System Maintenance Notice

Please note that maintenance work is scheduled between 4 AM and 5 AM - CET. During this time, you may experience reduced performance. Thanks for your patience.

Publications

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural Epublish 3 citations

PubMed: 38706961 DOI: 10.1093/function/zqae009

Hypertension Increases Susceptibility to Experimental Malaria in Mice.

Function (Oxf) 5(3):zqae009

Authors: Mrunmayee R Kandalgaonkar, Beng San Yeoh, Bina Joe, Nathan W Schmidt, Matam Vijay-Kumar, Piu Saha

Affiliations

  • Center for Hypertension and Precision Medicine, Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, OH 43614, USA.
  • Ryan White Center for Pediatric Infectious Diseases and Global Health, Herman B. Wells Center for Pediatric Research, and Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN 46202, USA.

Abstract

Global prevalence of hypertension is on the rise, burdening healthcare, especially in developing countries where infectious diseases, such as malaria, are also rampant. Whether hypertension could predispose or increase susceptibility to malaria, however, has not been extensively explored. Previously, we reported that hypertension is associated with abnormal red blood cell (RBC) physiology and anemia. Since RBC are target host cells for malarial parasite, , we hypothesized that hypertensive patients with abnormal RBC physiology are at greater risk or susceptibility to infection. To test this hypothesis, normotensive (BPN/3J) and hypertensive (BPH/2J) mice were characterized for their RBC physiology and subsequently infected with (), a murine-specific non-lethal strain. When compared to BPN mice, BPH mice displayed microcytic anemia with RBC highly resistant to osmotic hemolysis. Further, BPH RBC exhibited greater membrane rigidity and an altered lipid composition, as evidenced by higher levels of phospholipids and saturated fatty acid, such as stearate (C18:0), along with lower levels of polyunsaturated fatty acid like arachidonate (C20:4). Moreover, BPH mice had significantly greater circulating Ter119 CD71 reticulocytes, or immature RBC, prone to infection. Upon infection with , BPH mice experienced significant body weight loss accompanied by sustained parasitemia, indices of anemia, and substantial increase in systemic pro-inflammatory mediators, compared to BPN mice, indicating that BPH mice were incompetent to clear infection. Collectively, these data demonstrate that aberrant RBC physiology observed in hypertensive BPH mice contributes to an increased susceptibility to infection and malaria-associated pathology.

MeSH

Cells, Malaria, Hypertension, Physiology, Erythrocytes, Reticulocytes, Anemia, Blood Pressure, Physiological Phenomena, Parasites, Infections, Fatty Acids

Cited by