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Total Glucosides of Paeony (TGP)

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Specifically for Sjogren’s Syndrome

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Why it works for Sjogren’s Syndrome:

pSS is driven by dysregulated innate/adaptive immunity (e.g., activated dendritic cells; polarized Th1/Th17 responses) that damages exocrine glands. TGP is a standardized extract (rich in paeoniflorin) with immunomodulatory effects that map onto these pathways:

  • Dendritic cell “cool-down” – TGP can blunt dendritic-cell maturation by blocking TLR4/5-NF-κB signaling, which downstream reduces pro-inflammatory cytokines and helps de-activate T-cell responses. ScienceDirect
  • T-cell rebalancing (↓Th1/Th17) and broader anti-inflammatory activity attributed to paeoniflorin/TGP; several reviews and mechanistic studies document effects across JAK/STAT, NF-κB, MAPK, and PI3K/AKT/mTOR pathways. ScienceDirect
  • Secretory function & symptoms – In clinical testing, TGP improved patient-reported dryness/fatigue scores and some tear/saliva measures (see RCT evidence below). SpringerLink

How to use for Sjogren’s Syndrome:

The most rigorous dosing information comes from a multicentre, double-blind RCT in pSS:

  • Dose: 600 mg three times daily (TID) oral TGP (total 1,800 mg/day).
  • Duration: 24 weeks.
  • Assessments: patient-reported ESSPRI; dryness/fatigue VAS; Schirmer’s test; salivary flow; ESR; routine safety labs. SpringerLink

Other clinical programs in autoimmune diseases also use ~1,800 mg/day orally, supporting this ballpark as a studied human dose. SpringerLink

Combination therapy: Small RCTs and meta-analyses (mostly from China) have evaluated TGP + hydroxychloroquine (HCQ) versus HCQ alone in pSS, reporting incremental symptom benefits; quality varies but the signal favors combination in some outcomes. Discuss combinations with your rheumatologist if you’re already on HCQ. Directory of Open Access Journals

Monitoring used in studies / sensible in practice

  • Baseline and periodic CBC, LFTs (ALT/AST), renal function, and disease scores (e.g., ESSPRI/ESSDAI). SpringerLink
  • Re-assess at 12–24 weeks to decide on continuation (onset can be gradual). Frontiers

Scientific Evidence for Sjogren’s Syndrome:

Phase III-style RCT (China): 320 adults with pSS randomized 2:1 to TGP 600 mg TID vs placebo for 24 weeks.

Results: Greater improvement in ESSPRI; better scores for dryness (eyes/throat/vagina), fatigue, patient global, Schirmer’s test, and ESR; stimulated salivary flow improved at week 12 (not sustained at week 24). AEs ~10.9% and generally mild. SpringerLink

Randomized, double-blind pilot (45 pts, 24 weeks): Showed clinical and immunologic improvements with TGP vs placebo. (Full text is behind a paywall, but abstract and congress reports are accessible.) Annals of the Rheumatic Diseases

Systematic review & meta-analysis (2019, Frontiers in Pharmacology): Pooled Chinese RCTs of TGP (alone or add-on) in pSS; favored symptom and some objective improvements with acceptable safety, while calling for larger, higher-quality multinational trials. Frontiers

Recent mechanistic/experimental updates (2024–2025): Preclinical work continues to show TGP/paeoniflorin modulates Th subsets and glandular inflammation in SS models, providing biologic plausibility. Clinical and Experimental Rheumatology

Specific Warnings for Sjogren’s Syndrome:

1) Regulatory status & availability

  • TGP is approved in China (since 1998) as a disease-modifying drug for rheumatoid arthritis; its use in pSS is off-label even in China and not approved by regulators such as the TGA (Australia), FDA (US), or EMA (EU). BMJ Open

2) Guideline position

  • Contemporary EULAR guidance for Sjögren’s does not include TGP among recommended systemic therapies; evidence is geographically limited and not yet integrated into Western guidelines. Annals of the Rheumatic Diseases

3) Adverse effects seen in trials / reports

  • Overall AE rates in pSS RCTs were modest (≈10–11% with TGP over 24 weeks), typically GI upset (nausea, diarrhea), mild dizziness/headache, or transient LFT elevations; severe events were uncommon. Always monitor labs, particularly if you have liver disease or take other hepatotoxic drugs. SpringerLink
  • Broader safety syntheses (mostly RA populations) suggest TGP is generally well-tolerated and may even mitigate MTX/LEF hepatotoxicity in combinations—useful if you’re on those agents for overlap arthritis—but individual monitoring still applies. BioMed Central

4) Drug interactions and special populations

  • Robust interaction data are limited. Given immunomodulatory effects, coordinate with your rheumatologist if you’re on immunosuppressants/biologics. (Most combination data come from Chinese studies with HCQ or csDMARDs.) Directory of Open Access Journals
  • Pregnancy/breastfeeding: There’s insufficient human data specific to TGP; defer use unless your specialist feels benefits clearly outweigh risks. (When evidence is sparse, standard perinatal medicines guidance is to avoid non-essential agents.) GOV.UK
  • Quality control: Because TGP is a botanical extract, ensure pharmaceutical-grade product and physician oversight—especially outside China, where formulations/standards may vary. Background pharmacology reviews describe its composition (paeoniflorin-rich) and standardization issues. Frontiers

General Information (All Ailments)

Note: You are viewing ailment-specific information above. This section shows the general remedy information for all conditions.

What It Is

Total Glucosides of Paeony (TGP) is a standardized extract from the root of Paeonia lactiflora (white peony), a traditional medicinal plant widely used in Chinese medicine. The main active constituent is paeoniflorin, together with minor related glycosides (e.g., albiflorin). TGP is available as a regulated oral botanical drug in China, commonly used in chronic autoimmune and inflammatory disorders.

How It Works

TGP is not a simple anti-inflammatory like NSAIDs; its actions are immune-modulatory and tissue-protective. Modern pharmacology attributes its clinical effects to:

  • Immunoregulation: Down-regulates overactive Th1/Th17/Tfh pathways and inflammatory cytokines (e.g. TNF-α, IL-6), while promoting regulatory T-cell activity. This shifts the immune response from attack to tolerance.
  • Endothelial and microcirculation protection: Improves microvascular blood flow and reduces endothelial injury — helpful in autoimmune vasculopathy.
  • Antioxidant and anti-fibrotic effects: Reduces oxidative stress and pathways that drive tissue scarring, relevant in chronic immune-mediated organ damage.
  • Gut–immune axis effects: Evidence suggests TGP reshapes gut microbiota composition in ways that correlate with reduced autoimmune activity.

In clinical practice it is often used for systemic lupus erythematosus, rheumatoid arthritis, Sjögren’s syndrome, liver immune disease, and other inflammatory conditions — frequently in combination with basic therapy to improve tolerability and reduce steroid burden.

Why It’s Important

  • Steroid-sparing potential: Enables dose reduction of glucocorticoids or immunosuppressants in some patients, reducing long-term toxicity.
  • Long-term safety profile superior to most immunosuppressives: Fewer serious infections, less metabolic disruption, and no bone-marrow suppression in typical use.
  • Bridges traditional and modern care: Offers an evidence-supported botanical option in immune disease that is mechanistically rational rather than purely “herbal folklore”.
  • Useful in chronic diseases requiring modulation, not blunt suppression: Autoimmunity requires durable re-balancing, and TGP acts on the immune “thermostat,” not only the “fire.”

Considerations

  • Evidence is largely from Chinese trials: Many are high-volume but heterogeneous; global Phase III-level data are more limited. Extrapolation should be cautious.
  • Regulatory status differs by country: In China, TGP is a prescription drug; elsewhere it may be sold as a supplement with variable quality control. Standardization matters — effects are dose and purity dependent.
  • Onset is gradual: Clinical benefit is typically seen over weeks to months, not days; it is not a rescue medication.
  • Drug interactions and combined protocols: Usually compatible with DMARDs and low-dose steroids, but immunomodulation can interact with vaccination timing and infection risk assessments.
  • Contraints in specific populations: Use in pregnancy, severe organ failure, or active infection should be individualized. Elevated bleeding risk has been occasionally reported, so peri-operative use should be reviewed.
  • Quality and adulteration risk outside formal drug channels: Poor-grade “peony extracts” in supplement markets may not reflect therapeutic TGP. Clinically relevant dosing and consistent paeoniflorin content require vetted supply.

Helps with these conditions

Total Glucosides of Paeony (TGP) is most effective for general wellness support with emerging research . The effectiveness varies by condition based on clinical evidence and user experiences.

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pSS is driven by dysregulated innate/adaptive immunity (e.g., activated dendritic cells; polarized Th1/Th17 responses) that damages exocrine glands. T...

0 votes Updated 1 month ago 4 studies cited

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