Environ Monit Assess. 2025 Nov 2;197(12):1288. doi: 10.1007/s10661-025-14752-6.
ABSTRACT
Global human population growth results in increased emissions of chemical pollutants like heavy metals such as cadmium (Cd) and lead (Pb). These two non-essential elements have strong bioavailability and toxicity, causing harmful health effects on humans, and the wider environment. Synanthropic wildlife species like the white-eared opossum may act as sentinels of environmental contamination, since they have a high incidence in urban areas and close contact with humans. The aim of this study was to conduct toxicological and histopathological analyses of white-eared opossums (Didelphis albiventris) that live in the city of Campo Grande, capital of Mato Grosso do Sul state in Brazil. In addition, we surveyed Cd and Pb in soil and water from sites where D. albiventris were captured. A total of 23 animals were captured and, after recording biological parameters, were euthanized and necropsied. Liver and central nervous system (CNS) samples were sent for toxicological analysis of Cd and Pb. Fragments of the liver, brain, kidney, and reproductive system were collected for histopathological evaluation. The presence of Cd and Pb in the liver and CNS was identified, with a high concentration of Pb in the CNS. Additionally, we found higher concentrations of Pb in both soil and water samples than in the animals. In the histopathological analysis, mild to moderate degenerative tissues lesions were found and may be compatible with damage caused by the presence of Cd and Pb. Nevertheless, our statistical analysis indicated that contamination by Cd and Pb did not threaten the health of the sampled animals. This study is the first in Brazil to detect background levels of Cd and Pb in the liver and CNS of D. albiventris, correlating these concentrations with histopathological lesions. The findings further emphasize the importance of understanding the interactions among the environment, humans, wildlife, and domestic animals within the One Health framework.
PMID:41177812 | DOI:10.1007/s10661-025-14752-6