B7-33

Also known as: Relaxin-2 Analog

Overview

B7-33 is a peptide that mimics the natural hormone relaxin-2, helping reduce scarring (fibrosis) and inflammation, while supporting heart and tissue health. B7-33 is a synthetic peptide derived from human relaxin-2, engineered to selectively activate the relaxin receptor (RXFP1). This peptide retains the anti-fibrotic, anti-inflammatory, and cardioprotective effects of relaxin-2 while minimizing vasodilatory side effects. It works by improving blood flow, breaking down excess collagen, and promoting tissue healing, making it a potential treatment for conditions like heart or lung fibrosis and chronic inflammation. B7-33 demonstrates significant potential in treating fibrotic diseases, improving cardiac function, and promoting tissue repair and regeneration.

Benefits

- Reduces viral binding sites

- Treats pulmonary, cardiac, and hepatic fibrosis

- Reduces blood pressure and supports heart health

- Reduces chronic inflammation

- Mitigates pulmonary hypertension

- Enhances tissue repair and vascularization

Consider This Peptide If You Want To

- Reduce fibrosis (scarring) and inflammation, especially in conditions affecting the heart, lungs, or other tissues

- Seek cardiovascular or tissue repair support, particularly for improving blood flow and reducing excess collagen buildup

Dosage & Administration

Dosage Guidelines

Recommended Dosage

• Amount: 250 mcg

• Frequency: daily

• Duration: 1 week

• Rest Period: 1 week

• Time of Day: morning

• Ingestion: subcutaneous

Administration Routes:

- Subcutaneous

Research Findings on Dosage:

1. Subcutaneous injection:

• Commonly Reported Dosage: 250 mcg/kg twice daily

• Duration: 7-14 days in clinical trials, but more investigation is needed

Mechanism of Action

How this peptide works in the body

RXFP1 Activation:

• B7-33 selectively binds to the relaxin family peptide receptor 1 (RXFP1), activating the cyclic AMP-protein kinase A (cAMP-PKA) signaling pathway. This activation reduces fibrosis, improves endothelial function, and enhances vascular relaxation, leading to better blood flow and reduced tissue stiffness in the heart, lungs, and other organs.

AT2R Activation:

• By interacting with the angiotensin II receptor type 2 (AT2R), B7-33 counteracts the effects of angiotensin II, which helps lower blood pressure and inflammation. This pathway also reduces ACE2 receptor transcription, potentially limiting viral entry in conditions like COVID-19-associated lung injury.

Anti-Fibrotic Effects:

• B7-33 inhibits collagen deposition by activating matrix metalloproteinases (MMPs), enzymes responsible for breaking down excess extracellular matrix proteins. This effect prevents scarring and fibrosis progression in tissues like the heart, liver, and lungs, making it a promising treatment for fibrotic diseases.

Anti-Inflammatory Action:

• B7-33 reduces the expression of pro-inflammatory cytokines such as TNF-α and IL-6 while upregulating elastin synthesis and vascular remodeling proteins. This leads to lower systemic inflammation and improved tissue elasticity, benefiting conditions like pulmonary hypertension and chronic inflammation.

Cardiovascular Protection:

• By enhancing myocardial relaxation and reducing systemic vascular resistance, B7-33 improves cardiac output and protects against heart failure. It also supports pulmonary circulation by reducing pulmonary artery pressure, making it beneficial for vascular diseases and hypertension.

Tissue Regeneration:

• B7-33 stimulates angiogenesis by upregulating vascular endothelial growth factor (VEGF), improving endothelial cell function, and accelerating wound healing and organ repair. This promotes better oxygen delivery and faster recovery from tissue damage.

Side Effects & Cautions

Common Side Effects

- Localized injection site reactions are possible

Rare Side Effects

- Long-term effects in humans remain under study

Research & References

Research Highlights

1. Anti-Fibrotic Effects in Cardiac Fibrosis (2017): Demonstrated reduced fibrosis and improved heart function in animal models.

2. Lung Fibrosis Studies (2020): Highlighted the ability of B7-33 to inhibit excessive collagen production in pulmonary tissue.

3. Wound Healing and Angiogenesis: Shown to promote blood vessel formation and tissue repair in preclinical studies.

References

• B7-33 as a Novel Anti-Fibrotic Therapy (2017): Demonstrated efficacy in reducing cardiac fibrosis and inflammation

• Relaxin Derivatives and Tissue Repair (2020): Explored the role of RXFP1 activation in promoting tissue regeneration

• Therapeutic Potential of Relaxin Mimetics: Summarized applications of relaxin-based peptides in treating fibrotic diseases