Component

Rat interleukin-10 expression

Rat interleukin-10 expression. Species, exposure and limitations are retained in each linked claim.

1 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

Tracing routes…

What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What acts on it

  1. Theanine increased the anti-inflammatory IL-10 response in the tested normal/stressed rat pathways.

    L-Theanine → Rat interleukin-10 expression source_derived_draftungraded
    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/theanine-research/34037653.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "c792377afacbf5a17e93e4675a4a28ee6849d0288bfc09ad53a2377a0bb982b1", "start_char": 0, "end_char": 1786, "text_sha256": "c792377afacbf5a17e93e4675a4a28ee6849d0288bfc09ad53a2377a0bb982b1"}
    experimental_model
    Receptor interaction and pathway assays
    exposure
    Theanine; normal versus experimental stress conditions
    limitations
    Preclinical CB1-binding claim requires independent confirmation at human exposures; signaling direction differed between normal and stressed rats. No equivalence to cannabinoid drugs inferred.
    nutrient_topic
    L-Theanine research collection; topical membership is not evidence of a direct dietary effect. · L-Theanine
    organism
    Normal and E44813-stressed rats
    plain_language
    A specific cytokine endpoint changed in the experiment; broad human immune benefit is not established.
    primary_references
    [theanine-p34037653] L-Theanine regulates glutamine metabolism and immune function by binding to cannabinoid receptor 1. (2021). https://pubmed.ncbi.nlm.nih.gov/34037653/ DOI: 10.1039/d1fo00505g
    tissue_or_cell_type
    CB1-associated immune and glutamine regulation

    L-Theanine: metabolism, neural signaling, nutrient connections and human outcomes (2026-09-17) · lines 497–508

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Receptor interaction and pathway assays · source_derived_draft · unverified_draft

    ### theanine-rat-il10 Theanine increased the anti-inflammatory IL-10 response in the tested normal/stressed rat pathways. Condition category: normal nutrient_topic: L-Theanine research collection; topical membership is not evidence of a direct dietary effect. plain_language: A specific cytokine endpoint changed in the experiment; broad human immune benefit is not established. organism: Normal and E44813-stressed rats tissue_or_cell_type: CB1-associated immune and glutamine regulation experimental_model: Receptor interaction and pathway assays limitations: Preclinical CB1-binding claim requires independent confirmation at human exposures; signaling direction differed between normal and stressed rats. No equivalence to cannabinoid drugs inferred. exposure: Theanine; normal versus experimental stress conditions evidence_span: {"source_cache": "artifacts/theanine-research/34037653.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "c792377afacbf5a17e93e4675a4a28ee6849d0288bfc09ad53a2377a0bb982b1", "start_char": 0, "end_char": 1786, "text_sha256": "c792377afacbf5a17e93e4675a4a28ee6849d0288bfc09ad53a2377a0bb982b1"} [theanine-p34037653] L-Theanine regulates glutamine metabolism and immune function by binding to cannabinoid receptor 1. (2021). https://pubmed.ncbi.nlm.nih.gov/34037653/ DOI: 10.1039/d1fo00505g
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.

    Evidence, AI assistance and curation standards