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Haemolysis Overestimates Plasma Oxidative Stress Biomarkers in a Free-Ranging Mammal

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/bies.201300108openalex-snapshot

Oxidative stress as a cost of reproduction: Beyond the simplistic trade‐off model

inferredcites →https://doi.org/10.1002/ece3.1771openalex-snapshot

Plasma markers of oxidative stress are uncorrelated in a wild mammal

inferredcites →https://doi.org/10.1002/ece3.1790openalex-snapshot

Oxidative stress and life histories: unresolved issues and current needs

inferredcites →https://doi.org/10.1002/ece3.2080openalex-snapshot

Meta‐analysis indicates that oxidative stress is both a constraint on and a cost of growth

inferredcites →https://doi.org/10.1002/ece3.4187openalex-snapshot

Oxidative damage and antioxidant defense are assay and tissue‐dependent both in captive and wild‐caught bank voles (Myodes glareolus) before and after reproduction

inferredcites →https://doi.org/10.1002/ece3.786openalex-snapshot

Manipulating reproductive effort leads to changes in female reproductive scheduling but not oxidative stress

inferredcites →https://doi.org/10.1007/s10695-017-0359-yopenalex-snapshot

Hemolysis interference in measuring fish plasma biochemical indicators

inferredcites →https://doi.org/10.1016/0076-6879(90)86141-hopenalex-snapshot

[49] Determination of carbonyl content in oxidatively modified proteins

inferredcites →https://doi.org/10.1016/0378-4347(92)80593-fopenalex-snapshot

High-performance liquid chromatographic separation of malondialdehyde—thiobarbituric acid adduct in biological materials (plasma and human cells) using a commercially available reagent

inferredcites →https://doi.org/10.1016/j.ab.2016.10.021openalex-snapshot

Assessment of lipid peroxidation by measuring malondialdehyde (MDA) and relatives in biological samples: Analytical and biological challenges

inferredcites →https://doi.org/10.1016/j.cbpb.2006.12.015openalex-snapshot

Measuring circulating antioxidants in wild birds

inferredcites →https://doi.org/10.1016/j.clinbiochem.2009.10.002openalex-snapshot

Human plasma concentrations of malondialdehyde (MDA) and the F2-isoprostane 15(S)-8-iso-PGF2α may be markedly compromised by hemolysis: Evidence by GC-MS/MS and potential analytical and biological ramifications

inferredcites →https://doi.org/10.1016/j.clinbiochem.2012.08.002openalex-snapshot

Effectiveness of practices to reduce blood sample hemolysis in EDs: A laboratory medicine best practices systematic review and meta-analysis

inferredcites →https://doi.org/10.1016/j.clinbiochem.2017.09.013openalex-snapshot

Causes, consequences and management of sample hemolysis in the clinical laboratory

inferredcites →https://doi.org/10.1016/j.mad.2007.06.007openalex-snapshot

Influence of age on the stability of human erythrocyte membranes

inferredcites →https://doi.org/10.1016/j.tree.2012.06.006openalex-snapshot

Oxidative damage, ageing, and life-history evolution: where now?

inferredcites →https://doi.org/10.1016/j.tree.2013.01.015openalex-snapshot

Does reproduction cause oxidative stress? An open question

inferredcites →https://doi.org/10.1016/s0009-8981(03)00003-2openalex-snapshot

Protein carbonyl groups as biomarkers of oxidative stress

inferredcites →https://doi.org/10.1016/s0034-5288(18)30951-2openalex-snapshot

Effect of physical restraint and xylazine sedation on haematological values in red deer (Cervus elaphus)

inferredcites →https://doi.org/10.1016/s0531-5565(03)00159-1openalex-snapshot

Growth versus lifespan: perspectives from evolutionary ecology

inferredcites →https://doi.org/10.1016/s0921-4488(01)00266-8openalex-snapshot

Effects of sample handling, processing, storage, and hemolysis on measurements of key energy metabolites in ovine blood

inferredcites →https://doi.org/10.1016/s1357-2725(99)00034-5openalex-snapshot

Quantitation of oxidative damage to tissue proteins

inferredcites →https://doi.org/10.1016/s1537-1891(02)00298-7openalex-snapshot

Blood sample stability at room temperature for counting red and white blood cells and platelets

inferredcites →https://doi.org/10.1038/35041687openalex-snapshot

Oxidants, oxidative stress and the biology of ageing

inferredcites →https://doi.org/10.1038/s41559-022-01940-7openalex-snapshot

The expanding value of long-term studies of individuals in the wild

inferredcites →https://doi.org/10.1038/s42255-022-00591-zopenalex-snapshot

Guidelines for measuring reactive oxygen species and oxidative damage in cells and in vivo

inferredcites →https://doi.org/10.1053/rvsc.1998.0248openalex-snapshot

Effect of the method of capture on the haematology and blood chemistry of red deer (Cervus elaphus)

inferredcites →https://doi.org/10.1053/tmrv.2002.29404openalex-snapshot

Red blood cell hemolysis during processing

inferredcites →https://doi.org/10.1093/acprof:oso/9780198717478.001.0001openalex-snapshot

Free Radicals in Biology and Medicine

inferredcites →https://doi.org/10.1093/biosci/biw176openalex-snapshot

The Oxidative Cost of Reproduction: Theoretical Questions and Alternative Mechanisms

inferredcites →https://doi.org/10.1093/clinchem/46.2.306openalex-snapshot

Hemolyzed Specimens: A Reason for Rejection or a Clinical Challenge?

inferredcites →https://doi.org/10.1093/conphys/coac018openalex-snapshot

A meta-analysis of impacts of immune response and infection on oxidative status in vertebrates

inferredcites →https://doi.org/10.1098/rsbl.2004.0171openalex-snapshot

Birds sacrifice oxidative protection for reproduction

inferredcites →https://doi.org/10.1098/rspb.2008.1791openalex-snapshot

Reactive oxygen species as universal constraints in life-history evolution

inferredcites →https://doi.org/10.1111/brv.12179openalex-snapshot

Oxidative shielding and the cost of reproduction

inferredcites →https://doi.org/10.1111/brv.13012openalex-snapshot

Defence against the intergenerational cost of reproduction in males: oxidative shielding of the germline

inferredcites →https://doi.org/10.1111/j.0030-1299.2006.14447.xopenalex-snapshot

Using a proxy of plant productivity (NDVI) to find key periods for animal performance: the case of roe deer

inferredcites →https://doi.org/10.1111/j.1365-2435.2009.01555.xopenalex-snapshot

Life history correlates of oxidative damage in a free‐living mammal population

inferredcites →https://doi.org/10.1111/j.1365-2435.2010.01750.xopenalex-snapshot

Oxidative stress as a life‐history constraint: the role of reactive oxygen species in shaping phenotypes from conception to death

inferredcites →https://doi.org/10.1111/j.1365-2435.2010.01755.xopenalex-snapshot

How to measure oxidative stress in an ecological context: methodological and statistical issues

inferredcites →https://doi.org/10.1111/j.1365-2435.2010.01772.xopenalex-snapshot

The ecological significance of antioxidants and oxidative stress: a marriage between mechanistic and functional perspectives

inferredcites →https://doi.org/10.1111/j.1365-2435.2011.01952.xopenalex-snapshot

Tissue‐dependent changes in oxidative damage with male reproductive effort in house mice

inferredcites →https://doi.org/10.1111/j.1461-0248.2004.00594.xopenalex-snapshot

Increased susceptibility to oxidative stress as a proximate cost of reproduction

inferredcites →https://doi.org/10.1111/j.1461-0248.2008.01246.xopenalex-snapshot

Oxidative stress in ecology and evolution: lessons from avian studies

inferredcites →https://doi.org/10.1111/j.1461-0248.2008.01258.xopenalex-snapshot

Oxidative stress as a mediator of life history trade‐offs: mechanisms, measurements and interpretation

inferredcites →https://doi.org/10.1111/j.1937-2817.2010.tb01236.xopenalex-snapshot

Uninformative Parameters and Model Selection Using Akaike's Information Criterion

inferredcites →https://doi.org/10.1111/j.1939-165x.1983.tb00829.xopenalex-snapshot

Effect of in vitro Hemolysis on Values for Certain Porcine Serum Constituents

inferredcites →https://doi.org/10.1111/j.2041-210x.2010.00080.xopenalex-snapshot

On the measurement of circulating antioxidant capacity and the nightmare of uric acid

inferredcites →https://doi.org/10.1111/oik.04421openalex-snapshot

The cost of growing large: costs of post‐weaning growth on body mass senescence in a wild mammal

inferredcites →https://doi.org/10.1111/trf.16264openalex-snapshot

How red blood cell quality is starting to carry its weight

inferredcites →https://doi.org/10.1139/z03-152openalex-snapshot

Body condition in Svalbard reindeer and the use of blood parameters as indicators of condition and fitness

inferredcites →https://doi.org/10.1146/annurev.ecolsys.32.081501.114006openalex-snapshot

The Physiology of Life History Trade-Offs in Animals

inferredcites →https://doi.org/10.1152/japplphysiol.01392.2004openalex-snapshot

Exercise-induced oxidative stress leads hemolysis in sedentary but not trained humans

inferredcites →https://doi.org/10.1155/2011/473709openalex-snapshot

Heme Oxygenase-1: A Critical Link between Iron Metabolism, Erythropoiesis, and Development

inferredcites →https://doi.org/10.11613/bm.2011.040openalex-snapshot

Studies on in vitro hemolysis and utility of corrective formulas for reporting results on hemolyzed specimens

inferredcites →https://doi.org/10.1177/0885066617708992openalex-snapshot

High Hemoglobin Is an Independent Risk Factor for the Development of Hemolysis During Pediatric Extracorporeal Life Support

inferredcites →https://doi.org/10.1242/jeb.114116openalex-snapshot

Does reproduction protect against oxidative stress?

inferredcites →https://doi.org/10.1242/jeb.126557openalex-snapshot

Reproduction is not costly in terms of oxidative stress

inferredcites →https://doi.org/10.1515/cclm-2016-0698openalex-snapshot

The prevalence of hemolysis – a survey using hemolysis index

inferredcites →https://doi.org/10.1515/cclm.2008.170openalex-snapshot

Haemolysis: an overview of the leading cause of unsuitable specimens in clinical laboratories

inferredcites →https://doi.org/10.18637/jss.v067.i01openalex-snapshot

Fitting Linear Mixed-Effects Models Using lme4

inferredcites →https://doi.org/10.2307/3802723openalex-snapshot

Model Selection and Multimodel Inference: A Practical Information-Theoretic Approach

inferredcites →https://doi.org/10.2307/5396openalex-snapshot

Roe Deer Survival Patterns: A Comparative Analysis of Contrasting Populations

inferredcites →https://doi.org/10.2527/jas.53968openalex-snapshot

Blood sampling and hemolysis affect concentration of plasma metabolites1

inferredcites →https://doi.org/10.3109/10408363.2011.600228openalex-snapshot

Hemolyzed specimens: a major challenge for emergency departments and clinical laboratories

inferredcites →https://doi.org/10.3109/10715762.2012.686037openalex-snapshot

The effect of hemolysis on plasma oxidation and nitration in patients with sickle cell disease

inferredcites →https://doi.org/10.3161/000164508x345347openalex-snapshot

Repeatability and Method-Dependent Variation of Blood Parameters in Wild-Caught Great TitsParus major

inferredcites →https://doi.org/10.3389/fphys.2014.00500openalex-snapshot

The pathophysiology of extracellular hemoglobin associated with enhanced oxidative reactions

inferredcites →https://doi.org/10.3390/antiox10060864openalex-snapshot

Blood Plasma Quality Control by Plasma Glutathione Status

inferredcites →https://doi.org/10.3390/diagnostics10010051openalex-snapshot

The Influence of Serum Sample Storage Conditions on Selected Laboratory Parameters Related to Oxidative Stress: A Preliminary Study

inferredcites →https://doi.org/10.7589/0090-3558-39.2.375openalex-snapshot

EFFECTS OF ACEPROMAZINE ON CAPTURE STRESS IN ROE DEER (CAPREOLUS CAPREOLUS)

inferredcites →https://doi.org/10.7589/0090-3558-45.1.73openalex-snapshot

EFFECT OF HEMOLYSIS ON PLASMA PROTEIN LEVELS AND PLASMA ELECTROPHORESIS IN BIRDS

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.70675/cc3b068ez5bdcz4948z8552z09a64e0863d6openalex-snapshot

Restauration de l’agrosystème de la plaine alsacienne à travers la protection d’une espèce emblématique ; le hamster commun

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