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Relationship: 2353
Title
Bradykinin, activated leads to Increased proinflammatory mediators
Upstream event
Downstream event
AOPs Referencing Relationship
| AOP Name | Adjacency | Weight of Evidence | Quantitative Understanding | Point of Contact | Author Status | OECD Status |
|---|---|---|---|---|---|---|
| Decreased fibrinolysis and activated bradykinin system leading to hyperinflammation | adjacent | Cataia Ives (send email) | Under development: Not open for comment. Do not cite | Under Development |
Taxonomic Applicability
| Term | Scientific Term | Evidence | Link |
|---|---|---|---|
| human | Homo sapiens | High | NCBI |
Sex Applicability
Life Stage Applicability
Bradykinin (BK) plays an important role in the kinin-kallikrein system (KKS) as a regulator of blood pressure and can induce vasodilation, increase blood flow, as well as hypotension. BK is also an important part of the inflammatory process after injury, induces pain stimulation, and increases vascular permeability (Maas, 10.1007/s12016-016-8540-0).
The bradykinin system gets activated through various methods, including nanoparticles and SARS-COV-2 via the contact activation system (Maas, 10.1007/s12016-016-8540-0, Ekdahl doi: 10.1080/14686996.2019.1625721). Activation of the bradykinin system leads to increase of proinflammatory mediators due to increased production of proinflammatory mediator bradykinin(https://doi.org/10.1161/01.CIR.95.5.1115) as well as upregulating bradykinin receptor 1 (BDKRB1) and 2(BDKRB2), leading to induction of proinflammatory mediators such as IL-2, IL-6 and IL-8 (https://doi.org/10.1165/rcmb.2002-0040OC) and the activation of the NFKb pathway leading to production of proinflammatory mediators TNF and IL1(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC507648/).
| ID | Experimental Design | Species | Upstream Observation | Downstream Observation | Citation (first author, year) | Notes |
|---|
| Title | First Author | Biological Plausibility |
Dose Concordance |
Temporal Concordance |
Incidence Concordance |
|---|