toxins Article Neotropical Rattlesnake (Crotalus simus) Venom Pharmacokinetics in Lymph and Blood Using an Ovine Model Edgar Neri-Castro 1,2 , Melisa Bénard-Valle 1 , Dayanira Paniagua 3, Leslie V. Boyer 4, Lourival D. Possani 1 , Fernando López-Casillas 5, Alejandro Olvera 1, Camilo Romero 6, Fernando Zamudio 1 and Alejandro Alagón 1,* 1 Departamento de Medicina Molecular y Bioprocesos, Instituto de Biotecnologia, Universidad Nacional Autónoma de México, Av. Universidad 2001, Cuernavaca 62210, Mexico;
[email protected] (E.N.-C.);
[email protected] (M.B.-V.);
[email protected] (L.D.P.);
[email protected] (A.O.);
[email protected] (F.Z.) 2 Programa de Doctorado en Ciencias Biomédicas, Universidad Nacional Autónoma de México, Unidad de Posgrado, Edificio B Primer Piso, Ciudad Universitaria, Ciudad de México 04510, Mexico 3 Facultad de Ingeniería, Arquitectura y Diseño, Universidad Autónoma de Baja California, Ensenada, Baja California 22860, Mexico;
[email protected] 4 Venom Immunochemistry, Pharmacology, and Emergency Response (VIPER) Institute, University of Arizona,1501 N. Campbell Avenue, Tucson, AZ 85724, USA;
[email protected] 5 Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Ciudad Universitaria, Ciudad de México 04510, Mexico;
[email protected] 6 Centro Universitario UAEM Amecameca, Universidad Autónoma del Estado de México, Amecameca de Juárez 56900, Mexico;
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[email protected] Received: 15 June 2020; Accepted: 10 July 2020; Published: 17 July 2020 Abstract: The most abundant protein families in viper venoms are Snake Venom Metalloproteases (SVMPs), Snake Venom Serine Proteases (SVSPs) and Phospholipases (PLA2s). These are primarily responsible for the pathophysiology caused by the bite of pit-vipers; however, there are few studies that analyze the pharmacokinetics (PK) of whole venom (WV) and its protein families.