During 2017-2018, a survey for the rat lungworm, (Nematoda: Metastrongyloidea), in rodents from Piedmont and Lower Coastal Plains physiographic regions of Georgia was conducted. On 4 occasions, a single worm was recovered from the pulmonary vessels of a single cotton rat (). One of these worms was identified as a sp. and the remaining 3 as a sp. by morphology. No were found. (Nematoda: Physalopteroidea) and species (Nematoda: Spiruroidea) are stomach parasites of many wild and domestic animals. This is the first report of these species in the pulmonary vessels of a definitive host. To better characterize these parasites, representative specimens were collected from cotton rat stomachs and identified morphologically and molecularly. Based on partial cytochrome oxidase subunit 1 () gene sequences, from stomachs were identical to the sp. from the pulmonary vessels. The sequences from the sp. from the stomach exhibited a higher degree of variability but confirmed that the pulmonary worms were the same species. Furthermore, sequences of from a coastal site clustered separately from a clade of sequences from cotton rats from a Piedmont site. Our data show that adult worms recovered from pulmonary vessels of cotton rats could be either or sp., indicating that these parasitic worms are not always restricted to the stomach and that worms from pulmonary vessels must be carefully examined to obtain a definitive diagnosis of infection.
Download full-text PDF |
Source |
---|
Future Cardiol
January 2025
Department of Cardiovascular Disease, Baylor Scott and White Medical Center - Temple, TX, USA.
Approximately 5-10% of patients with hypertension have secondary hypertension. We describe a case of secondary hypertension from bilateral renal artery stenosis (RAS): "Pickering syndrome." This is a case of hypertension secondary to bilateral RAS which provides an opportunity to review secondary hypertension with a specific focus on RAS, in terms of when to consider work up, causes of secondary hypertension, diagnostic testing, and treatment.
View Article and Find Full Text PDFJ Vet Intern Med
January 2025
Department of Veterinary Sciences, University of Pisa, Pisa, Italy.
Background: Evaluating the size of the pulmonary artery (PA) is key for the echocardiographic assessment of pulmonary hypertension (PH) in dogs.
Hypothesis/objectives: To compare the diagnostic accuracy of the main PA (MPA) and right PA (RPA) sizes for the echocardiographic detection of PH in dogs, and to evaluate differences between precapillary and postcapillary PH dogs.
Animals: Four hundred four dogs; 136 controls and 268 with PH.
NeuroSci
January 2025
Department of Neurophysiology, Neuropsychology and Neuroinformatics, Medical University of Gdansk, 80-210 Gdansk, Poland.
This review emphasises the importance of the cardiovascular response to facial cooling (FC) and breath holding in both sexes. The trigemino-cardiac reflex, triggered by FC, reduces heart rate (HR) and constricts blood vessels. When combined with breath holding, this effect intensifies, enhancing the cardiodepressive impact.
View Article and Find Full Text PDFPulm Circ
January 2025
Department of Imaging and Pathology, Biomedical MRI KU Leuven Leuven Belgium.
The pulmonary vasculature plays a pivotal role in the development and progress of chronic lung diseases. Due to limitations of conventional two-dimensional histological methods, the complexity and the detailed anatomy of the lung blood circulation might be overlooked. In this study, we demonstrate the practical use of optical serial block face imaging (SBFI), ex vivo microcomputed tomography (micro-CT), and nondestructive optical tomography for visualization and quantification of the pulmonary circulation's 3D architecture from macro- to micro-structural levels in murine lung samples.
View Article and Find Full Text PDFBreathe (Sheff)
January 2025
Université Paris-Saclay, INSERM UMR_S 999, Hypertension Pulmonaire: Physiopathologie et Innovation Thérapeutique (HPPIT), Faculté de Médecine, Le Kremlin-Bicêtre, France.
Pulmonary arterial hypertension (PAH) is a severe disorder of the pulmonary vasculature leading to right ventricular failure. This pulmonary vascular remodelling leads to increased pulmonary vascular resistance and high pulmonary arterial pressures. Despite the development of new therapies, many patients continue to experience significant morbidity and mortality.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!