Component
LipoCol Forte red yeast rice preparation studied in 2012
Context-specific entity; species, compartment and exposure are stated on each claim.
4 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.
Other things that act on it
Enzymes, hormones, genes, and other components with a recorded effect. These are not nutrients, so they do not count toward the arrows above. Each finding names the chapter that recorded it.
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.
What it acts on
In 14 volunteers, single doses of one, two or four LipoCol Forte capsules produced dose-related lovastatin and lovastatin-acid exposure; one capsule twice daily for five days produced no significant accumulation.
Experimental context and source evidence
- availability_state
- biomarker_context Imported condition classification; unverified.
- evidence_access
- Primary full text PMC3513969
- experimental_model
- Human fed-state dose and repeat-dose study; 600 mg per capsule.
- limitations
- Does not establish identical kinetics for other formulations, chronic use or interacting-drug conditions.
- nutrient_topic
- Red yeast rice collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · Red yeast rice
- plain_language
- The measured product had a defined short-term exposure profile.
- primary_references
- [23227093] Interaction between Red Yeast Rice and CYP450 Enzymes/P-Glycoprotein and Its Implication for the Clinical Pharmacokinetics of Lovastatin. · 2012 · https://pubmed.ncbi.nlm.nih.gov/23227093/ · DOI 10.1155/2012/127043
- trigger_kind
- biomarker_context Imported condition classification; unverified.
Red yeast rice: constituents, mevalonate, CoQ and product-specific interactions (2026-09-20) · lines 148–154
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Human fed-state dose and repeat-dose study; 600 mg per capsule. · source_derived_draft · unverified_draft
## red-yeast-rice-lipocol-dose-response The measured product had a defined short-term exposure profile. In 14 volunteers, single doses of one, two or four LipoCol Forte capsules produced dose-related lovastatin and lovastatin-acid exposure; one capsule twice daily for five days produced no significant accumulation. Model: Human fed-state dose and repeat-dose study; 600 mg per capsule. Limitations: Does not establish identical kinetics for other formulations, chronic use or interacting-drug conditions. Evidence access: Primary full text PMC3513969 [23227093] Interaction between Red Yeast Rice and CYP450 Enzymes/P-Glycoprotein and Its Implication for the Clinical Pharmacokinetics of Lovastatin. · 2012 · https://pubmed.ncbi.nlm.nih.gov/23227093/ · DOI 10.1155/2012/127043
Complete structured claim and evidenceOne 600 mg LipoCol Forte capsule did not significantly change the measured pharmacokinetics of 5 mg nifedipine in 14 volunteers.
Experimental context and source evidence
- evidence_access
- Primary full text PMC3513969
- experimental_model
- Human fasted-state single-dose pharmacokinetic comparison.
- limitations
- A null result for this dose does not exclude other drugs, preparations or exposures.
- nutrient_topic
- Red yeast rice collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · Red yeast rice
- plain_language
- The predicted enzyme interaction was not demonstrated in this tested regimen.
- primary_references
- [23227093] Interaction between Red Yeast Rice and CYP450 Enzymes/P-Glycoprotein and Its Implication for the Clinical Pharmacokinetics of Lovastatin. · 2012 · https://pubmed.ncbi.nlm.nih.gov/23227093/ · DOI 10.1155/2012/127043
Red yeast rice: constituents, mevalonate, CoQ and product-specific interactions (2026-09-20) · lines 156–162
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Human fasted-state single-dose pharmacokinetic comparison. · source_derived_draft · unverified_draft
## red-yeast-rice-nifedipine-null The predicted enzyme interaction was not demonstrated in this tested regimen. One 600 mg LipoCol Forte capsule did not significantly change the measured pharmacokinetics of 5 mg nifedipine in 14 volunteers. Model: Human fasted-state single-dose pharmacokinetic comparison. Limitations: A null result for this dose does not exclude other drugs, preparations or exposures. Evidence access: Primary full text PMC3513969 [23227093] Interaction between Red Yeast Rice and CYP450 Enzymes/P-Glycoprotein and Its Implication for the Clinical Pharmacokinetics of Lovastatin. · 2012 · https://pubmed.ncbi.nlm.nih.gov/23227093/ · DOI 10.1155/2012/127043
Complete structured claim and evidence
Where it participates (unsigned role)
Gemfibrozil 600 mg twice daily increased lovastatin-acid peak concentration and exposure area after LipoCol Forte in 13 volunteers.
Experimental context and source evidence
- availability_state
- biomarker_context Imported condition classification; unverified.
- evidence_access
- Primary full text PMC3513969
- experimental_model
- Human short-course gemfibrozil followed by one LipoCol Forte capsule.
- limitations
- The trial did not establish a unique responsible transporter or enzyme, nor measure a muscle-injury incidence.
- nutrient_topic
- Red yeast rice collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · Red yeast rice
- plain_language
- A coadministered drug increased exposure to the active acid.
- primary_references
- [23227093] Interaction between Red Yeast Rice and CYP450 Enzymes/P-Glycoprotein and Its Implication for the Clinical Pharmacokinetics of Lovastatin. · 2012 · https://pubmed.ncbi.nlm.nih.gov/23227093/ · DOI 10.1155/2012/127043
- trigger_kind
- biomarker_context Imported condition classification; unverified.
Red yeast rice: constituents, mevalonate, CoQ and product-specific interactions (2026-09-20) · lines 164–170
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Human short-course gemfibrozil followed by one LipoCol Forte capsule. · source_derived_draft · unverified_draft
## red-yeast-rice-gemfibrozil-acid A coadministered drug increased exposure to the active acid. Gemfibrozil 600 mg twice daily increased lovastatin-acid peak concentration and exposure area after LipoCol Forte in 13 volunteers. Model: Human short-course gemfibrozil followed by one LipoCol Forte capsule. Limitations: The trial did not establish a unique responsible transporter or enzyme, nor measure a muscle-injury incidence. Evidence access: Primary full text PMC3513969 [23227093] Interaction between Red Yeast Rice and CYP450 Enzymes/P-Glycoprotein and Its Implication for the Clinical Pharmacokinetics of Lovastatin. · 2012 · https://pubmed.ncbi.nlm.nih.gov/23227093/ · DOI 10.1155/2012/127043
Complete structured claim and evidenceGemfibrozil did not significantly change parent lovastatin pharmacokinetic parameters in that LipoCol Forte experiment.
Experimental context and source evidence
- evidence_access
- Primary full text PMC3513969
- experimental_model
- Same 13 volunteers and dosing protocol.
- limitations
- The positive acid result must not be generalized to every measured chemical form.
- nutrient_topic
- Red yeast rice collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · Red yeast rice
- plain_language
- The lactone and acid did not show the same interaction result.
- primary_references
- [23227093] Interaction between Red Yeast Rice and CYP450 Enzymes/P-Glycoprotein and Its Implication for the Clinical Pharmacokinetics of Lovastatin. · 2012 · https://pubmed.ncbi.nlm.nih.gov/23227093/ · DOI 10.1155/2012/127043
Red yeast rice: constituents, mevalonate, CoQ and product-specific interactions (2026-09-20) · lines 172–178
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Same 13 volunteers and dosing protocol. · source_derived_draft · unverified_draft
## red-yeast-rice-gemfibrozil-lactone-null The lactone and acid did not show the same interaction result. Gemfibrozil did not significantly change parent lovastatin pharmacokinetic parameters in that LipoCol Forte experiment. Model: Same 13 volunteers and dosing protocol. Limitations: The positive acid result must not be generalized to every measured chemical form. Evidence access: Primary full text PMC3513969 [23227093] Interaction between Red Yeast Rice and CYP450 Enzymes/P-Glycoprotein and Its Implication for the Clinical Pharmacokinetics of Lovastatin. · 2012 · https://pubmed.ncbi.nlm.nih.gov/23227093/ · DOI 10.1155/2012/127043
Complete structured claim and evidence
The events it takes part in
A mechanism often involves more than two components. These are the full events, with every participant and its role.
Situations it appears in
Low-supply and faulty-machinery situations recorded in the chapters where this component plays a part.
In the sources
Preserved passages that mention this component, quoted exactly. Open one to read it in context.
Open hypotheses
Proposed ideas that involve this component. They are labeled as hypotheses and do not change any recorded statement.
This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.