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β-amyloid infusion into lateral ventricle alters behavioral thermoregulation and attenuates acquired heat tolerance in rats

We investigated behavioral thermoregulatory function and acquired heat tolerance of β-amyloid (Aβ)-infused rats. Male Wistar rats were anesthetized and implanted in the intraperitoneal cavity with a temperature transmitter. Aβ peptide (4.9–5.5 nmol) was dissolved in a solvent of 35% acetonitrile and...

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Autores principales: Matsuzaki, Kentaro, Katakura, Masanori, Sugimoto, Naotoshi, Hara, Toshiko, Hashimoto, Michio, Shido, Osamu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4843902/
https://www.ncbi.nlm.nih.gov/pubmed/27227055
http://dx.doi.org/10.1080/23328940.2015.1044635
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author Matsuzaki, Kentaro
Katakura, Masanori
Sugimoto, Naotoshi
Hara, Toshiko
Hashimoto, Michio
Shido, Osamu
author_facet Matsuzaki, Kentaro
Katakura, Masanori
Sugimoto, Naotoshi
Hara, Toshiko
Hashimoto, Michio
Shido, Osamu
author_sort Matsuzaki, Kentaro
collection PubMed
description We investigated behavioral thermoregulatory function and acquired heat tolerance of β-amyloid (Aβ)-infused rats. Male Wistar rats were anesthetized and implanted in the intraperitoneal cavity with a temperature transmitter. Aβ peptide (4.9–5.5 nmol) was dissolved in a solvent of 35% acetonitrile and 0.1% trifluoroacetic acid (pH 2.0). The solvent was used as the vehicle. An osmotic pump contained 234 ± 13.9 μl of Aβ solution was subcutaneously implanted in the back and was cannulated into the left cerebral ventricle. Moreover, 0.5 µg of AlCl(3) was injected into the right cerebral ventricle with a micro syringe pump (Aβ-infused rats). The solvent-infused rats were used as control rats (CN rats). After 2 weeks, rats were placed in a thermal gradient and their intra-abdominal temperature (T(ab)) and their ambient temperatures (T(a)) selected (T(s)) were measured for 3 consecutive days. In an additional study, rats were kept at a T(a) of 32°C for 4 weeks to attain heat acclimation. Then, rats were subjected to a heat tolerance test, i.e. they were exposed to a T(a) of 36°C for 160 min. Although there were clear day-night variations of T(s) and T(ab) in CN rats, patterns were significantly abolished in Aβ-infused rats. Moreover, heat tolerance obtained by heat acclimation was attenuated in Aβ-infused rats. These results suggest that Aβ-infusion in the lateral ventricle modifies behavioral thermoregulation and lowers an ability to acclimate to heat in rats.
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spelling pubmed-48439022016-05-25 β-amyloid infusion into lateral ventricle alters behavioral thermoregulation and attenuates acquired heat tolerance in rats Matsuzaki, Kentaro Katakura, Masanori Sugimoto, Naotoshi Hara, Toshiko Hashimoto, Michio Shido, Osamu Temperature (Austin) Priority Report We investigated behavioral thermoregulatory function and acquired heat tolerance of β-amyloid (Aβ)-infused rats. Male Wistar rats were anesthetized and implanted in the intraperitoneal cavity with a temperature transmitter. Aβ peptide (4.9–5.5 nmol) was dissolved in a solvent of 35% acetonitrile and 0.1% trifluoroacetic acid (pH 2.0). The solvent was used as the vehicle. An osmotic pump contained 234 ± 13.9 μl of Aβ solution was subcutaneously implanted in the back and was cannulated into the left cerebral ventricle. Moreover, 0.5 µg of AlCl(3) was injected into the right cerebral ventricle with a micro syringe pump (Aβ-infused rats). The solvent-infused rats were used as control rats (CN rats). After 2 weeks, rats were placed in a thermal gradient and their intra-abdominal temperature (T(ab)) and their ambient temperatures (T(a)) selected (T(s)) were measured for 3 consecutive days. In an additional study, rats were kept at a T(a) of 32°C for 4 weeks to attain heat acclimation. Then, rats were subjected to a heat tolerance test, i.e. they were exposed to a T(a) of 36°C for 160 min. Although there were clear day-night variations of T(s) and T(ab) in CN rats, patterns were significantly abolished in Aβ-infused rats. Moreover, heat tolerance obtained by heat acclimation was attenuated in Aβ-infused rats. These results suggest that Aβ-infusion in the lateral ventricle modifies behavioral thermoregulation and lowers an ability to acclimate to heat in rats. Taylor & Francis 2015-06-03 /pmc/articles/PMC4843902/ /pubmed/27227055 http://dx.doi.org/10.1080/23328940.2015.1044635 Text en © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Priority Report
Matsuzaki, Kentaro
Katakura, Masanori
Sugimoto, Naotoshi
Hara, Toshiko
Hashimoto, Michio
Shido, Osamu
β-amyloid infusion into lateral ventricle alters behavioral thermoregulation and attenuates acquired heat tolerance in rats
title β-amyloid infusion into lateral ventricle alters behavioral thermoregulation and attenuates acquired heat tolerance in rats
title_full β-amyloid infusion into lateral ventricle alters behavioral thermoregulation and attenuates acquired heat tolerance in rats
title_fullStr β-amyloid infusion into lateral ventricle alters behavioral thermoregulation and attenuates acquired heat tolerance in rats
title_full_unstemmed β-amyloid infusion into lateral ventricle alters behavioral thermoregulation and attenuates acquired heat tolerance in rats
title_short β-amyloid infusion into lateral ventricle alters behavioral thermoregulation and attenuates acquired heat tolerance in rats
title_sort β-amyloid infusion into lateral ventricle alters behavioral thermoregulation and attenuates acquired heat tolerance in rats
topic Priority Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4843902/
https://www.ncbi.nlm.nih.gov/pubmed/27227055
http://dx.doi.org/10.1080/23328940.2015.1044635
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