and are intravascular, parasitic flatworms that infect >250 million people in 70 developing countries, yet not all people of the same community and household are afflicted. Regarding laboratory rodents, mice but not rats are susceptible to infection with and hamsters but not mice are entirely permissive to infection with . A recent Brazilian publication has demonstrated that resistance of the water-rat, to infection might be ascribed to stores of arachidonic acid (ARA)-rich lipids in liver. Several reports have previously shown that ARA is a safe and effective schistosomicide , and in mice, hamsters and in children appeared more sensitive than to ARA in and experiments. Accordingly, it was proposed that ARA increased levels might be predominantly responsible for natural attrition of and in resistant experimental rodents. Therefore, the levels of ARA in serum, lung, and liver of rats (resistant) and mice (susceptible) at 1, 2, 3, 4 and 6 weeks after infection with cercariae and between mice (semi-permissive) and hamster (susceptible) at 1, 2, 3, 4, and 12 weeks after infection with . cercariae were compared and contrasted. Neutral triglycerides and ARA levels were assessed in serum using commercially available assays and in liver and lung sections by transmission electron microscopy, Oil Red O staining, and specific anti-ARA antibody-based immunohistochemistry assays. Significant ( < .05), consistent, and reproducible correlation was recorded between ARA content in serum, lung, and liver and rodent resistance to schistosome infection, thereby implicating ARA as an endoschistosomicide.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052652 | PMC |
http://dx.doi.org/10.1016/j.jare.2018.01.005 | DOI Listing |
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