Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText.
Kick-your-searchterm to multiple Engines kick-your-query now !>
A dictionary by aggregated review articles of nephrology, medicine and the life sciences
Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.
garesp_yesshow ga

http://scihub22266oqcxt.onion/10.1016/s0006-8993(02)02724-5
suck pdf from google scholar
PDF vom PMID12106671  :  Publisher
pmid12106671
Nephropedia Template TP

gab.com Text

Twit Text FOAVip

Twit Text #

English Wikipedia


  • Effects of genetic background on neonatal Borna disease virus infection-induced neurodevelopmental damage II Neurochemical alterations and responses to pharmacological treatments #MMPMID12106671
  • Pletnikov MV; Rubin SA; Vogel MW; Moran TH; Carbone KM
  • Brain Res 2002[Jul]; 944 (1-2): 108-23 PMID12106671garesp_yesshow ga
  • The gene-environment interplay is thought to determine variability in clinical conditions and responses to therapy in human neurodevelopmental disorders. Studying abnormal brain and behavior development in inbred strains of rodents can help in the identification of the complex pathogenic mechanisms of the host-environment interaction. This paper is the second one in a series of the two reports of the use of the Borna disease virus (BDV) infection model of neurodevelopmental damage to characterize effects of genetic background on virus-induced neurodevelopmental damage in inbred rat strains, Lewis and Fisher344. The present data demonstrate that neonatal BDV infection produced regional and strain-related alterations in levels of serotonin, norepinephrine and in levels of serotonin turnover at postnatal day 120. Neonatal BDV infection also induced upregulation of hippocampal 5-HT(1a) and cortical 5-HT(2a) receptors in Lewis rats and downregulation of cortical 5-HT(2a) receptors in Fisher344 rats. BDV-associated regional downregulation of D(2) receptors and dopamine transporter sites were noted in Fisher344 rats. In addition to the neurochemical disturbances, neonatal BDV infection induced differential responses to serotonin compounds. While 8-OH-DPAT suppressed virus-enhanced ambulation in BDV-infected Fisher344, fluoxetine inhibited virus-induced hyperactivity in BDV-infected Lewis rats only. The present data provide new insights into the pathogenic events that lead to differential responses to pharmacological treatments in genetically different animals following exposure to the same environmental challenge.
  • |*Nerve Tissue Proteins[MESH]
  • |8-Hydroxy-2-(di-n-propylamino)tetralin/pharmacology[MESH]
  • |Animal Diseases[MESH]
  • |Animals[MESH]
  • |Animals, Newborn[MESH]
  • |Borna Disease/*genetics/physiopathology/virology[MESH]
  • |Brain Chemistry/drug effects/*genetics[MESH]
  • |Brain/drug effects/metabolism/*virology[MESH]
  • |Carrier Proteins/genetics/metabolism[MESH]
  • |Dopamine Plasma Membrane Transport Proteins[MESH]
  • |Dopamine/metabolism[MESH]
  • |Female[MESH]
  • |Fenclonine/pharmacology[MESH]
  • |Fluoxetine/pharmacology[MESH]
  • |Genetic Predisposition to Disease/*genetics[MESH]
  • |Haloperidol/pharmacology[MESH]
  • |Membrane Glycoproteins/genetics/metabolism[MESH]
  • |Membrane Transport Proteins/genetics/metabolism[MESH]
  • |Neurons/drug effects/metabolism/*virology[MESH]
  • |Neurotransmitter Agents/*genetics/metabolism[MESH]
  • |Norepinephrine/metabolism[MESH]
  • |Pregnancy[MESH]
  • |Rats[MESH]
  • |Rats, Inbred F344[MESH]
  • |Rats, Inbred Lew[MESH]
  • |Receptor, Serotonin, 5-HT2A[MESH]
  • |Receptors, Dopamine D2/genetics/metabolism[MESH]
  • |Receptors, Neurotransmitter/drug effects/*genetics/metabolism[MESH]
  • |Receptors, Serotonin, 5-HT1[MESH]
  • |Receptors, Serotonin/genetics/metabolism[MESH]
  • |Serotonin Plasma Membrane Transport Proteins[MESH]
  • |Serotonin/metabolism[MESH]


  • DeepDyve
  • Pubget Overpricing
  • garesp_yesshow ga

    108 1-2.944 2002