Ovine Liver Extract
Ovine liver extract is a preparation derived from sheep liver containing folates, heat-stable proteins, and iron-binding compounds isolated through biochemical fractionation techniques. Its bioactive constituents include ion-exchange-separated folate forms and ammonium sulfate-fractionated proteins, though no controlled clinical trials have established human health benefits.

Origin & History
Ovine liver extract is derived from sheep (Ovis aries) liver through processes including homogenization, enzymatic hydrolysis, or heat treatment followed by filtration and concentration. Production involves mincing frozen sheep liver, homogenizing in lysis buffer, centrifuging, optional boiling at 95°C for 7-10 minutes, and concentrating filtrates to >70% total solids, meeting Chinese national drug standard WS-10001-(HD-0812)-2002.
Historical & Cultural Context
No historical or traditional medicinal uses of ovine liver extract are documented in the available sources. All references are limited to modern extraction and preparation methods without traditional context.
Health Benefits
• No clinical health benefits documented - available research focuses solely on extraction methods and biochemical analysis • Contains folates (separated by ion-exchange chromatography) - evidence quality: biochemical analysis only • Source of heat-stable proteins (isolated via ammonium sulfate fractionation) - evidence quality: laboratory characterization only • Contains enzymes including 6-phosphogluconate dehydrogenase and β-galactosidase - evidence quality: purification studies only • Meets Chinese drug quality standards WS-10001-(HD-0812)-2002 - evidence quality: regulatory compliance only
How It Works
The folate compounds isolated from ovine liver extract via ion-exchange chromatography are structurally capable of serving as one-carbon donors in methylation reactions, supporting methionine synthesis from homocysteine via methionine synthase. Heat-stable proteins recovered through ammonium sulfate fractionation may include heme-binding and iron-transport proteins such as ferritin precursors, potentially facilitating intracellular iron storage via ferroportin-mediated pathways. These mechanisms are inferred from biochemical characterization studies rather than demonstrated pharmacokinetic or receptor-binding data in humans.
Scientific Research
No human clinical trials, randomized controlled trials, or meta-analyses on ovine liver extract were identified in the research. Available studies focus exclusively on extraction methodology and enzyme purification, such as 6-phosphogluconate dehydrogenase isolation (PMID: 1821813), without any clinical outcome data.
Clinical Summary
No randomized controlled trials, observational cohort studies, or human pharmacokinetic studies have been conducted using ovine liver extract as a standardized supplement. Available research is limited entirely to in vitro biochemical analyses examining extraction methodology, including ion-exchange chromatography for folate isolation and ammonium sulfate fractionation for protein recovery. Evidence quality is classified as biochemical analysis only, placing it at the lowest tier of clinical evidence hierarchy. Any attributed health benefits are extrapolated from the known functions of isolated constituents rather than direct supplementation outcomes.
Nutritional Profile
Ovine (sheep) liver extract is a concentrated protein-rich fraction derived from sheep liver tissue. Macronutrients: High protein content (estimated 60–80% dry weight after extraction), predominantly heat-stable proteins isolated via ammonium sulfate fractionation; lipid content variable but generally low post-extraction (<5% dry weight); carbohydrate content minimal (<2% dry weight). Micronutrients: Folates present at biologically relevant concentrations (separated and confirmed via ion-exchange chromatography); vitamin B12 (cobalamin) expected given hepatic origin, typical of ruminant liver extracts (~50–100 µg/100g raw liver equivalent, though concentration varies by extraction method); iron (heme-bound, high bioavailability ~15–35% absorption vs. non-heme ~5–12%); zinc (~4–6 mg/100g raw equivalent, good bioavailability from animal sources); copper (~10–15 mg/100g raw equivalent, notably high in ruminant liver); riboflavin (B2) (~3–4 mg/100g raw equivalent); retinol (preformed vitamin A, potentially very high in concentrated extracts, >10,000 IU/100g equivalent — toxicity risk at high doses). Bioactive compounds: Enzymes including 6-phosphogluconate dehydrogenase and other hepatic enzymes (activity dependent on extraction temperature and pH); coenzyme Q10 trace amounts; glutathione and related thiol compounds. Bioavailability notes: Heme iron and zinc from ovine liver demonstrate superior bioavailability compared to plant sources; folate bioavailability from animal tissue is generally high (~80–90%); enzyme activity in extracts is highly dependent on processing conditions — heat-stable fractions retain functional activity post-fractionation, while labile enzymes may be denatured; retinol concentration warrants caution in concentrated extracts due to potential hypervitaminosis A risk. Overall nutritional characterization is based on biochemical analysis and extrapolation from raw ovine liver composition, as clinical bioavailability data specific to ovine liver extract preparations is not documented.
Preparation & Dosage
No clinically studied dosage ranges for ovine liver extract have been established in human trials. Manufacturing yields of 1.1-1.36 kg paste from unspecified starting liver amounts are described, but therapeutic dosing guidelines are absent. Consult a healthcare provider before starting any new supplement.
Synergy & Pairings
Insufficient evidence for synergistic combinations
Safety & Interactions
No formal safety profile, toxicology studies, or adverse event reporting exists specifically for ovine liver extract supplements in humans. As a liver-derived animal product, it carries theoretical risk of excess preformed vitamin A (retinol) accumulation, which is teratogenic at high doses and contraindicated during pregnancy. Individuals on methotrexate or other antifolate medications should exercise caution given the folate content, as supplemental folates can antagonize these drugs' mechanisms. People with hemochromatosis or iron overload disorders should avoid liver-derived extracts due to potential iron loading from hepatic iron-binding proteins.