Literature DB >> 9182035

Economical test methods for developmental neurobehavioral toxicity.

G Bignami1.   

Abstract

The assessment of behavioral changes produced by prenatal or early postnatal exposure to potentially noxious agents requires both the designing of ad hoc tests and the adaptation of tests for adult animals to the characteristics of successive developmental stages. The experience in designing tests is still more limited than in the adaptation of tests, but several tests have already proven their usefulness; some examples are the suckling test, the homing test, and evaluations of dam-pup and pup-pup interactions. Functional observational batteries can exploit the development at specified postnatal ages of several reflexes and responses that are absent at birth in altricial rodent species with a short pregnancy such as the rat and the mouse. In neonates, the assessment of early treatment effects can rely not only on deviations from normal responding but also on changes in the time of appearance of otherwise normal response patterns. The same applies to other end points such as responses to pain and various types of spontaneous motor/exploratory activities, including reactivity to a variety of drug challenges that can provide information on the regulatory systems whose development may be affected by early treatments. In particular, the analysis of ontogenetic dissociations (i.e., differential early treatment effects depending jointly on developmental stage at the time of exposure, age of testing, and response end point) can be of considerable value in the study of treatments' mechanisms of action. Overall, it appears that behavioral teratological assessments can be effectively used both proactively, i.e., in risk assessment prior to any human exposure, and reactively. In the latter case, these assessments could have special value in the face of agents suspected to produce borderline changes in developing humans, whose innocuousness or noxiousness can be difficult to establish in the absence of hard evidence of teratogenicity.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 9182035      PMCID: PMC1469583          DOI: 10.1289/ehp.96104s2285

Source DB:  PubMed          Journal:  Environ Health Perspect        ISSN: 0091-6765            Impact factor:   9.031


  85 in total

1.  The health effects of low level exposure to lead.

Authors:  H L Needleman; D Bellinger
Journal:  Annu Rev Public Health       Date:  1991       Impact factor: 21.981

2.  Postnatal behavioral effects in mice after prenatal exposure to methylmercury.

Authors:  J A Hughes; Z Annau
Journal:  Pharmacol Biochem Behav       Date:  1976-04       Impact factor: 3.533

3.  Medium and long-term behavioral effects in mice of extended gestational exposure to ozone.

Authors:  S Petruzzi; M Fiore; G Dell'Omo; G Bignami; E Alleva
Journal:  Neurotoxicol Teratol       Date:  1995 Jul-Aug       Impact factor: 3.763

4.  Collaborative Behavioral Teratology Study: protocol design and testing procedures.

Authors:  J Adams; J Buelke-Sam; C A Kimmel; C J Nelson; L W Reiter; T J Sobotka; H A Tilson; B K Nelson
Journal:  Neurobehav Toxicol Teratol       Date:  1985 Nov-Dec

5.  Behavioural effects of selective mu-, kappa-, and delta-opioid agonists in neonatal rats.

Authors:  H C Jackson; I Kitchen
Journal:  Psychopharmacology (Berl)       Date:  1989       Impact factor: 4.530

6.  Fractional escape and avoidance on a titration schedule.

Authors:  B WEISS; V G LATIES
Journal:  Science       Date:  1958-12-19       Impact factor: 47.728

7.  Sexual segregation in infancy and bi-directional benzodiazepine effects on hot-plate response and neophobia in adult mice.

Authors:  G Laviola; G Loggi
Journal:  Pharmacol Biochem Behav       Date:  1992-08       Impact factor: 3.533

8.  Prenatal methyl mercury exposure: I. Alterations in neonatal activity.

Authors:  C U Eccles; Z Annau
Journal:  Neurobehav Toxicol Teratol       Date:  1982 May-Jun

9.  Dose-response effects of prenatal phenytoin exposure in rats: effects on early locomotion, maze learning, and memory as a function of phenytoin-induced circling behavior.

Authors:  W P Weisenburger; D R Minck; K D Acuff; C V Vorhees
Journal:  Neurotoxicol Teratol       Date:  1990 Mar-Apr       Impact factor: 3.763

10.  Hyperresponsiveness to methylphenidate in rats following prenatal ethanol exposure.

Authors:  L W Means; C W Medlin; V D Hughes; S L Gray
Journal:  Neurobehav Toxicol Teratol       Date:  1984 May-Jun
View more
  13 in total

1.  Neurobehavioral Alterations in a Genetic Murine Model of Feingold Syndrome 2.

Authors:  E Fiori; L Babicola; D Andolina; A Coassin; T Pascucci; L Patella; Y-C Han; A Ventura; R Ventura
Journal:  Behav Genet       Date:  2015-05-31       Impact factor: 2.805

2.  Synthetic Thymidine Analog Labeling without Misconceptions.

Authors:  Anna Ivanova; Olesya Gruzova; Elizaveta Ermolaeva; Olga Astakhova; Sheed Itaman; Grigori Enikolopov; Alexander Lazutkin
Journal:  Cells       Date:  2022-06-10       Impact factor: 7.666

Review 3.  Appropriate end points for the characterization of behavioral changes in developmental toxicology.

Authors:  V Cuomo; M A De Salvia; S Petruzzi; E Alleva
Journal:  Environ Health Perspect       Date:  1996-04       Impact factor: 9.031

Review 4.  Animal behavioral methods in neurotoxicity assessment: SGOMSEC joint report.

Authors:  B Kulig; E Alleva; G Bignami; J Cohn; D Cory-Slechta; V Landa; J O'Donoghue; D Peakall
Journal:  Environ Health Perspect       Date:  1996-04       Impact factor: 9.031

5.  Sex-specific behavioural deficits induced at early life by prenatal exposure to the cannabinoid receptor agonist WIN55, 212-2 depend on mGlu5 receptor signalling.

Authors:  Antonia Manduca; Michela Servadio; Francesca Melancia; Sara Schiavi; Olivier J Manzoni; Viviana Trezza
Journal:  Br J Pharmacol       Date:  2020-01-03       Impact factor: 8.739

6.  Cannabinoid Exposure via Lactation in Rats Disrupts Perinatal Programming of the Gamma-Aminobutyric Acid Trajectory and Select Early-Life Behaviors.

Authors:  Andrew F Scheyer; Milene Borsoi; Jim Wager-Miller; Anne-Laure Pelissier-Alicot; Michelle N Murphy; Ken Mackie; Olivier J J Manzoni
Journal:  Biol Psychiatry       Date:  2019-09-05       Impact factor: 13.382

7.  Long-term effects of environmentally relevant doses of 2,2',4,4',5,5' hexachlorobiphenyl (PCB153) on neurobehavioural development, health and spontaneous behaviour in maternally exposed mice.

Authors:  Marte Haave; Annette Bernhard; Finn K Jellestad; Einar Heegaard; Trond Brattelid; Anne-Katrine Lundebye
Journal:  Behav Brain Funct       Date:  2011-01-13       Impact factor: 3.759

8.  Cerebral gene expression and neurobehavioural development after perinatal exposure to an environmentally relevant polybrominated diphenylether (BDE47).

Authors:  Marte Haave; Kristin Ingvaldsen Folven; Thomas Carroll; Chris Glover; Einar Heegaard; Trond Brattelid; Christer Hogstrand; Anne-Katrine Lundebye
Journal:  Cell Biol Toxicol       Date:  2011-06-02       Impact factor: 6.691

Review 9.  Methods to identify and characterize developmental neurotoxicity for human health risk assessment. III: pharmacokinetic and pharmacodynamic considerations.

Authors:  D C Dorman; S L Allen; J Z Byczkowski; L Claudio; J E Fisher; J W Fisher; G J Harry; A A Li; S L Makris; S Padilla; L G Sultatos; B E Mileson
Journal:  Environ Health Perspect       Date:  2001-03       Impact factor: 9.031

10.  Prenatal chlorpyrifos exposure alters motor behavior and ultrasonic vocalization in CD-1 mouse pups.

Authors:  Aldina Venerosi; Laura Ricceri; Maria Luisa Scattoni; Gemma Calamandrei
Journal:  Environ Health       Date:  2009-03-30       Impact factor: 5.984

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.