Effect of quercetin on the pharmacokinetics of rosiglitazone, a CYP2C8 substrate, in healthy subjects
Placebo-controlled crossover drug-interaction study. Rosiglitazone exposure and its metabolic ratio were similar with quercetin and placebo.
Records 261–290 of 290. Open a study to inspect the full evidence record. Source links lead directly to the publication. Updated 19 October 2026.
Safety, interactions and special populations (4) · Kidney and cancer research (2) · Forms, absorption and food sources (14) · Prostate and urinary health (2) · Evidence reviews and human mechanisms (2) · Cardiovascular and metabolic health (3) · Skin and topical formulations (2) · Gut and intestinal health (1)
Placebo-controlled crossover drug-interaction study. Rosiglitazone exposure and its metabolic ratio were similar with quercetin and placebo.
Pilot human supplementation study with ex vivo platelet assays. Platelet aggregation and selected collagen-signaling responses were reduced after ingestion.
Randomized dietary crossover study with supporting platelet experiments. Neither food intervention changed measured hemostatic outcomes, although high concentrations inhibited platelets in vitro.
Random-order human pharmacokinetic comparison. Grapefruit juice increased nifedipine exposure; quercetin did not, although absorption timing was delayed.
Randomized placebo-controlled renal-transplant trial. Early graft-function measures favored the combination, with lower creatinine in the higher-dose group.
Phase 1 intravenous oncology dose-escalation study. Tyrosine-phosphorylation inhibition was observed, and renal toxicity became dose limiting at high intravenous exposure.
Original sources: PubMed
Randomized parallel dietary intervention. Berry intake increased serum quercetin concentrations.
Controlled crossover dietary biomarker study. Plasma quercetin did not change significantly between these dietary conditions, while citrus flavanone concentrations did.
Early clinical pharmacokinetic study with supporting preclinical work. The oral prodrug produced no detectable plasma exposure; intravenous administration released measurable quercetin.
Four-way crossover human absorption study. Glucoside-containing treatments produced earlier, higher plasma conjugate concentrations than rutin-containing treatments; free quercetin was not detected.
Human radiolabeled disposition and mass-balance study. A substantial fraction of radiolabel appeared as exhaled carbon dioxide, showing extensive metabolism beyond urinary quercetin conjugates.
Human crossover glucoside absorption comparison. The two glucosides had similar bioavailability and rapid peak concentrations.
Human ileostomy absorption and hydrolysis experiment. Intact glucosides were not detected in effluent; recovered aglycone supported extensive intestinal hydrolysis before absorption.
Double-blind diet-controlled crossover pharmacokinetic study. Aglycone was absorbed earlier; rutin had more variable absorption. Overall exposure was similar in this experiment, and metabolites predominated.
Acute dietary absorption and antioxidant pilot. Plasma quercetin and one antioxidant-capacity measure increased, but LDL oxidation susceptibility did not improve.
Crossover juice dose-response study. Urinary quercetin increased, while oxidative-stress measures showed mixed directions, including increased protein oxidation.
Random-order crossover dietary biomarker study. Plasma and urinary flavonols reflected short-term intake; recovery differed between tea and onions.
Human bioavailability synthesis describing dietary absorption experiments. Absorption and timing differed across glycosides and foods; onion-derived glucosides were absorbed more readily than rutin in the reported experiments.
Random-order crossover absorption study in ileostomy volunteers. Estimated intestinal absorption was higher from onion glucosides than rutin or aglycone under this method.
Early human oral and intravenous disposition study. The older assay detected rapid intravenous disposition but no measurable oral plasma quercetin; fecal recovery suggested extensive gut metabolism.
Open-label uncontrolled interstitial-cystitis pilot. Symptoms, problem scores, and global pain ratings improved from baseline.
Original sources: PubMed
Clinical narrative review of chronic prostatitis/chronic pelvic pain syndrome. The review discusses quercetin as one possible component of multimodal chronic pelvic pain care.
Placebo-controlled short-term human biomarker study. TIMP-1 expression and concentration decreased; MMP-2 and TIMP-2 did not change.
Randomized crossover dietary intervention. Plasma quercetin increased on the high-flavonol diet, but oxidative DNA damage in leukocytes did not decrease.
Original sources: PubMed
Prospective observational dietary cohort. Quercetin intake was not associated with cerebrovascular disease incidence; an apple association was not explained by quercetin.
Randomized parallel supplementation comparison after a placebo run-in. Ex vivo LDL resistance to copper-induced oxidation increased; plasma lipid levels did not change.
Original sources: PubMed
Double-blind placebo-controlled supplementation study. Plasma quercetin rose markedly, but lipids, blood pressure, platelet measures, and other selected cardiovascular-risk markers did not improve.
Mouse topical intervention with single-cell and mechanistic analyses. Topical quercetin promoted hair-follicle regeneration in mice and altered follicular and vascular signatures.
Published correction linked to the mouse hair-regeneration paper. The publication corrects the earlier hair-regeneration report and must be read alongside it.
Dietary intervention and intestinal mechanism study in mice. Quercetin improved selected intestinal-barrier, inflammatory and signalling measures in high-fat-fed mice.
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