Apg8.0

Apigenin

Apigenin

A natural flavonoid from chamomile that promotes sleep and relaxation through GABA modulation.

sleepmentalsleepanxietyGABAchamomile
Last reviewed: January 1, 2025
8.0/10
37+ studies
Evidence
high
Safety
50mg before bed
Dose
1-4 weeks
Time to Effect
Apigenin extract capsules
Best Form

Apigenin is a flavonoid found in chamomile, parsley, and other plants. It binds to GABA receptors and has anxiolytic (anti-anxiety) and sleep-promoting effects. While direct human studies are limited, its mechanism is well-understood and it's a key reason chamomile has been used for sleep for centuries.

Mechanisms of Action

🧘
GABA-A Binding

Binds to GABA receptors for calming effects

🧬
CD38 Inhibition

May preserve NAD+ levels (longevity pathway)

πŸ”₯
Anti-Inflammatory

Reduces inflammatory markers

Recommended Dose

50mg before bed

25mg100mg

Optimal Timing

  • 30-60 minutes before bed

Can be taken without food

Best Form

Apigenin extract capsules

Alternatives: Chamomile extract (standardized), Chamomile tea (lower dose)

Pure apigenin provides consistent dosing. Chamomile extract should be standardized to apigenin content. Chamomile tea provides variable, lower doses (~3-10mg per cup).

Duration

Minimum: 1 weeks

Optimal: 4 weeks

Cycling: Not required

Note: Take before bed for sleep. Can be combined with other sleep supplements like magnesium and L-theanine.

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😌
Relaxation

Calm, relaxed feeling without heavy sedation

30-60 minutes
70% of users notice thispositive
😴
Easier Sleep Onset

Helps transition to sleep more easily

30-60 minutes
65% of users notice thispositive
πŸ”
Subtle Effects

Effects are gentle; not a strong sedative

N/A
85% of users notice thisneutral
High SafetyMax safe dose: Up to 100mg commonly used; higher doses less studied
🟑
Pregnant/nursing

Chamomile tea is common during pregnancy; concentrated supplements less studied

πŸ”΄
Ragweed allergy

May cross-react; avoid or use caution

Who Should NOT Take This

  • Allergy to chamomile or ragweed family

Drug Interactions

Sedatives/benzodiazepinesmild

May have additive sedative effects

Blood thinnersmild

Chamomile family may have mild anticoagulant effects β€” may affect platelet aggregation or vitamin K-dependent clotting factors, altering anticoagulant efficacy

Possible Side Effects

Drowsinessuncommon

Tip: Take only before bed

Allergic reactionuncommon

Tip: Avoid if allergic to ragweed/chamomile

Warnings

  • Effects are subtle and gentle
  • Not a strong sedative like sleep medications
  • Limited direct human studies; mechanism-based recommendation

Top studies from 37+ peer-reviewed papers

meta-analysisn=1443
DOI

Liang H et al. β€’ Renal failure (2025)

β€œThrough rigorous experimental validation, our study demonstrates AS's significant clinical efficacy in managing DN.”
Key Findings:
  • Meanwhile, when the treatment duration exceeds 12 weeks, AS demonstrated a significant reduction in fasting blood glucose levels, indicating a time-dependent effect.
  • Through rigorous experimental validation, our study demonstrates AS's significant clinical efficacy in managing DN.
  • Specifically, AS has been shown to enhance renal function, ameliorate renal fibrosis, and positively influence iron metabolism.
  • Despite these promising outcomes, future research with a larger sample size must be conducted to further substantiate these findings.
systematic-review
DOI

Aktaş E et al. β€’ CNS neuroscience & therapeutics (2025)

β€œAlthough levodopa is indispensable for the symptomatic management of PD, emerging evidence supports the integration of plant-derived bioactive compounds as adjunct therapies with disease-modifying potential.”
Key Findings:
  • Although levodopa is indispensable for the symptomatic management of PD, emerging evidence supports the integration of plant-derived bioactive compounds as adjunct therapies with disease-modifying potential.
  • Future research should prioritize improving bioavailability, developing standardized formulations, and conducting long-term clinical trials to evaluate the translational applicability of these natural agents in Parkinson's disease therapy.
  • Further research warranted to confirm findings
meta-analysisn=12
DOI

Chang H et al. β€’ Nutrients (2018)

β€œConclusions: The present study suggested that high intake of flavonols (such as quercetin) may reduce the risk of colon cancer, and high intake of flavones (such as apigenin) may reduce the risk of rectal cancer.”
Key Findings:
  • High intake of dietary flavonols, flavones and anthocyanidins may decrease the risk of colorectal cancer; the pooled odds ratio (OR) for the highest intake compared with the lowest was 0.70 (0.54⁻0.90), 0.79 (0.83⁻0.99) and 0.78 (0.64⁻0.95), respectively.
  • No association between the intake of total flavonoids, flavanones or flavan-3-ols and the risk of colorectal cancer was observed.
  • Conclusions: The present study suggested that high intake of flavonols (such as quercetin) may reduce the risk of colon cancer, and high intake of flavones (such as apigenin) may reduce the risk of rectal cancer.
rctn=38408
DOI

Wang L et al. β€’ The American journal of clinical nutrition (2009)

β€œOur results do not support a major role of 5 common flavonols and flavones or selected flavonoid-rich foods in cancer prevention.”
Key Findings:
  • Our results do not support a major role of 5 common flavonols and flavones or selected flavonoid-rich foods in cancer prevention.
  • Published in The American journal of clinical nutrition (2009)
  • Further research warranted to confirm findings
systematic-review
DOI

Faysal M et al. β€’ Naunyn-Schmiedeberg's archives of pharmacology (2025)

β€œThe Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.”
Key Findings:
  • Flavonoids can enhance injury healing, reduce lesion size, and enhance synaptic plasticity and neurogenesis.
  • The full potential of flavonoids lies in their bioavailability, dose, and administration methods, but there are still challenges to overcome.
  • This review explores flavonoid-induced neuroprotection, its clinical implications, future research opportunities, and molecular mechanisms, highlighting the potential for innovative CNS injury therapies and improved patient health outcomes.Β© 2025.
  • The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
36
Total Studies
8.1/10
Avg Quality
10-66,940
Sample Size Range
1995-2025
Research Span

Study Type Distribution

Systematic Review
11
RCT
10
Meta-Analysis
8
In Vitro
3
Crossover
2
Review
1
Preclinical
1

This information is for educational purposes only and is not intended as medical advice. Always consult a qualified healthcare provider before starting any supplement.