Product Overview
Cardio Cytogen
Cardioactive peptides are endogenous regulators and emerging therapeutics in cardiovascular disease (CVD). Key chromogranin A (CgA)–derived peptides—catestatin, vasostatin, and chromofungin—are released from the sympathoadrenal system and myocardium and modulate cardiac contractility, vascular tone, and ischemia/reperfusion (I/R) tolerance.[1–3]
Mechanisms of Cardioprotection
- Catestatin & Vasostatin: Negative inotropic/lusitropic effects, feedback inhibition of catecholamine release, and protection from sympathetic overstimulation. Vasostatin can trigger preconditioning (pre-ischemia), while catestatin acts as a postconditioning agent (at reperfusion), engaging NO-dependent prosurvival signaling (PI3K/Akt → eNOS) via endothelium-dependent and direct myocardial actions; effects may be partly receptor-independent.[1,2]
- Chromofungin (CgA47–66): Induces negative inotropy through AKT/eNOS/cGMP/PKG and confers postconditioning cardioprotection (↓ infarct size, ↓ LDH) during I/R via PI3K, RISK cascade, mitoKATP channels, and miR-21.[3]
Cardiomyopeptides & Mitochondrial Protection
- Cardiomyopeptides (CMPs): Upregulate PPARγ, preserve mitochondrial integrity/respiration, and reduce myocardial injury and inflammation in I/R models (↓ AST, Mb, cTnT), limiting post-ischemic damage.[4]
Broader Peptide Therapeutics in CVD
- Atherosclerosis/Inflammation/Metabolism: ApoA-I/apoE mimetics, SOCS1-derived peptides, annexin-A1, and incretin mimetics target lipid transport, inflammation, and glucose-insulin tolerance.[5]
- Dietary/endogenous peptides: Animal/plant-derived peptides exhibit anti-inflammatory, antihypertensive, and anti-atherosclerotic activities, supporting nutrition-based prevention strategies.[6,7]
Targeting & Delivery
- Cardiac-Targeting Peptides (CTPs): Cell-penetrating/cardiac-homing sequences improve myocardial delivery and therapeutic index in preclinical models.[8]
Clinical & Translational Implications
- Endogenous/synthetic peptides (e.g., neuregulin-1, angiotensin-(1-9), growth/differentiation factors, IGF-1) are under evaluation for reducing cardiomyocyte death and preserving function post-injury.[9]
- Discovery across vertebrate/invertebrate systems highlights conserved peptidergic regulation of cardiac physiology and its translational relevance.[10]
Key Takeaways
- CgA-derived peptides (catestatin, vasostatin, chromofungin) counter I/R injury via NO-dependent and PI3K/Akt pathways and modulation of mitochondrial and ECM signaling.[1–3]
- CMPs bolster mitochondrial resilience and dampen myocardial injury/inflammation in I/R.[4]
- Therapeutic horizon: Targeted delivery and peptide/polypeptidomimetic design are expanding options for cardioprotection and remodeling.[5,8,9]
References
- Penna C, Tullio F, Perrelli MG, Mancardi D, Pagliaro P. Curr Med Chem. 2012;19(24):4074-85. doi:10.2174/092986712802429966.[1]
- Fornero S, Bassino E, Gallo MP, et al. Curr Med Chem. 2012;19(24):4059-67. doi:10.2174/092986712802429984.[2]
- Filice E, Pasqua T, Quintieri AM, et al. Peptides. 2015;71:40-48. doi:10.1016/j.peptides.2015.06.013.[3]
- Guo Z, Qian G, Pan X, et al. Int J Med Sci. 2025;22(1):44-52. doi:10.7150/ijms.102763.[4]
- Recio C, Maione F, Iqbal AJ, Mascolo N, De Feo V. Front Pharmacol. 2016;7:526. doi:10.3389/fphar.2016.00526.[5]
- Cam A, de Mejia EG. Mol Nutr Food Res. 2012;56(1):53-66. doi:10.1002/mnfr.201100535.[6]
- Li W, Lv M, Zhang T, et al. J Agric Food Chem. 2023;71(40):14562-14574. doi:10.1021/acs.jafc.3c02339.[7]
- Sahagun D, Zahid M. Biomolecules. 2023;13(12):1690. doi:10.3390/biom13121690.[8]
- Garrido V, Mendoza-Torres E, Riquelme JA, et al. Curr Pharm Des. 2017;23(18):2592-2615. doi:10.2174/1381612823666170112122637.[9]
- Schiemann R, Lammers K, Janz M, et al. Int J Mol Sci. 2018;20(1):E2. doi:10.3390/ijms20010002.[10]
All information provided is for research purposes only.
All COA’s available upon request: info@truformlabs.com
All information provided is for research purposes only.
Storage & Handling (Research Use)
- Lyophilized powder: Store sealed at −20 °C to −80 °C (desiccated, light-protected). For short term (≤2–3 weeks), 2–8 °C is acceptable.
- After reconstitution: Store at 2–8 °C and use within 7 days, or aliquot and freeze at −20 °C to −80 °C for ≤3 months.
- Handling: Prepare small aliquots to avoid freeze–thaw; keep on ice during prep; minimize air/light exposure.
- Vehicle & pH: Reconstitute per lot guidance (e.g., sterile saline/BWFI) near pH 7.0–7.4; avoid reactive metals/oxidants.
- Labeling: Record concentration, solvent, and prep date; follow lab SOPs and lot-specific stability notes.
All information provided is for research purposes only.