Intestinal iron absorption is appropriately modulated to match physiological demand for iron in wild-type and iron-loaded Hamp (hepcidin) knockout rats during acute colitis

• Published in: PloS one 2021-06, Vol.16 (6), p.e0252998-e0252998
• Main Authors: Flores, Shireen R. L, Nelson, Savannah, Woloshun, Regina R, Wang, Xiaoyu, Ha, Jung-Heun, Lee, Jennifer K, Yu, Yang, Merlin, Didier, Collins, James F
• Format: Article
• Language: English
• Subjects: Absorption; Agricultural engineering; Anemia; Animal experimentation; Biology and Life Sciences; Care and treatment; Colitis; Data analysis; Diet; Disease; Editing; Evaluation; Excretory system; Experiments; Food; Food processing; Food quality; Food science; Functional foods & nutraceuticals; Health care facilities; Hepcidin; Homeostasis; Human nutrition; Hypoxia; Inflammation; Inflammatory bowel disease; Iron; Iron in the body; Medicine and Health Sciences; Nutrition; Peptides; Physical Sciences; Physiology; Properties; Research and Analysis Methods; Research facilities; Reviews; Spleen; Ulcerative colitis
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0252998

Mucosal damage, barrier breach, inflammation, and iron-deficiency anemia (IDA) typify ulcerative colitis (UC) in humans. The anemia in UC appears to mainly relate to systemic inflammation. The pathogenesis of this ‘anemia of inflammation’ (AI) involves cytokine-mediated transactivation of hepatic Hamp (encoding the iron-regulatory hormone, hepcidin). In AI, high hepcidin represses iron absorption (and iron release from stores), thus lowering serum iron, and restricting iron for erythropoiesis (causing anemia). In less-severe disease states, inflammation may be limited to the intestine, but whether this perturbs iron homeostasis is uncertain. We hypothesized that localized gut inflammation will increase overall iron demand (to support the immune response and tissue repair), and that hepatic Hamp expression will decrease in response, thus derepressing (i.e., enhancing) iron absorption. Accordingly, we developed a rat model of mild, acute colitis, and studied iron absorption and homeostasis. Rats exposed (orally) to DSS (4%) for 7 days had intestinal (but not systemic) inflammation, and biomarker analyses demonstrated that iron utilization was elevated. Iron absorption was enhanced (by 2-3-fold) in DSS-treated, WT rats of both sexes, but unexpectedly, hepatic Hamp expression was not suppressed. Therefore, to gain a better understanding of regulation of iron absorption during acute colitis, Hamp KO rats were used for further experimentation. The severity of DSS-colitis was similar in Hamp KOs as in WT controls. In the KOs, increased iron requirements associated with the physiological response to colitis were satisfied by mobilizing hepatic storage iron, rather than by increasing absorption of enteral iron (as occurred in WT rats). In conclusion then, in both sexes and genotypes of rats, iron absorption was appropriately modulated to match physiological demand for dietary iron during acute intestinal inflammation, but regulatory mechanisms may not involve hepcidin.