Effect of mobile telephony on blood-brain barrier permeability in the fetal mouse brain
To study the effect of mobile telephone exposure on blood-brain barrier (BBB) permeability in the immature brain. Using a purpose-designed exposure system at 900 MHz, pregnant mice were given a single, far-field, whole body exposure at a specific absorption rate of 4W/kg for 60min/day from day 1 to...
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Published in | Pathology Vol. 38; no. 1; pp. 63 - 65 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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London
Elsevier B.V
01.02.2006
Informa UK Ltd Taylor and Francis |
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Abstract | To study the effect of mobile telephone exposure on blood-brain barrier (BBB) permeability in the immature brain.
Using a purpose-designed exposure system at 900 MHz, pregnant mice were given a single, far-field, whole body exposure at a specific absorption rate of 4W/kg for 60min/day from day 1 to day 19 of gestation. Pregnant control mice were sham-exposed or freely mobile in a cage without further restraint and a positive control group with cadmium-induced BBB damage was also included. Immediately prior to parturition on gestational day 19, fetal heads were collected, fixed in Bouin’s fixative and paraffin embedded. Disruption of BBB integrity was detected immunohistochemically using endogenous albumin as a vascular tracer in cerebral cortex, thalamus, basal ganglia, hippocampus, cerebellum, midbrain and medulla.
No albumin extravasation was found in exposed or control brains.
In this animal model, whole of gestation exposure to global system for mobile communication-like radiofrequency fields did not produce any increase in vascular permeability in the fetal brain regions studied using endogenous albumin as a light microscopic immunohistochemical marker. |
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AbstractList | Aims: To study the effect of mobile telephone exposure on blood-brain barrier (BBB) permeability in the immature brain. Methods: Using a purpose-designed exposure system at 900 MHz, pregnant mice were given a single, far-field, whole body exposure at a specific absorption rate of 4 W/kg for 60 min/day from day 1 to day 19 of gestation. Pregnant control mice were sham-exposed or freely mobile in a cage without further restraint and a positive control group with cadmium-induced BBB damage was also included. Immediately prior to parturition on gestational day 19, fetal heads were collected, fixed in Bouin's fixative and paraffin embedded. Disruption of BBB integrity was detected immunohistochemically using endogenous albumin as a vascular tracer in cerebral cortex, thalamus, basal ganglia, hippocampus, cerebellum, midbrain and medulla. Results: No albumin extravasation was found in exposed or control brains. Conclusion: In this animal model, whole of gestation exposure to global system for mobile communication-like radiofrequency fields did not produce any increase in vascular permeability in the fetal brain regions studied using endogenous albumin as a light microscopic immunohistochemical marker. To study the effect of mobile telephone exposure on blood-brain barrier (BBB) permeability in the immature brain. Using a purpose-designed exposure system at 900 MHz, pregnant mice were given a single, far-field, whole body exposure at a specific absorption rate of 4 W/kg for 60 min/day from day 1 to day 19 of gestation. Pregnant control mice were sham-exposed or freely mobile in a cage without further restraint and a positive control group with cadmium-induced BBB damage was also included. Immediately prior to parturition on gestational day 19, fetal heads were collected, fixed in Bouin's fixative and paraffin embedded. Disruption of BBB integrity was detected immunohistochemically using endogenous albumin as a vascular tracer in cerebral cortex, thalamus, basal ganglia, hippocampus, cerebellum, midbrain and medulla. No albumin extravasation was found in exposed or control brains. In this animal model, whole of gestation exposure to global system for mobile communication-like radiofrequency fields did not produce any increase in vascular permeability in the fetal brain regions studied using endogenous albumin as a light microscopic immunohistochemical marker. Aims: To study the effect of mobile telephone exposure on blood-brain barrier (BBB) permeability in the immature brain. Methods: Using a purpose-designed exposure system at 900 MHz, pregnant mice were given a single, far-field, whole body exposure at a specific absorption rate of 4 W kg for 60 min day from day 1 to day 19 of gestation. Pregnant control mice were sham-exposed or freely mobile in a cage without further restraint and a positive control group with cadmium-induced BBB damage was also included. Immediately prior to parturition on gestational day 19, fetal heads were collected, fixed in Bouin's fixative and paraffin embedded. Disruption of BBB integrity was detected immunohistochemically using endogenous albumin as a vascular tracer in cerebral cortex, thalamus, basal ganglia, hippocampus, cerebellum, midbrain and medulla. Results: No albumin extravasation was found in exposed or control brains. Conclusion: In this animal model, whole of gestation exposure to global system for mobile communication-like radiofrequency fields did not produce any increase in vascular permeability in the fetal brain regions studied using endogenous albumin as a light microscopic immunohistochemical marker. AIMSTo study the effect of mobile telephone exposure on blood-brain barrier (BBB) permeability in the immature brain.METHODSUsing a purpose-designed exposure system at 900 MHz, pregnant mice were given a single, far-field, whole body exposure at a specific absorption rate of 4 W/kg for 60 min/day from day 1 to day 19 of gestation. Pregnant control mice were sham-exposed or freely mobile in a cage without further restraint and a positive control group with cadmium-induced BBB damage was also included. Immediately prior to parturition on gestational day 19, fetal heads were collected, fixed in Bouin's fixative and paraffin embedded. Disruption of BBB integrity was detected immunohistochemically using endogenous albumin as a vascular tracer in cerebral cortex, thalamus, basal ganglia, hippocampus, cerebellum, midbrain and medulla.RESULTSNo albumin extravasation was found in exposed or control brains.CONCLUSIONIn this animal model, whole of gestation exposure to global system for mobile communication-like radiofrequency fields did not produce any increase in vascular permeability in the fetal brain regions studied using endogenous albumin as a light microscopic immunohistochemical marker. To study the effect of mobile telephone exposure on blood-brain barrier (BBB) permeability in the immature brain. Using a purpose-designed exposure system at 900 MHz, pregnant mice were given a single, far-field, whole body exposure at a specific absorption rate of 4W/kg for 60min/day from day 1 to day 19 of gestation. Pregnant control mice were sham-exposed or freely mobile in a cage without further restraint and a positive control group with cadmium-induced BBB damage was also included. Immediately prior to parturition on gestational day 19, fetal heads were collected, fixed in Bouin’s fixative and paraffin embedded. Disruption of BBB integrity was detected immunohistochemically using endogenous albumin as a vascular tracer in cerebral cortex, thalamus, basal ganglia, hippocampus, cerebellum, midbrain and medulla. No albumin extravasation was found in exposed or control brains. In this animal model, whole of gestation exposure to global system for mobile communication-like radiofrequency fields did not produce any increase in vascular permeability in the fetal brain regions studied using endogenous albumin as a light microscopic immunohistochemical marker. |
Author | Finnie, John W. Kuchel, Timothy R. Manavis, Jim Blumbergs, Peter C. Cai, Zhao |
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Keywords | BBB RF fetal brain SAR Mobile telephony murine model BBB permeability Animal model Rodentia Central nervous system Permeability Blood brain barrier Encephalon Vertebrata Anatomic pathology Mammalia Mouse Animal Fetus |
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References | Hossmann, Hermann (bib0010) 2003; 24 Altman, Bayer (bib0070) 1995 (bib0015) 2003 (bib0020) June 9-10 2004 Rodier (bib0025) 1980; 22 Finnie, Blumbergs, Manavis (bib0045) 2002; 34 (bib0060) 1992 Ironside, Pickard (bib0035) 2002 Hardy (bib0055) 2004 Dziegielewska, Saunders (bib0075) 1988 Bauer, Bauer, Lametschwandtner (bib0080) 1993; 75 (bib0005) 2004 Kinney, Armstrong (bib0030) 2002 Finnie, Blumbergs, Manavis (bib0040) 2001; 33 Finnie, Blumbergs (bib0050) 2004; 34 Radovsky, Mahler (bib0085) 1999 Webster, Valois (bib0065) 1981; 40 Hossmann (10.1080/00313020500459607_bib0010) 2003; 24 Rodier (10.1080/00313020500459607_bib0025) 1980; 22 Finnie (10.1080/00313020500459607_bib0040) 2001; 33 Webster (10.1080/00313020500459607_bib0065) 1981; 40 Kinney (10.1080/00313020500459607_bib0030) 2002 Altman (10.1080/00313020500459607_bib0070) 1995 Finnie (10.1080/00313020500459607_bib0045) 2002; 34 Hardy (10.1080/00313020500459607_bib0055) 2004 Radovsky (10.1080/00313020500459607_bib0085) 1999 (10.1080/00313020500459607_bib0005) 2004 Bauer (10.1080/00313020500459607_bib0080) 1993; 75 Dziegielewska (10.1080/00313020500459607_bib0075) 1988 (10.1080/00313020500459607_bib0015) 2003 Ironside (10.1080/00313020500459607_bib0035) 2002 Finnie (10.1080/00313020500459607_bib0050) 2004; 34 (10.1080/00313020500459607_bib0060) 1992 (10.1080/00313020500459607_bib0020) 2004 |
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Snippet | To study the effect of mobile telephone exposure on blood-brain barrier (BBB) permeability in the immature brain.
Using a purpose-designed exposure system at... Aims: To study the effect of mobile telephone exposure on blood-brain barrier (BBB) permeability in the immature brain. Methods: Using a purpose-designed... Aims: To study the effect of mobile telephone exposure on blood-brain barrier (BBB) permeability in the immature brain. Methods: Using a purpose-designed... AIMSTo study the effect of mobile telephone exposure on blood-brain barrier (BBB) permeability in the immature brain.METHODSUsing a purpose-designed exposure... |
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SubjectTerms | Albumins - analysis Animals BBB permeability Biological and medical sciences Blood-Brain Barrier - embryology Blood-Brain Barrier - pathology Blood-Brain Barrier - physiology Brain - embryology Brain - pathology Cadmium - administration & dosage Cell Membrane Permeability - drug effects Cell Membrane Permeability - physiology Cell Phone Cerebellum - embryology Cerebellum - pathology Cerebral Cortex - embryology Cerebral Cortex - pathology Female fetal brain Hippocampus - embryology Hippocampus - pathology Immunohistochemistry Investigative techniques, diagnostic techniques (general aspects) Medical sciences Mesencephalon - embryology Mesencephalon - pathology Mice Mice, Inbred BALB C Mobile telephony Models, Animal murine model Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Pregnancy Prenatal Exposure Delayed Effects - pathology Radio Waves - adverse effects Thalamus - embryology Thalamus - pathology |
Title | Effect of mobile telephony on blood-brain barrier permeability in the fetal mouse brain |
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