Evidence-based·Last reviewed May 31, 2026·How we grade evidence

Ornithine alpha-ketoglutarate

Amino-acidSalt

A salt of 2 ornithine molecules with 1 α-ketoglutarate, originally developed as a clinical-nutrition compound for hospitalized catabolic patients (burns, trauma, sepsis, elderly malnutrition). Provides building blocks for arginine, glutamine, proline, and polyamines that drive wound healing and protein anabolism. Strongest evidence is from burn-unit RCTs (De Bandt 1998, Coudray-Lucas 2000) showing faster wound closure and improved nitrogen balance. Consumer 'sports performance' claims rest on mechanism, not direct outcomes.

Quick decision guide

May help most

Hospitalized patients with severe burns or trauma (under clinical supervision); elderly patients with malnutrition or pressure ulcers. Not a typical consumer supplement.

Common dosing range

Clinical: 10–30 g/day enteral. Consumer (off-label): 2–5 g/day pre-workout for purported anabolic effect (low-quality evidence).

When to expect effects

Weeks for wound-healing effects in clinical settings; rapid (hours) for amino-acid availability.

Watch out for

Primarily a clinical-nutrition compound. GI upset (cramping, diarrhea) common above 10 g/day. Avoid in renal or hepatic impairment without clinical supervision.

Evidence snapshot

Severe burn — wound healing and nitrogen balanceModerate
Elderly malnutrition / pressure ulcersModerate
Trauma / post-surgical catabolismEmerging
Athletic performance / muscle gainLow
Hepatic encephalopathyLow

What is it

Ornithine alpha-ketoglutarate (OKG, ornithine oxoglutarate) is a salt formed from two molecules of the non-proteinogenic amino acid L-ornithine and one molecule of alpha-ketoglutarate (a Krebs-cycle intermediate). After ingestion it dissociates into its component parts, which feed converging biochemical pathways: ornithine enters the urea cycle and can be converted to glutamate, polyamines, proline, and arginine, while alpha-ketoglutarate serves as a substrate for the tricarboxylic acid cycle, amino acid transamination, and collagen-related prolyl hydroxylase reactions. Together, these substrates are thought to support anti-catabolic, anabolic, and ammonia-buffering effects, the rationale for OKG's historical use in clinical nutrition for burn injury, surgical recovery, and undernourished elderly patients.

Is it worth it for you?

Use this as a quick fit check, not a diagnosis.

Worth considering if

You're hospitalized with severe burns and your medical team is using clinical-nutrition protocols — OKG has direct RCT support
You're an elderly malnourished patient or recovering from major surgery, under clinical supervision
Your clinician has recommended OKG for pressure ulcer healing or muscle catabolism prevention

Probably skip if

You're a healthy adult looking for a workout pre-supplement — better evidence exists for creatine, caffeine, and beta-alanine
You expect 'natural HGH release' from OKG — early small studies were not replicated reliably
You have kidney or liver disease — ornithine and α-ketoglutarate both load the urea cycle and need clinical oversight
You're hoping it will reverse age-related sarcopenia by itself — protein adequacy and resistance training matter much more

Evidence at a glance

Severe burn injury — wound healing & nitrogen balance

Good Evidence
Effect
Wound healing time 60 vs 90 days (Coudray-Lucas); improved nitrogen balance and reduced muscle catabolism markers
Best fit
Hospitalized severe burn patients receiving enteral nutrition
Time
Weeks (significant wound-healing differences emerge by 3–4 weeks)

Elderly malnutrition / pressure ulcer healing

Good Evidence
Effect
Significantly accelerated pressure ulcer surface area reduction in elderly at 10 g/day for 6 weeks
Best fit
Elderly hospitalized or institutionalized patients with malnutrition, pressure ulcers, or post-acute recovery
Time
4–6 weeks

Hepatic encephalopathy / ammonia metabolism

Limited Evidence
Effect
Reduces blood ammonia mechanistically (closely related to LOLA, which has HE trial data)
Best fit
None established for OKG specifically in HE (LOLA is the studied form)
Time
Not established for OKG in HE

Athletic performance / muscle gain

Mixed Evidence
Effect
No reliable improvement in performance or lean mass in well-controlled trials in healthy adults
Best fit
None established for healthy athletes
Time
Not established

Evidence for 4 uses

AI-assisted evidence assessment — talk to your doctor before relying on any single supplement.

Severe burn injury — wound healing & nitrogen balance

Disease adjunct
Good Evidence

OKG has direct RCT evidence in burn-unit settings. De Bandt 1998 in 54 patients with 2050% total burn surface area showed OKG (1030 g/day enteral) improved nitrogen balance and reduced 3-methylhistidine and hydroxyproline urinary elimination (markers of protein catabolism). Bolus administration significantly accelerated wound healing (last graft at day 23.7 vs 39.9 in controls). Coudray-Lucas 2000 reported wound healing time of 60 ± 7 days with OKG vs 90 ± 12 days with isonitrogenous control. Mechanism: ornithine is a direct precursor of arginine, proline, and polyamines (all required for collagen deposition and cell proliferation); α-ketoglutarate is a glutamine precursor and nitrogen scavenger.

Effect size
Wound healing time 60 vs 90 days (Coudray-Lucas); improved nitrogen balance and reduced muscle catabolism markers
Time to effect
Weeks (significant wound-healing differences emerge by 3–4 weeks)
Best fit
Hospitalized severe burn patients receiving enteral nutrition
Less likely
Outpatient or minor burns — clinical-nutrition formulations not indicated

Bottom line: Direct RCT evidence in hospital burn units. Not a consumer indication — used under clinical supervision.

Elderly malnutrition / pressure ulcer healing

Disease adjunct
Good Evidence

The Meaume 2009 RCT (n=200) in elderly patients with heel pressure ulcers compared OKG 10 g/day for 6 weeks against placebo, and reported significantly faster wound surface area reduction with good tolerability. Earlier Brocker 1994 work in 194 convalescent elderly showed OKG-supplemented patients had improved functional status and appetite vs controls. Ornithine precursor of arginine and proline is biologically logical for collagen-dependent wound healing.

Effect size
Significantly accelerated pressure ulcer surface area reduction in elderly at 10 g/day for 6 weeks
Time to effect
4–6 weeks
Best fit
Elderly hospitalized or institutionalized patients with malnutrition, pressure ulcers, or post-acute recovery
Less likely
Healthy older adults — protein-adequate diet matters more

Bottom line: Reasonable adjunct in clinical-nutrition protocols for malnourished or wound-healing elderly patients.

Hepatic encephalopathy / ammonia metabolism

Mechanism only
Limited Evidence

L-ornithine L-aspartate (LOLA, a different ornithine salt) has clinical use in hepatic encephalopathy, lowering ammonia via stimulation of urea-cycle enzymes and glutamine synthesis. OKG shares some mechanism but is not the form used in hepatic encephalopathy trials. Mechanism is plausible; direct OKG outcome evidence in HE is limited.

Effect size
Reduces blood ammonia mechanistically (closely related to LOLA, which has HE trial data)
Time to effect
Not established for OKG in HE
Best fit
None established for OKG specifically in HE (LOLA is the studied form)
Less likely
Patients with hepatic encephalopathy — use evidence-based therapies (lactulose, rifaximin, LOLA in some settings)

Bottom line: Related compound (LOLA) is studied in HE; OKG itself isn't the standard. Use evidence-based therapy.

Athletic performance / muscle gain

Mechanism only
Mixed Evidence

Marketed for sports performance based on the theory that OKG enhances growth-hormone release and anabolism. Early small studies suggested OKG might raise insulin and growth hormone, but larger and better-controlled trials in healthy athletes have not consistently shown improvements in strength, lean mass, or power output beyond what creatine, protein adequacy, and resistance training already deliver. Mechanism-based, not outcome-validated, for performance use.

Effect size
No reliable improvement in performance or lean mass in well-controlled trials in healthy adults
Time to effect
Not established
Best fit
None established for healthy athletes
Less likely
Healthy adults — creatine and adequate protein dominate the evidence base

Bottom line: Mostly mechanism-only marketing. Healthy adults should prioritize creatine and protein adequacy first.

How to take it

1. Typical dose
• Clinical (burn / catabolic): 10–30 g/day enteral, under supervision • Elderly malnutrition / pressure ulcers: 10 g/day for 6 weeks (Meaume protocol) • Consumer (off-label, weak evidence): 2–5 g pre-workout • Always with food to reduce GI upset
2. Higher studied dose
Up to 30 g/day in burn-unit RCTs. Doses above 10 g/day commonly cause GI upset (cramping, nausea, diarrhea) in non-hospital settings — split into 2–3 daily doses.
3. Timing
With meals to improve tolerance. Pre-workout dosing (consumer use) has no real outcome support.
4. With food
With food.
5. Split dosing
Split 2–3×/day if using >5 g/day. Burn-unit protocols often divide into multiple enteral feeds.
6. How long to try
Burn / pressure ulcer trials ran 4–6 weeks. Chronic outpatient use beyond 6 weeks is not well studied.

What to track

Wound surface area / healing progress (clinical setting)
GI tolerance — cramping, diarrhea at higher doses
Nitrogen balance markers in clinical-nutrition workup
Renal function if on long-term high-dose (urea cycle load)

Bottom line: Use under clinical supervision for the supported indications (burns, malnutrition, pressure ulcers). Not a high-value consumer supplement.

4 commercial forms

Compare the main delivery options and what they’re best suited for.

Ornithine alpha-ketoglutarate (OKG)

Clinical compound

Salt of 2 ornithine molecules with 1 α-ketoglutarate. The form used in burn-unit RCTs (De Bandt, Coudray-Lucas) and elderly malnutrition trials (Meaume). Available as Cetornan in some clinical-nutrition markets.

Standard clinical-nutrition compound; orally bioavailable as separate amino acids after absorption.

L-ornithine HCl

Plain ornithine

Just the ornithine portion. Marketed for 'GH release' and sleep aid. Less direct clinical evidence than OKG; modest effect on plasma ornithine and arginine.

Well-absorbed; doesn't provide the α-KG nitrogen-scavenging effect.

L-ornithine L-aspartate (LOLA)

Used in liver disease

Different ornithine salt with α-amino acid aspartate instead of α-KG. Has clinical use for hepatic encephalopathy under medical care. Different mechanism focus than OKG.

Available as prescription in some countries; oral/IV.

Alpha-ketoglutaric acid (AKG)

Just α-KG

Just the α-ketoglutarate side. Used for purported longevity/aging research (e.g., calcium-AKG products). Different from OKG.

Calcium salt commonly used; rapid absorption.

Safety

Know the common side effects, key cautions, and who should avoid it.

Common side effects

nauseaabdominal crampingdiarrhea (dose-dependent)mild stomach upset

Serious risks

Who should avoid it

Pregnancy & breastfeeding

OKG safety in pregnancy is not established. As a clinical-nutrition compound it would only be used in pregnancy under specialist supervision (e.g., a severely burned pregnant patient in ICU). Routine consumer use in pregnancy is not appropriate.

Bottom line: Primarily a clinical-nutrition compound. GI side effects are dose-dependent. Renal or hepatic impairment requires clinical oversight.

Interactions

renal-cleared medicationsMinor

OKG metabolism loads the urea cycle and may affect renal handling of other compounds. No specific established drug interactions but caution in renal impairment.

lactulose / rifaximin (hepatic encephalopathy therapy)Minor

Both lower ammonia by different mechanisms. Use of OKG alongside without specialist guidance is not standard.

growth hormone or insulin therapyMinor

OKG marketed (off-label) for GH-promoting effect; theoretical additive effects if combined with prescribed GH or insulin. No reliable clinical interactions documented.

Food sources

Ornithine alpha-ketoglutarate

Amount
Pharmaceutical/supplement only
%DV

Choosing a product

What to look for on the label — and what to be skeptical of.

Look for

Clear ornithine and α-ketoglutarate content per serving (2 ornithine : 1 α-KG ratio)
Pharmaceutical-grade if used for clinical purposes (Cetornan was the French clinical-nutrition product)
Third-party tested (USP, NSF, ConsumerLab)
Powder or capsule form; powder allows clinical-grade dosing flexibility

Be skeptical of

'Natural HGH booster' — small early studies not consistently replicated in athletes
'Burns fat / builds muscle' — outcome evidence in healthy adults is weak
Marketing for 'anti-aging' or 'longevity' — not supported by current evidence
Mega-dose products (10+ g per scoop) marketed for daily use — GI tolerability concerns
Combination 'recovery' products that bundle OKG with many other compounds at sub-evidence-based individual doses

References by claim

Severe burn injury — wound healing & nitrogen balance

De Bandt et al., 1998J Nutr — Mode of enteral OKG administration in burn patients (1998) link

Coudray-Lucas et al., 2000Burns — OKG improves wound healing in severe burn patients (2000) link

Elderly malnutrition / pressure ulcer healing

Meaume et al., 2009J Nutr Health Aging — OKG in heel pressure ulcers in elderly (2009) link

Athletic performance / muscle gain

Cynober, 1991Nutrition — OKG in nutritional support review (1991) link

Other references

Wikidata: ornithine oxoglutarate (Q7103624)Wikidata link

PubChem CID 78866: Ornithine alpha-ketoglutaratePubChem link

NIH DSLD: Ornithine Alpha-KetoglutarateNIH Dietary Supplement Label Database link

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Evidence-based·Last reviewed May 31, 2026·Evidence current as of May 31, 2026·How we grade evidence

Disclaimer: These statements have not been evaluated by the FDA. This page is educational, not a substitute for personalized medical advice. Evidence grades are AI-assisted assessments — talk to your doctor before starting any new supplement, especially if you’re pregnant, breastfeeding, on medications, or managing a chronic condition.