Literature DB >> 27175970

To Cull or Not To Cull? Considerations for Studies of Endocrine-Disrupting Chemicals.

Alexander Suvorov1, Laura N Vandenberg1.   

Abstract

The power of animal models is derived from the ability to control experimental variables so that observed effects may be unequivocally attributed to the factor that was changed. One variable that is difficult to control in animal experiments is the number and composition of offspring in a litter. To account for this variability, artificial equalization of the number of offspring in a litter (culling) is often used. The rationale for culling, however, has always been controversial. The Developmental Origins of Health and Disease concept provides a new context to evaluate the pros and cons of culling in laboratory animal studies, especially in the context of endocrine-disrupting chemicals. Emerging evidence indicates that culling, especially of large litters, can drastically change the feeding status of a pup, which can result in compensatory growth with long-term consequences for the animal, including increased risk of cardio-metabolic diseases. Similarly, culling of litters to intentionally bias sex ratios can alter the animal's behavior and physiology, with effects observed on a wide range of outcomes. Thus, in an attempt to control for variability in developmental rates, culling introduces an uncontrolled or confounding variable, which itself may affect a broad spectrum of health-related consequences. Variabilities in culling protocols could be responsible for differences in responses to endocrine-disrupting chemicals reported across studies. Because litter sex composition and size are vectors that can influence both prenatal and postnatal growth, they are essential considerations for the interpretation of results from laboratory animal studies.

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Year:  2016        PMID: 27175970      PMCID: PMC4929555          DOI: 10.1210/en.2016-1145

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  54 in total

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Authors:  Laura N Vandenberg; Theo Colborn; Tyrone B Hayes; Jerrold J Heindel; David R Jacobs; Duk-Hee Lee; Toshi Shioda; Ana M Soto; Frederick S vom Saal; Wade V Welshons; R Thomas Zoeller; John Peterson Myers
Journal:  Endocr Rev       Date:  2012-03-14       Impact factor: 19.871

2.  Intake and use of milk nutrients by rat pups suckled in small, medium, or large litters.

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3.  Effect of size and sex ration of litter on the sexual maturation of female mice.

Authors:  L C Drickamer
Journal:  J Reprod Fertil       Date:  1976-03

4.  Redistribution of glucose from skeletal muscle to adipose tissue during catch-up fat: a link between catch-up growth and later metabolic syndrome.

Authors:  Philippe Cettour-Rose; Sonia Samec; Aaron P Russell; Serge Summermatter; Davide Mainieri; Claudia Carrillo-Theander; Jean-Pierre Montani; Josiane Seydoux; Françoise Rohner-Jeanrenaud; Abdul G Dulloo
Journal:  Diabetes       Date:  2005-03       Impact factor: 9.461

Review 5.  A new approach to synergize academic and guideline-compliant research: the CLARITY-BPA research program.

Authors:  Thaddeus T Schug; Jerrold J Heindel; Luísa Camacho; K Barry Delclos; Paul Howard; Anne F Johnson; Jason Aungst; Dennis Keefe; Retha Newbold; Nigel J Walker; R Thomas Zoeller; John R Bucher
Journal:  Reprod Toxicol       Date:  2013-06-05       Impact factor: 3.143

6.  Perinatal elevation of hypothalamic insulin, acquired malformation of hypothalamic galaninergic neurons, and syndrome x-like alterations in adulthood of neonatally overfed rats.

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Journal:  Brain Res       Date:  1999-07-31       Impact factor: 3.252

7.  Effect of litter size on milk yield in the rat.

Authors:  M Morag; F Popliker; R Yagil
Journal:  Lab Anim       Date:  1975-01       Impact factor: 2.471

Review 8.  Pathways from weight fluctuations to metabolic diseases: focus on maladaptive thermogenesis during catch-up fat.

Authors:  A G Dulloo; J Jacquet; J-P Montani
Journal:  Int J Obes Relat Metab Disord       Date:  2002-09

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10.  Parma consensus statement on metabolic disruptors.

Authors:  Jerrold J Heindel; Frederick S Vom Saal; Bruce Blumberg; Patrizia Bovolin; Gemma Calamandrei; Graziano Ceresini; Barbara A Cohn; Elena Fabbri; Laura Gioiosa; Christopher Kassotis; Juliette Legler; Michele La Merrill; Laura Rizzir; Ronit Machtinger; Alberto Mantovani; Michelle A Mendez; Luisa Montanini; Laura Molteni; Susan C Nagel; Stefano Parmigiani; Giancarlo Panzica; Silvia Paterlini; Valentina Pomatto; Jérôme Ruzzin; Giorgio Sartor; Thaddeus T Schug; Maria E Street; Alexander Suvorov; Riccardo Volpi; R Thomas Zoeller; Paola Palanza
Journal:  Environ Health       Date:  2015-06-20       Impact factor: 5.984

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  14 in total

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Journal:  Neurotoxicol Teratol       Date:  2016-09-12       Impact factor: 3.763

2.  Prenatal Exposure to Unconventional Oil and Gas Operation Chemical Mixtures Altered Mammary Gland Development in Adult Female Mice.

Authors:  Sarah A Sapouckey; Christopher D Kassotis; Susan C Nagel; Laura N Vandenberg
Journal:  Endocrinology       Date:  2018-03-01       Impact factor: 4.736

3.  Bisphenol S (BPS) Alters Maternal Behavior and Brain in Mice Exposed During Pregnancy/Lactation and Their Daughters.

Authors:  Mary C Catanese; Laura N Vandenberg
Journal:  Endocrinology       Date:  2017-03-01       Impact factor: 4.736

4.  Adverse Reproductive and Developmental Health Outcomes Following Prenatal Exposure to a Hydraulic Fracturing Chemical Mixture in Female C57Bl/6 Mice.

Authors:  Christopher D Kassotis; John J Bromfield; Kara C Klemp; Chun-Xia Meng; Andrew Wolfe; R Thomas Zoeller; Victoria D Balise; Chiamaka J Isiguzo; Donald E Tillitt; Susan C Nagel
Journal:  Endocrinology       Date:  2016-08-25       Impact factor: 4.736

5.  Developmental Exposure to 2,2',4,4'-Tetrabromodiphenyl Ether Induces Long-Lasting Changes in Liver Metabolism in Male Mice.

Authors:  Ahmed Khalil; Mikhail Parker; Richard Mpanga; Sebnem E Cevik; Cassandra Thorburn; Alexander Suvorov
Journal:  J Endocr Soc       Date:  2017-03-14

6.  Transcriptomic Analysis of Gonadal Adipose Tissue in Male Mice Exposed Perinatally to 2,2',4,4'-Tetrabromodiphenyl Ether (BDE-47).

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7.  Effects of Perinatal Exposure to Dibutyltin Chloride on Fat and Glucose Metabolism in Mice, and Molecular Mechanisms, in Vitro.

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8.  Dose threshold for radiation induced fetal programming in a mouse model at 4 months of age: Hepatic expression of genes and proteins involved in glucose metabolism and glucose uptake in brown adipose tissue.

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Journal:  PLoS One       Date:  2020-04-21       Impact factor: 3.240

9.  Developmental 2,3,7,8-tetrachlorodibenzo-p-dioxin exposure of either parent enhances the risk of necrotizing enterocolitis in neonatal mice.

Authors:  Shilpa Mokshagundam; Tianbing Ding; Jelonia T Rumph; Madison Dallas; Victoria R Stephens; Kevin G Osteen; Kaylon L Bruner-Tran
Journal:  Birth Defects Res       Date:  2020-06-09       Impact factor: 2.661

10.  Developmental Exposure to 2,2',4,4'-Tetrabromodiphenyl Ether Permanently Alters Blood-Liver Balance of Lipids in Male Mice.

Authors:  Ahmed Khalil; Sebnem E Cevik; Stephanie Hung; Sridurgadevi Kolla; Monika A Roy; Alexander Suvorov
Journal:  Front Endocrinol (Lausanne)       Date:  2018-09-20       Impact factor: 5.555

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