Snake Venom and Antivenom Pharmacology

  SNAKE VENOM & ANTIVENOM Chemistry, Composition, Mechanisms and Pharmacology Abstract This integrated teaching session for Phase III MBBS students focused on the pharmacology and toxicology of snake venom and the principles of antivenom therapy. The lecture covered the chemistry, composition, mechanisms of action, and pharmacological effects of snake venoms and antivenoms. Rational use of antivenoms, indications, administration protocols, adverse reactions, and supportive management strategies were discussed. The session also highlighted the translational importance of venom-derived compounds in modern drug development. Recent advances in antivenom research, including recombinant human monoclonal antibodies, toxin-specific inhibitors, synthetic antibody technologies, and next-generation broad-spectrum antivenoms, were reviewed. Current discoveries and emerging approaches aimed at improving efficacy, safety, affordability, and accessibility of antivenom therapy were also explor...

Lunatin-1: a membrane-disruptive peptide isolated from Hadruroides lunatus scorpion venom with cytotoxicity against MDA-MB-231 breast cancer cell line

 


Lunatin-1: a membrane-disruptive peptide isolated from Hadruroides lunatus scorpion venom with cytotoxicity against MDA-MB-231 breast cancer cell line

Abstract

Membrane-disrupting peptides - including antimicrobial and antitumor peptides - disrupt cell membrane through pore formation. Strategies for using these peptides as adjuvants in cancer treatment regimens have been investigated. In the context of a high recurrence rate and ineffective postoperative adjuvant chemotherapy treatment in triple-negative breast cancer (TNBC), the potential antitumor cytotoxic effect of Lunatin-1 was evaluated for the first time in the TNBC cell line MDA-MB-231. Synthetic Lunatin-1 was purified and its purity confirmed by mass spectrometry. Cytotoxicity of this peptide against MDA-MB-231 cells was associated with a rapid increase in propidium iodide-positive cells and LDH release through the loss of membrane integrity in a concentration and time-dependent manner. Staining with CellMask Deep Red to outline the cell membrane showed its disruption 5 min after Lunatin-1 treatment, which was not associated with necroptosis. Ultrastructural analysis by scanning electron microscopy showed membrane damage due to microvilli reduction and increased density of pores per cell compared to untreated cells. We concluded that Lunatin-1 is a membrane-disruptive peptide in this cellular model, highlighting it as an interesting tool for conjugating with cancer markers or anticancer drugs.
De Sousa Gomes, K., Raíssa-Oliveira, B., Schildknecht, S., De Lima, M. E., Melo-Braga, M. N., Gomes, D. A., De Castro Pimenta, A. M., Verano-Braga, T., Leist, M., & De Souza-Fagundes, E. M. (2025). Lunatin-1: A membrane-disruptive peptide isolated from Hadruroides lunatus scorpion venom with cytotoxicity against MDA-MB-231 breast cancer cell line. Biochimie. https://doi.org/10.1016/j.biochi.2025.06.006