BPC-157 BioStrips

Product Information

Package contains 20 peptide buccal strips for in vitro research applications, each strip containing BPC-157 (300 mcg).

In research settings, BPC-157 has been studied primarily in animal models, where it has demonstrated potential cytoprotective, neuroprotective, and anti-inflammatory effects. It has shown promise in promoting the healing of various tissues, including skin, muscle, bone, ligaments, tendons, and the gastrointestinal tract.

BPC-157 appears to work through multiple mechanisms, including modulation of growth factors, nitric oxide pathways, and various cellular signaling processes involved in healing and regeneration.

Peptide Specifications

BPC-157 Research

BPC-157 is a promising peptide with diverse research applications in wound healing, musculoskeletal injuries, and cytoprotection. Its ability to promote angiogenesis and protect against vascular and epithelial damage highlights its potential for broader clinical research.

Wound Healing

BPC-157 promotes the formation of granulation tissue, angiogenesis, and collagen production, which are critical for wound healing. It has been shown to enhance vascular endothelial growth factor (VEGF) expression, which is crucial for new blood vessel formation.¹

The peptide enhances the proliferation and migration of endothelial cells and fibroblasts, which are essential for tissue repair. It activates pathways such as ERK1/2 and FAK-paxillin, which are involved in cell growth and migration.²

BPC-157 exhibits significant anti-inflammatory properties, which may contribute to its effectiveness in healing inflammatory skin lesions and other tissue injuries.³

BPC-157 has been effective in treating various skin injuries, including incisional/excisional wounds, deep burns, and diabetic ulcers. It accelerates wound closure and improves tissue remodeling and collagen deposition.⁴

Although the peptide’s healing mechanisms are partially understood, more research is needed to fully elucidate its pathways and interactions, particularly in complex wound healing scenarios.

Musculoskeletal Healing

BPC-157 has shown significant promise in enhancing tendon and ligament healing. It accelerates tendon fibroblast outgrowth, increases cell survival under stress, and promotes cell migration, likely through the activation of the FAK-paxillin pathway.⁵

BPC-157 enhances growth hormone receptor expression in tendon fibroblasts, which may potentiate the proliferation-promoting effects of growth hormone, contributing to tendon healing.⁶

The peptide has demonstrated efficacy in healing transected muscles and restoring myotendinous junctions in animal models. It counteracts muscle atrophy and promotes full functional recovery, as evidenced by improved biomechanical and functional assessments in treated rats.⁷

BPC-157 has also been shown to improve the healing of segmental bone defects in rabbits, comparable to traditional treatments like bone marrow or autologous cortical grafts.⁸

Angiogenesis

BPC-157 has been shown to promote angiogenesis through several mechanisms. It increases the expression and internalization of vascular endothelial growth factor receptor 2 (VEGFR2), which is crucial for angiogenic signaling. This activation leads to the stimulation of the VEGFR2-Akt-eNOS signaling pathway, enhancing endothelial tube formation and blood flow recovery in ischemic tissues.⁹ 

BPC-157 modulates the Src-Caveolin-1-eNOS pathway, promoting nitric oxide production and vasodilation, which are essential for vascular health and angiogenesis.¹⁰

BPC-157 has demonstrated significant angiogenic effects in various healing models. It enhances the healing of muscle and tendon injuries by up-regulating VEGF expression, which is vital for angiogenesis and tissue repair. ¹¹

Gastrointestinal Conditions

BPC-157 is known for its strong endothelial protection, which plays a crucial role in its ability to heal gastric and duodenal lesions. It effectively counteracts the damage induced by stress, cysteamine, and ethanol in experimental models, outperforming several standard treatments.¹²

BPC-157 has demonstrated significant protective effects against various GI injuries, including those caused by NSAIDs, alcohol, and stress. It stabilizes intestinal permeability and enhances cytoprotection, making it a promising candidate for mitigating NSAID-induced gastroenteropathy and leaky gut syndrome.¹³

The peptide has also shown efficacy in healing fistulas¹⁴ and promoting recovery in conditions like ulcerative colitis and multiple sclerosis.¹⁵

Ocular Health

BPC-157 has shown significant promise in treating glaucoma, particularly in models where episcleral veins are cauterized, leading to increased intraocular pressure. The peptide rapidly normalizes intraocular pressure and preserves the integrity of retinal ganglion cells and optic nerves. It achieves this by enhancing collateral pathways, which compensates for the occlusion of major vessels, thereby preventing glaucomatous damage.¹⁶

In cases of retinal ischemia induced by retrobulbar application of L-NAME, BPC-157 has been effective in counteracting the adverse effects. It restores normal blood vessel diameter and optic disc appearance, and maintains retinal thickness, thus preventing further ischemic damage. This effect is attributed to BPC-157’s interaction with the NO-system, which plays a crucial role in vascular health.¹⁷

BPC-157 has demonstrated efficacy in promoting corneal healing and maintaining transparency. It accelerates the healing of corneal epithelial defects and prevents neovascularization, which is crucial for preserving corneal clarity. This healing effect is observed in various models of corneal injury, including perforating corneal incisions.¹⁸

The peptide also shows potential in treating dry eye syndrome by counteracting the effects of lacrimal gland removal. BPC-157’s ability to heal ocular tissues and its established relationship with the NO-system suggest it could mitigate the symptoms of dry eye, which range from discomfort to severe visual impairment.¹⁹

References

1. Seiwerth, S., Sikiric, P., Grabarević, Ž., Zoričić, I., Hanževački, M., Ljubanović, D., Ćorić, V., Konjevoda, P., Petek, M., Ručman, R., Turković, B., Perović, D., Mikus, D., Jandrijević, S., Medvidović, M., Tadić, T., Romac, B., Kos, J., Perić, J., & Kolega, Z. (1997). BPC 157’s effect on healing. Journal of Physiology-Paris, 91, 173-178. https://doi.org/10.1016/S0928-4257(97)89480-6.
2. Huang, T., Zhang, K., Sun, L., Xue, X., Zhang, C., Shu, Z., Mu, N., Gu, J., Zhang, W., Wang, Y., Zhang, Y., & Zhang, W. (2015). Body protective compound-157 enhances alkali-burn wound healing in vivo and promotes proliferation, migration, and angiogenesis in vitro. Drug Design, Development and Therapy, 9, 2485 – 2499. https://doi.org/10.2147/DDDT.S82030.
3. Šola, M., Skroza, N., Mangino, G., Škrtić, A., Seiwerth, S., & Sikiric, P. (2022). Do We Have a New Psoriasis Drug?. The FASEB Journal, 36. https://doi.org/10.1096/fasebj.2022.36.s1.r5345.
4. Seiwerth, S., Milavić, M., Vukojević, J., Gojkovic, S., Krezic, I., Vuletić, L., Pavlov, K., Petrovic, A., Sikirić, S., Vraneš, H., Prtorić, A., Zizek, H., Durasin, T., Dobrić, I., Starešinić, M., Štrbe, S., Knežević, M., Šola, M., Kokot, A., Sever, M., Lovrić, E., Škrtić, A., Blagaic, A., & Sikiric, P. (2021). Stable Gastric Pentadecapeptide BPC 157 and Wound Healing. Frontiers in Pharmacology, 12. https://doi.org/10.3389/fphar.2021.627533.
5. Chang, C., Tsai, W., Lin, M., Hsu, Y., & Pang, J. (2011). The promoting effect of pentadecapeptide BPC 157 on tendon healing involves tendon outgrowth, cell survival, and cell migration.. Journal of applied physiology, 110 3, 774-80 . https://doi.org/10.1152/japplphysiol.00945.2010.
6. Chang, C., Tsai, W., Hsu, Y., & Pang, J. (2014). Pentadecapeptide BPC 157 Enhances the Growth Hormone Receptor Expression in Tendon Fibroblasts. Molecules, 19, 19066 – 19077. https://doi.org/10.3390/molecules191119066.
7. Japjec, M., Pavlov, K., Petrović, A., Starešinić, M., Šebečić, B., Buljan, M., Vraneš, H., Giljanovic, A., Drmic, D., Japjec, M., Prtorić, A., Lovrić, E., Vuletić, B., Dobrić, I., Blagaić, B., Škrtić, A., Seiwerth, S., & Predrag, S. (2021). Stable Gastric Pentadecapeptide BPC 157 as a Therapy for the Disable Myotendinous Junctions in Rats. Biomedicines, 9. https://doi.org/10.3390/biomedicines9111547.
8. Šebečić, B., Nikolić, V., Sikiric, P., Seiwerth, S., Šoša, T., Patrlj, L., Grabarević, Ž., Ručman, R., Petek, M., Konjevoda, P., Jadrijević, S., Perović, D., & Šlaj, M. (1999). Osteogenic effect of a gastric pentadecapeptide, BPC-157, on the healing of segmental bone defect in rabbits: a comparison with bone marrow and autologous cortical bone implantation.. Bone, 24 3, 195-202 . https://doi.org/10.1016/S8756-3282(98)00180-X.
9. Hsieh, M., Liu, H., Wang, C., Huang, H., Lin, Y., Ko, Y., Wang, J., Chang, V., & Pang, J. (2017). Therapeutic potential of pro-angiogenic BPC157 is associated with VEGFR2 activation and up-regulation. Journal of Molecular Medicine, 95, 323-333. https://doi.org/10.1007/s00109-016-1488-y.
10. Hsieh, M., Lee, C., Chueh, H., Chang, G., Huang, H., Lin, Y., & Pang, J. (2020). Modulatory effects of BPC 157 on vasomotor tone and the activation of Src-Caveolin-1-endothelial nitric oxide synthase pathway. Scientific Reports, 10. https://doi.org/10.1038/s41598-020-74022-y.
11. Brčić, L., Brčić, I., Starešinić, M., Novinščak, T., Sikiric, P., & Seiwerth, S. (2009). Modulatory effect of gastric pentadecapeptide BPC 157 on angiogenesis in muscle and tendon healing.. Journal of physiology and pharmacology : an official journal of the Polish Physiological Society, 60 Suppl 7, 191-6 . https://doi.org/10.1135/CSS200911118.
12. Sikiric, P., Seiwerth, S., Grabarević, Ž., Petek, M., Ručman, R., Turković, B., Rotkvić, I., Jagić, V., Duvnjak, M., Miše, S., Djačić, S., Šeparović, J., Veljača, M., Sallmani, A., Banic, M., & Brkić, T. (1994). The beneficial effect of BPC 157, a 15 amino acid peptide BPC fragment, on gastric and duodenal lesions induced by restraint stress, cysteamine and 96% ethanol in rats. A comparative study with H2 receptor antagonists, dopamine promotors and gut peptides.. Life sciences, 54 5, PL63-8 . https://doi.org/10.1016/0024-3205(94)00796-9.
13. Park, J., Lee, H., Sikiric, P., & Hahm, K. (2020). BPC157 rescued NSAID-cytotoxicity via stabilizing intestinal permeability and enhancing cytoprotection.. Current pharmaceutical design. https://doi.org/10.2174/1381612826666200523180301.
14. Sikiric, P., Drmic, D., Sever, M., Klicek, R., Blagaic, A., Tvrdeić, A., Kralj, T., Kovac, K., Vukojević, J., Siroglavić, M., Gojkovic, S., Krezic, I., Pavlov, K., Rasic, D., Mirkovic, I., Kokot, A., Škrtić, A., & Seiwerth, S. (2020). Fistulas healing. Stable gastric pentadecapeptide BPC 157 therapy.. Current pharmaceutical design. https://doi.org/10.2174/1381612826666200424180139.
15. Sikiric, P., Seiwerth, S., Ručman, R., Turković, B., Rokotov, D., Brčić, L., Sever, M., Klicek, R., Radić, B., Drmic, D., Ilić, S., Kolenc, D., Stambolija, V., Zoričić, Z., Vrčić, H., & Šebečić, B. (2012). Focus on ulcerative colitis: stable gastric pentadecapeptide BPC 157.. Current medicinal chemistry, 19 1, 126-32 . https://doi.org/10.2174/092986712803414015.
16. Sikiric, P., Kokot, A., Kralj, T., Zlatar, M., Masnec, S., Lazić, R., Lončarić, K., Oroz, K., Sablić, M., Boljesic, M., Antunović, M., Sikirić, S., Štrbe, S., Stambolija, V., Orešković, B., Kavelj, I., Novosel, L., Zubcic, S., Krezic, I., Škrtić, A., Jurjević, I., Blagaić, B., Seiwerth, S., & Starešinić, M. (2023). Stable Gastric Pentadecapeptide BPC 157—Possible Novel Therapy of Glaucoma and Other Ocular Conditions. Pharmaceuticals, 16. https://doi.org/10.3390/ph16071052.
17. Zlatar, M., Kokot, A., Vuletić, L., Masnec, S., Kralj, T., Periša, M., Barišić, I., Radić, B., Milanović, K., Drmic, D., Seiwerth, S., & Sikiric, P. (2021). BPC 157 as a Therapy for Retinal Ischemia Induced by Retrobulbar Application of L-NAME in Rats. Frontiers in Pharmacology, 12. https://doi.org/10.3389/fphar.2021.632295.
18. Masnec, S., Kokot, A., Zlatar, M., Kalauz, M., Radić, B., Klicek, R., Drmic, D., Lazić, R., Seiwerth, S., & Sikiric, P. (2015). Perforating Corneal Injury in Rat and Pentadecapeptide BPC 157. The FASEB Journal, 29. https://doi.org/10.1016/j.exer.2015.04.016.
19. Radevski, F., Peraic, P., Mašek, T., Starčević, K., Krezic, I., Pavlov, K., Drmic, D., Kralj, T., Seiwerth, S., Sikiric, P., & Kokot, A. (2019). Stable Gastric Pentadecapeptide BPC 157 in Rats Subjected to High Fructose (80%) Diet for One Month Counteracts Hypertension and Compromised Optic Disc Head Circulation and Following Atrophy. The FASEB Journal, 33. https://doi.org/10.1096/fasebj.2019.33.1_supplement.822.9.