First documented cases of invertebrate predation by greater grisons (Galictis vittata)

  First documented cases of invertebrate predation by greater grisons (Galictis vittata) Abstract  We report the first documented predation of invertebrates by greater grisons (Galictis vittata) based on camera-trap footage from a mineral lick in Southeastern Peru. Two adult individuals were recorded capturing and consuming large arachnids, likely whip spiders (Amblypygi), from a natural cavity. One grison visibly removed and discarded part of the prey prior to ingestion, suggesting selective handling to reduce risk from defensive structures. These observations extend the known cavity-focused foraging behavior of G. vittata and indicate that amblypygids may represent an underreported but regular prey item in tropical habitats. Pottie, Sam, y Adrian Forsyth. 2026. «Primeros Registros Documentados De depredación De Invertebrados Por El grisón (Galictis Vittata)». Mammalogy Notes 12 (2), 608. https://doi.org/10.47603/mano.v12n2.608 .

Can Scorpion Venom Peptides Be Safely Used in Cardiovascular Therapy: A Systematic Review

 

Image Credit: Luis A. Roque, Arácnido Taxonomy

Can Scorpion Venom Peptides Be Safely Used in Cardiovascular Therapy: A Systematic Review

Abstract

Scorpion venom contains numerous bioactive peptides with potent cardiovascular effects, including bradykinin-potentiating peptides (BPPs), ion channel modulators, and cardioprotective molecules. These peptides show promise for conditions such as hypertension, cardiac injury, and arrhythmias. However, concerns regarding toxicity, immunogenicity, and off-target actions have limited their clinical development. This systematic review evaluates the therapeutic potential and safety of scorpion venom peptides for cardiovascular applications. A systematic search of PubMed, Scopus, Google Scholar, and Semantic Scholar identified 1,141 articles. Screening of 463 abstracts and full-text review of 446 eligible studies resulted in 17 publications meeting the inclusion criteria. Extracted data included mechanisms, efficacy, toxicity, and translational challenges. BPPs consistently demonstrated ACE inhibition, B2 receptor activation, and significant antihypertensive effects in animal models. Several peptides also showed cardioprotective activities by reducing oxidative stress, inflammation, and apoptosis. Ion channel-active peptides influenced cardiac electrophysiology, but many showed proarrhythmic risks due to hERG potassium channel blockade or interactions with Nav1.4/1.5 sodium channels. Structure-activity modification studies improved specificity and reduced toxicity in selected variants. Despite encouraging preclinical data, no scorpion venom peptide has progressed to clinical trials for cardiovascular indications. Major barriers include immunogenicity, instability, delivery challenges, and safety concerns. Scorpion venom peptides represent promising leads for novel cardiovascular therapeutics, particularly as antihypertensive and cardioprotective agents. However, significant toxicological and translational limitations remain. Advances in peptide engineering, targeted delivery, and clinical evaluation are crucial for safely harnessing their therapeutic potential.

Binorkar S V, Sawant R, Ukey R N, et al. (March 24, 2026) Can Scorpion Venom Peptides Be Safely Used in Cardiovascular Therapy: A Systematic Review. Cureus 18(3): e105747. doi:10.7759/cureus.105747