Component

Rat liver microsomes

Rat liver microsomes. 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

Where it participates (unsigned role)

  1. After two weeks of dihydrocapsaicin at 10 mg/kg/day the area under the plasma concentration-time curve for efavirenz increased from 8821 to 22347 micrograms per millilitre per hour, time to maximum plasma concentration increased from 2.50 to 3.50 hours and elimination half-life from 3.13 to 3.51 hours, while plasma clearance fell from 6.71 to 2.65 litres per hour per kilogram, and dihydrocapsaicin significantly inhibited the metabolism of efavirenz in rat liver microsomes; the authors conclude the dose should be monitored in patients on efavirenz maintenance therapy.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/dihydrocapsaicin-research/41286578.abstract.txt", "locator": "Indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "9063b8f1265e2ca00078e7452f81fc480eea4995c88a595cfbd42d245e74f68e", "start_char": 0, "end_char": 1538, "text_sha256": "9063b8f1265e2ca00078e7452f81fc480eea4995c88a595cfbd42d245e74f68e"}
    experimental_model
    Twelve Sprague-Dawley rats pretreated for two weeks, with rat liver microsome experiments
    exposure
    Dihydrocapsaicin 10 mg/kg/day for two weeks before a single oral 56 mg/kg dose of efavirenz
    limitations
    A named drug interaction with both in vivo and in vitro arms. Twelve rats in two groups, and a rat liver microsome system rather than a human one.
    nutrient_topic
    Dihydrocapsaicin research collection; topical membership is not evidence of a direct clinical effect, and dihydrocapsaicin is recorded separately from capsaicin. · Dihydrocapsaicin
    organism
    Rat
    plain_language
    Two weeks of the compound left two and a half times as much of an HIV drug in the blood.
    primary_references
    [dhc-p41286578] Impact of Dihydrocapsaicin on the Metabolism of Efavirenz In Vitro and In Vivo. (2025). https://pubmed.ncbi.nlm.nih.gov/41286578/ DOI: 10.1002/prp2.70189
    tissue_or_cell_type
    Liver and plasma

    Dihydrocapsaicin: the second capsaicinoid, the hypothermia it is used to induce, what the gut and liver do to it, and what it does without TRPV1 (2026-09-21) · lines 595–606

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Twelve Sprague-Dawley rats pretreated for two weeks, with rat liver microsome experiments · source_derived_draft · unverified_draft

    ### dhc-efavirenz-interaction After two weeks of dihydrocapsaicin at 10 mg/kg/day the area under the plasma concentration-time curve for efavirenz increased from 8821 to 22347 micrograms per millilitre per hour, time to maximum plasma concentration increased from 2.50 to 3.50 hours and elimination half-life from 3.13 to 3.51 hours, while plasma clearance fell from 6.71 to 2.65 litres per hour per kilogram, and dihydrocapsaicin significantly inhibited the metabolism of efavirenz in rat liver microsomes; the authors conclude the dose should be monitored in patients on efavirenz maintenance therapy. Condition category: normal nutrient_topic: Dihydrocapsaicin research collection; topical membership is not evidence of a direct clinical effect, and dihydrocapsaicin is recorded separately from capsaicin. plain_language: Two weeks of the compound left two and a half times as much of an HIV drug in the blood. organism: Rat tissue_or_cell_type: Liver and plasma experimental_model: Twelve Sprague-Dawley rats pretreated for two weeks, with rat liver microsome experiments limitations: A named drug interaction with both in vivo and in vitro arms. Twelve rats in two groups, and a rat liver microsome system rather than a human one. exposure: Dihydrocapsaicin 10 mg/kg/day for two weeks before a single oral 56 mg/kg dose of efavirenz evidence_span: {"source_cache": "artifacts/dihydrocapsaicin-research/41286578.abstract.txt", "locator": "Indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "9063b8f1265e2ca00078e7452f81fc480eea4995c88a595cfbd42d245e74f68e", "start_char": 0, "end_char": 1538, "text_sha256": "9063b8f1265e2ca00078e7452f81fc480eea4995c88a595cfbd42d245e74f68e"} [dhc-p41286578] Impact of Dihydrocapsaicin on the Metabolism of Efavirenz In Vitro and In Vivo. (2025). https://pubmed.ncbi.nlm.nih.gov/41286578/ DOI: 10.1002/prp2.70189
    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