Literature DB >> 27094606

A novel, ecologically relevant, highly preferred, and non-invasive means of oral substance administration for rodents.

Marissa Sobolewski1, Joshua L Allen2, Keith Morris-Schaffer3, Carolyn Klocke4, Katherine Conrad5, Deborah A Cory-Slechta6.   

Abstract

Prenatal stress and nutrition are well-known to alter a broad range of physiological systems, notably metabolic, endocrine and neurobehavioral function. Commonly used methods for oral administration of xenobiotics can, by acting as a stressor or altering normal nutrition intake, alter these physiological systems as well. Taken together, oral administration methods may unintentionally introduce confounding physiological effects that can mask or enhance toxicity of xenobiotics, particularly if they share biological targets. Consequently, it should be preferable to develop alternative methods without these potential confounds. The aim of this study was to determine the suitability of mealworms as an alternative treat-based method to deliver xenobiotics via the orogastric route. Accurate oral administration is contingent on motivation and preference; mice reliably preferred mealworms over wafer cookie treats. Further, ingestion of wafer cookies significantly increased mouse blood glucose levels, whereas unaltered mealworms produced no such change. Mealworms functioned effectively to orally administer glucose, as glucose-spiked mealworms produced a rise in blood glucose equivalent to the ingestion of the wafer cookie. Mealworms did not interfere with the physiological function of orally administered d-amphetamine, as both mealworm and oral gavage administered d-amphetamine showed similar alterations in locomotor behavior (mice did not fully consume d-amphetamine-dosed cookies and thus could not be compared). Collectively, the findings indicate that mealworms are a preferred and readily consumed treat, which importantly mimics environmental-relevant nutritional intake, and mealworms per se do not alter glucose metabolic pathways. Additionally, mealworms accurately delivered xenobiotics into blood circulation and did not interfere with the physiological function of administered xenobiotics. Thus mealworm-based oral administration may be a preferable and accurate route of xenobiotic administration that eliminates physiological alterations associated with other methods of delivery.
Copyright © 2016. Published by Elsevier Inc.

Entities:  

Keywords:  Experimental confounds; Mealworm; Nutrition; Oral administration; Rodent; Stress

Mesh:

Substances:

Year:  2016        PMID: 27094606      PMCID: PMC5663185          DOI: 10.1016/j.ntt.2016.04.002

Source DB:  PubMed          Journal:  Neurotoxicol Teratol        ISSN: 0892-0362            Impact factor:   3.763


  31 in total

1.  Alternative method of oral dosing for rats.

Authors:  Zeenat Atcha; Claire Rourke; Aveline Hp Neo; Catherine Wh Goh; Jean Sk Lim; Chiu-Cheong Aw; Edward R Browne; Darrel J Pemberton
Journal:  J Am Assoc Lab Anim Sci       Date:  2010-05       Impact factor: 1.232

2.  Voluntary ingestion of antiparasitic drugs emulsified in honey represents an alternative to gavage in mice.

Authors:  Tatiana Küster; Beatrice Zumkehr; Corina Hermann; Regula Theurillat; Wolfgang Thormann; Bruno Gottstein; Andrew Hemphill
Journal:  J Am Assoc Lab Anim Sci       Date:  2012-03       Impact factor: 1.232

Review 3.  Maternal and early life stress effects on immune function: relevance to immunotoxicology.

Authors:  Denise L Bellinger; Cheri Lubahn; Dianne Lorton
Journal:  J Immunotoxicol       Date:  2008-10       Impact factor: 3.000

4.  Epigenetic transgenerational inheritance of altered stress responses.

Authors:  David Crews; Ross Gillette; Samuel V Scarpino; Mohan Manikkam; Marina I Savenkova; Michael K Skinner
Journal:  Proc Natl Acad Sci U S A       Date:  2012-05-21       Impact factor: 11.205

Review 5.  Epigenetic and transgenerational reprogramming of brain development.

Authors:  Tracy L Bale
Journal:  Nat Rev Neurosci       Date:  2015-04-29       Impact factor: 34.870

6.  Enhanced learning deficits in female rats following lifetime pb exposure combined with prenatal stress.

Authors:  Deborah A Cory-Slechta; Sander Stern; Doug Weston; Joshua L Allen; Sue Liu
Journal:  Toxicol Sci       Date:  2010-07-16       Impact factor: 4.849

7.  Noninvasive corticosterone treatment rapidly increases activity in Gambel's white-crowned sparrows (Zonotrichia leucophrys gambelii).

Authors:  C W Breuner; A L Greenberg; J C Wingfield
Journal:  Gen Comp Endocrinol       Date:  1998-09       Impact factor: 2.822

8.  Polychlorinated biphenyls (Aroclor 1254) do not uniformly produce agonist actions on thyroid hormone responses in the developing rat brain.

Authors:  Ruby Bansal; R Thomas Zoeller
Journal:  Endocrinology       Date:  2008-04-17       Impact factor: 4.736

9.  Dosing-induced stress causes hepatocyte apoptosis in rats primed by the rodent nongenotoxic hepatocarcinogen cyproterone acetate.

Authors:  R A Roberts; A R Soames; N H James; J H Gill; E B Wheeldon
Journal:  Toxicol Appl Pharmacol       Date:  1995-12       Impact factor: 4.219

10.  Prenatal stress, glucocorticoids and the programming of adult disease.

Authors:  Elizabeth C Cottrell; Jonathan R Seckl
Journal:  Front Behav Neurosci       Date:  2009-09-07       Impact factor: 3.558

View more
  3 in total

1.  Selective memory and behavioral alterations after ambient ultrafine particulate matter exposure in aged 3xTgAD Alzheimer's disease mice.

Authors:  Katrina Jew; Denise Herr; Candace Wong; Andrea Kennell; Keith Morris-Schaffer; Günter Oberdörster; M Kerry O'Banion; Deborah A Cory-Slechta; Alison Elder
Journal:  Part Fibre Toxicol       Date:  2019-11-26       Impact factor: 9.400

2.  Effects of gestational low dose perfluorooctanoic acid on maternal and "anxiety-like" behavior in dams.

Authors:  Alyssa K Merrill; Katherine Conrad; Elena Marvin; Marissa Sobolewski
Journal:  Front Toxicol       Date:  2022-08-29

3.  Protracted Impairment of Maternal Metabolic Health in Mouse Dams Following Pregnancy Exposure to a Mixture of Low Dose Endocrine-Disrupting Chemicals, a Pilot Study.

Authors:  Alyssa K Merrill; Timothy Anderson; Katherine Conrad; Elena Marvin; Tamarra James-Todd; Deborah A Cory-Slechta; Marissa Sobolewski
Journal:  Toxics       Date:  2021-12-09
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.