, the levels of transaminases, TNF-alpha and IL-1beta were reduced significantly and also liver damage was dramatically mitigated compared to those without FK506 pre-treatment. Tacrolimus 34-39 interleukin 1 beta Rattus norvegicus 84-92 15047987-4 2004 CsA (at concentrations of 10-50 microM), FK506 (at all used concentrations) and rapamycin (in dose-dependent manner) significantly attenuated IL-1beta release after 24 h exposure to ischemic conditions. Tacrolimus 41-46 interleukin 1 beta Rattus norvegicus 142-150 17367747-5 2007 More specifically, Tacrolimus suppressed the expression of serum interleukin (IL-1beta), tumour necrosis factor (TNF-alpha), IL-6, airpouch exudate PGE(2) and leukocytosis usually observed after the induction of periodontitis. Tacrolimus 19-29 interleukin 1 beta Rattus norvegicus 78-86 15390105-8 2005 In FK506-treated rats, a significant reduction of IL-1beta, IL-6, and TNF-alpha expression was observed 12 h after reperfusion. Tacrolimus 3-8 interleukin 1 beta Rattus norvegicus 50-58 15390105-9 2005 FK506 neuroprotection was associated with a significant downregulation of IL-1beta expression in astrocytes and microglia in the injured side. Tacrolimus 0-5 interleukin 1 beta Rattus norvegicus 74-82 15390105-10 2005 FK506 selectively decreased the levels of TNF-alpha, and IL-1beta mRNAs in astrocytes in vitro, with no effect on transforming growth factor-beta 1 (TGF-beta1) and IL-6 expression. Tacrolimus 0-5 interleukin 1 beta Rattus norvegicus 57-65 27572744-9 2017 Moreover, the results in hypoxia-treated primary spinal cord microglia confirmed the effect of FK-506 on TNF-a, IL-1b, and IL-6 expression and NF-kappaB activation. Tacrolimus 95-101 interleukin 1 beta Rattus norvegicus 112-117 22806180-5 2012 While both drugs efficiently reduced the expression of iNOS and the release of nitric oxide, only FK506 strongly inhibited the expression of Cox-2 and secretion of the mature form of IL-1beta. Tacrolimus 98-103 interleukin 1 beta Rattus norvegicus 183-191 19815232-7 2011 Real-time RT-PCR and Western blotting showed that pretreatment with low-dose FK506 partially inhibited AIF-1 activation as well as its inducers (IFN-gamma and IL-1beta) in these three models. Tacrolimus 77-82 interleukin 1 beta Rattus norvegicus 159-167 20402659-10 2010 Treatment with all three drugs (tacrolimus, somatostatin and glucocorticoids) resulted in a significant decrease of serum amylase, lung edema, and serum TNF-alpha and IL-1beta levels. Tacrolimus 32-42 interleukin 1 beta Rattus norvegicus 167-175 17367747-6 2007 Tacrolimus treatment in periodontitis-induced rats conferred protection against the inflammation-induced tissue and bone loss associated with periodontitis, through a mechanism involving IL-1beta, TNF-alpha and IL-6. Tacrolimus 0-10 interleukin 1 beta Rattus norvegicus 187-195 17612778-8 2007 This study shows that conversion from CsA to tacrolimus therapy leads to a reversal of the CsA-induced bone loss, which can probably be mediated by downregulation of IL-1beta, IL-6, and TNF-alpha production. Tacrolimus 45-55 interleukin 1 beta Rattus norvegicus 166-174 10406194-8 1999 FK506 markedly inhibited the nitric oxide formation, inducible nitric oxide synthase protein synthesis and inducible nitric oxide synthase mRNA expression induced by interleukin 1beta, but cyclosporin A had no effects. Tacrolimus 0-5 interleukin 1 beta Rattus norvegicus 166-183 12839866-20 2003 FK506 reduced IL-1beta and COX-2 mRNA expression and PGE(2) level in arthritic paws. Tacrolimus 0-5 interleukin 1 beta Rattus norvegicus 14-22 11045663-9 2000 The optimal doses of CsA and tacrolimus had similar inhibitory effects on Th1 type cytokine IL-2 and interferon [INF]-gamma), inflammatory cytokine (IL-1beta and tumor necrosis factor [TNF]-alpha), and cytotoxic factor (granzyme B and perforin) mRNA expression. Tacrolimus 29-39 interleukin 1 beta Rattus norvegicus 149-157 10510443-3 1999 Cyclosporin A and FK506 (at 1 microM) also significantly inhibited nitrite production induced by recombinant murine interferon-gamma (rIFNgamma) and recombinant murine interleukin-1beta (rIL-1beta) in J774 and VSMC, respectively. Tacrolimus 18-23 interleukin 1 beta Rattus norvegicus 187-196 10406194-3 1999 Studies were performed to determine whether the immunosuppressants FK506 and cyclosporin A directly influence gene expression of inducible nitric oxide synthase by interleukin 1beta in hepatocytes. Tacrolimus 67-72 interleukin 1 beta Rattus norvegicus 164-181 14528517-8 2003 FK506 caused a marked reduction of TNF-a and IL-1beta levels in paw tissue even in short-term (3-day) therapeutic treatment. Tacrolimus 0-5 interleukin 1 beta Rattus norvegicus 45-53 14528517-12 2003 CONCLUSION: FK506 is more effective than MTX in reducing elevated levels of inflammatory cytokines TNF-a, IL-1beta, and IL-6 in established stages of AIA. Tacrolimus 12-17 interleukin 1 beta Rattus norvegicus 106-114 7521274-5 1994 Both CsA and FK506 (at 1 mumol/L) significantly inhibited nitrite production induced by recombinant murine interleukin-1 beta (rIL-1 beta). Tacrolimus 13-18 interleukin 1 beta Rattus norvegicus 127-137 8971291-12 1996 Water immersion stress increased gastric mucosal IL-1 beta and IL-2 contents 6 h after stress treatment, and these increases were prevented by FK506. Tacrolimus 143-148 interleukin 1 beta Rattus norvegicus 49-58