Great part of the veterinary care in wild carnivores is intended to treat the dental disorders, and oral cavity disorders may generally affect the animal health as a whole. It is factual that knowing the location of the mandibular foramen is vital for local anesthetic block of the inferior alveolar nerve, however, there is still no data on the morphometry of the hoary fox mandibular foramen. The aim was describing morphometry of the mandibular foramen of this species and associating its position with anatomic reference points in the mandible, thus providing support for more effective local anesthetic block of the inferior alveolar nerve in such species. Four adult jaws of Lycalopex vetulus were used. Radiography and biometrics of the hemimandibulas were performed. The rostral third of the jaw body in a lateral view presented three mental foramens, being a rostral, a medium and a caudal. Each hemimandibula presented I3/C1/PM4/M3. The angle of the mandible was marked by the masseteric fossa, the angular incisure, the angular process and the mandibular foramen, and this last one located perpendicularly to the dorsal edge of the angular incisures in medial view. In this view, the crevice to the milohyoid nerve, projected in the caudodorso rostral direction, was also evidenced. The ramus of the mandible was characterized by the presence of the condylar and coronoid processes, and by the dorsal and ventral mandibular incisions. Statistical analyzes did not present significant differences between the antimeres of the studied animals, and the penetration of the needle perpendicularly to the dorsal end of the angular incision on average 8.79mm, overlapped to the medial face of the angle of the mandible could be indicated. Alternatively, the access may also be achieved by inserting the needle in an average of 17.69mm perpendicular to the dorsal end of the angular process, in contact with the medial aspect of the angle of the mandible, and in caudo-rostral projection, also allowing a better anesthetic blockade of the inferior alveolar nerve in L. vetulus. It can also be concluded that the masseteric fossa, the dorsal and ventral mandibular angles, the crevice to the milohyoid nerve, the ramus of the mandible and the mandibular foramen presented differences in their topographic descriptions when compared to the other canids.

Henrique Inhauser Riceti Magalhães, Jeferson Borges Barcelos, Fabiano Braz Romão, Tânia Ribeiro Junqueira Borges, Roseâmely Angélica de Carvalho-Barros, Maria Angelica Miglino, Frederico Ozanam Carneiro e Silva, Lucas de Assis Ribeiro. Anat Cell Biol 2021;54:202-11. https://doi.org/10.5115/acb.20.301

Boars kept on commercial farms use their canine teeth as a mechanism of defense and attack in order to express their natural instincts, which could result in fractures of the teeth and jaws. Thus, utilizing local desensitization of the inferior alveolar nerve is crucial for executing therapeutic procedures in the oral cavities of those animals. Then, the goal is to carry out the morphometry of the mandibular foramen of that species, correlating it with the mandibular structures, while doing so in the safest manner for the animals. For that purpose, six hemimandibles of young-aged Sus scrofa scrofa were used, from which the proposed measurements were taken. On average, the lateral margin of the condylar process stood 142.43 mm away from the root of the lower medial incisive tooth. The longitudinal axis of the body of the mandible measured 22.3 mm at the level of the diastema that exists between the fourth lower premolar tooth and the first lower molar tooth. The mandibular foramen, from the caudal limit of the ventral margin, would be positioned at26.6 mm from the ventral margin of the angle of the mandible in that level, 34.92 mm away from the medial margin of the condylar process, and 38.63 mm away from the dorsal limit from the caudal margin of the coronoid process. The lack of statistically significant differences, and observing that the osseous accident under scrutiny had been positioned in the ramus of the mandible, indicated that the proposed procedure should be performed from the introduction of the needle in an oblique and rostrodorsal direction for 2.0 cm, and angulated at 60º with the anatomic reference created by the medial demarcation obtained via the support of the thumb on the lateral margin of the ramus of the mandible, ventrally to the zygomatic arch, all while preserving neighboring structures and establishing an unheard-of anesthetic methodology for boars.

Bovine spongiform encephalopathy (BSE) is a fatal transmissible spongiform encephalopathy caused by the misfolding of the host prion protein (PrP), representing a unique intersection between molecular pathology, neuroanatomy, and public health regulation. Although historically framed as a single feedborne epizootic, BSE is now recognized as a spectrum of strain-defined prion disorders encompassing classical and atypical forms with distinct origins, neuroanatomical trajectories, and surveillance implications. This review integrates advances in prion biology, neurodegenerative mechanisms, and anatomical pathways of neuroinvasion to reframe BSE as a heterogeneous disease entity. We synthesize evidence on PrP^C structure, trafficking, and proteolytic processing to explain how normal cellular physiology enables strain-specific conversion to pathogenic PrP^Sc and subsequent neurotoxicity. Distinct patterns of neuroinvasion and regional vulnerability are discussed for classical versus atypical (H- and L-type) BSE, highlighting differences in lymphoid involvement, brainstem targeting, and cortical or cerebellar tropism. We further examine how these biological differences translate into diagnostic sensitivity, surveillance design, and zoonotic risk assessment. By integrating molecular strain diversity with neuroanatomical connectivity, this review underscores the limitations of obex-centered surveillance for atypical BSE and emphasizes the need for proportionate yet precautionary monitoring strategies. These considerations should be interpreted in light of surveillance-dependent detection biases, which influence the apparent distribution of BSE forms. Ultimately, BSE emerges as a critical model for understanding how protein misfolding disorders bridge cellular mechanisms, animal health, and human public health policy.

This work aimed to describe the origin, distribution, and ramifications of the ischiadicus nerve in the giant anteater and to provide anatomical data which could explain not only the evolutionary aspects but also provide important information for other related works. For the present study, four specimens were used, prepared by perfusion of 10% formaldehyde solution via the femoral artery, for conservation and dissection. The origin of the right and left ischiadicus nerves in the giant anteater from the ventral ramification of the third lumbar (L3) and the first (S1), second (S2), and third (S3) sacral spinal nerves. These nerves were symmetrical in all animals studied. The distribution and ramification occurred to the superficial, middle, and deep gluteal, gemelli, piriform, quadratus femoris, tensor fasciae latae, caudal crural abductor, cranial and caudal parts of the biceps femoris, adductor, semitendinous, and cranial and caudal parts of the semimembranous muscles. Based on the origins of the ischiadicus nerves, there is a caudal migration in the nerve location in animals in a more recent position on the evolutionary scale due to reconfiguration of the lumbosacral plexus, resulting from the increase in a number of lumbar vertebrae. There is no complete homology of the muscle innervation.