PMID- 35322186 OWN - NLM STAT- MEDLINE DCOM- 20221223 LR - 20230915 IS - 1530-0447 (Electronic) IS - 0031-3998 (Print) IS - 0031-3998 (Linking) VI - 92 IP - 6 DP - 2022 Dec TI - Hematological changes in neonatal mice with phlebotomy-induced anemia. PG - 1575-1579 LID - 10.1038/s41390-022-02023-w [doi] AB - BACKGROUND: Anemia is a nearly universal diagnosis in preterm infants, caused by phlebotomy, and exacerbated by the underlying erythropoietic immaturity. Newborn infants are exposed to the unique stressor of fetal-to-neonatal transition, which requires significant adaptation ex utero. Accordingly, the preterm infant's response to anemia may alter the ability to confront underlying illness. This study utilized our preclinical mouse model of phlebotomy-induced anemia (PIA) to comprehensively investigate associated hematological changes. METHODS: C57BL/6 mice were subjected to timed phlebotomy between postnatal days 2--10 to induce severe anemia. Complete blood counts were determined by the Sysmex XT-2000iV analyzer. RESULTS: Anemic pups showed a gradual reduction of RBC and hemoglobin (Hb) and increased reticulocyte (RET) counts and red cell distribution width (RDW), however, with reduced RET-Hb from postnatal day (P) of 4 onwards. Elevated levels of high fluorescent RET and immature reticulocyte fraction (IRF) were noted in anemic mouse pups, but low and medium fluorescent RET were reduced. Also, the reduction of mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), and mean corpuscular hemoglobin concentration (MCHC) were noted in anemic pups. No changes were seen in lymphocytes, but monocytes and neutrophils were significantly elevated from P4-P6. CONCLUSIONS: PIA in mouse pups is associated with hematological changes that may be exacerbating factors in neonatal diseases. IMPACT: Anemia is common and often severe in premature infants. Investigation of hematological parameters in settings of preclinical anemia may be an index of therapeutic strategies. Preclinical model evaluating the effects of neonatal anemia on the remainder of complete blood count. Detailed time kinetic phlebotomy-induced anemic mice enable us to study the impact on developmental delays in erythropoiesis and possible strategic intervention. Hematological effects of severe anemia in mice might provide insight on how best to investigate anemia in preterm infants. CI - (c) 2022. The Author(s), under exclusive licence to the International Pediatric Research Foundation, Inc. FAU - Chung, Yerin AU - Chung Y AD - Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA. FAU - Desiraju, Suneetha AU - Desiraju S AD - Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA. FAU - Namachivayam, Kopperuncholan AU - Namachivayam K AD - Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA. FAU - Guzman, Pierre AU - Guzman P AD - Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA. FAU - He, Ling AU - He L AD - Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA. AD - Department of Pharmacology & Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA. FAU - MohanKumar, Krishnan AU - MohanKumar K AD - Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA. mohank@jhmi.edu. LA - eng GR - R01 HL133022/HL/NHLBI NIH HHS/United States GR - R01 HL124078/HL/NHLBI NIH HHS/United States GR - R01 HL163043/HL/NHLBI NIH HHS/United States GR - R21 HD105880/HD/NICHD NIH HHS/United States GR - R01 DK120309/DK/NIDDK NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural DEP - 20220323 PL - United States TA - Pediatr Res JT - Pediatric research JID - 0100714 SB - IM MH - Infant, Newborn MH - Humans MH - Animals MH - Mice MH - Animals, Newborn MH - *Phlebotomy/adverse effects MH - Infant, Premature MH - Mice, Inbred C57BL MH - *Anemia/complications PMC - PMC9500113 MID - NIHMS1793401 COIS- COMPETING INTERESTS The authors declare no competing interests. EDAT- 2022/03/25 06:00 MHDA- 2022/12/24 06:00 PMCR- 2022/12/24 CRDT- 2022/03/24 05:38 PHST- 2021/10/06 00:00 [received] PHST- 2022/03/06 00:00 [accepted] PHST- 2021/11/18 00:00 [revised] PHST- 2022/03/25 06:00 [pubmed] PHST- 2022/12/24 06:00 [medline] PHST- 2022/03/24 05:38 [entrez] PHST- 2022/12/24 00:00 [pmc-release] AID - 10.1038/s41390-022-02023-w [pii] AID - 10.1038/s41390-022-02023-w [doi] PST - ppublish SO - Pediatr Res. 2022 Dec;92(6):1575-1579. doi: 10.1038/s41390-022-02023-w. Epub 2022 Mar 23.