Induction of sperm impairments in mice as a sensitive biomarker of arsenic toxicity

The ubiquitous presence of arsenic (a toxic metalloid) in our environment, particularly in our drinking water, is a serious health hazard of global concern. The present work deals with the assessment of arsenic toxicity through the analysis of induced sperm impairments in sperm head morphology and sperm count in mice at low exposures compared to the magnitude of response at high exposure levels. The animals were exposed to four doses of arsenic, ranging from lowest dose of 0.3 μg kg^?1 day^?1 (the human reference dose) to higher dose of 30 μg kg^?1 day^?1 for 15 consecutive days. The epididymal sperms were harvested after one spermatogenic cycle on the 36th day and were scored for the presence of any abnormality in their head morphology as well as changes in their count. Exposure to arsenic significantly induced, in a dose-dependent manner, increases in the frequency of sperms with abnormal head morphology from 5.12 % in control to 9.23 % in lowest dose group and 23.02 % in highest dose group. In contrast, the mean sperm counts in the epididymal wash were decreased from 6.05 million per milliliter in the control to 4.95 million per milliliter in the lowest dose group and 3.07 million in the highest dose group. The analysis of sperm impairments in mice was, therefore, found to be a highly sensitive assay to assess arsenic toxicity, exhibiting a marked male reprotoxic effect of arsenic even at its low exposure levels including the human reference dose.     

Fluorescence fingerprints to monitor total trihalomethanes and N-nitrosodimethylamine formation potentials in water

Water samples from 56 lakes of Missouri, USA, were analysed for their fluorescence excitation/emission matrix (EEM) spectroscopy and the formation potentials of total trihalomethanes (TTHM) and N-nitrosodimethylamine (NDMA). Comparing the excitation/emission matrix fingerprints with trihalomethanes formation revealed that water with higher fluorescence intensity generally exhibited higher trihalomethanes formation potential. Moreover, waters with fluorescence centre at excitation: 290–310 nm/emission: 330–350 nm were related to high N-nitrosodimethylamine and trihalomethanes formation potentials. The results suggest that excitation/emission matrix fingerprints could be used as surrogate parameters for monitoring trihalomethanes and N-nitrosodimethylamine formation potentials.