Impact of ether anesthesia on the hypophyseal content of oxytocin neurophysin I and II: A comparative study with ketamine in the rat

The effect of anesthetic stress on the major hormones of the posterior pituitary (PP), such as oxytocin (OT), oxytocin-neurophysin (OTNP-I) and its metabolic product, OTNP-II, was studied. Rats were treated with either a combination of atropine (0.87 mg/kg) and diphenylhydantoin (85 mg/kg) and then...

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Veröffentlicht in:Life sciences (1973) 1991, Vol.49 (19), p.1391-1397
1. Verfasser: Zierer, Rainer
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description The effect of anesthetic stress on the major hormones of the posterior pituitary (PP), such as oxytocin (OT), oxytocin-neurophysin (OTNP-I) and its metabolic product, OTNP-II, was studied. Rats were treated with either a combination of atropine (0.87 mg/kg) and diphenylhydantoin (85 mg/kg) and then anesthetized with ketamine (42 mg/kg) or were directly anesthetized with diethyl-ether, and then killed. Controls were killed with a laboratory guillotine. Our study revealed that 1.) animals killed with a guillotine or being medicated with our drug combination prior to sacrifice had similar concentrations of OT, OTNP-I and OTNP-II per PP and ml of blood; 2.) animals anesthetized with ether prior to sacrifice had a decreased concentration of neuropeptides per PP; the blood concentration of OT was 1.6 times higher than in animals treated with the drug combination or killed directly with a guillotine. In addition plasma concentrations of OTNP-I and OTNP-II were above the baseline. We conclude that ether is not an adequate anesthetic for studying the neurophysins from the PP in vivo. Treatment of animals with atropine and diphenylhydantoin in combination with ketamine does not alter the profile of the major hormones from the PP during anesthetic stress.
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Rats were treated with either a combination of atropine (0.87 mg/kg) and diphenylhydantoin (85 mg/kg) and then anesthetized with ketamine (42 mg/kg) or were directly anesthetized with diethyl-ether, and then killed. Controls were killed with a laboratory guillotine. Our study revealed that 1.) animals killed with a guillotine or being medicated with our drug combination prior to sacrifice had similar concentrations of OT, OTNP-I and OTNP-II per PP and ml of blood; 2.) animals anesthetized with ether prior to sacrifice had a decreased concentration of neuropeptides per PP; the blood concentration of OT was 1.6 times higher than in animals treated with the drug combination or killed directly with a guillotine. In addition plasma concentrations of OTNP-I and OTNP-II were above the baseline. We conclude that ether is not an adequate anesthetic for studying the neurophysins from the PP in vivo. 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Rats were treated with either a combination of atropine (0.87 mg/kg) and diphenylhydantoin (85 mg/kg) and then anesthetized with ketamine (42 mg/kg) or were directly anesthetized with diethyl-ether, and then killed. Controls were killed with a laboratory guillotine. Our study revealed that 1.) animals killed with a guillotine or being medicated with our drug combination prior to sacrifice had similar concentrations of OT, OTNP-I and OTNP-II per PP and ml of blood; 2.) animals anesthetized with ether prior to sacrifice had a decreased concentration of neuropeptides per PP; the blood concentration of OT was 1.6 times higher than in animals treated with the drug combination or killed directly with a guillotine. In addition plasma concentrations of OTNP-I and OTNP-II were above the baseline. We conclude that ether is not an adequate anesthetic for studying the neurophysins from the PP in vivo. Treatment of animals with atropine and diphenylhydantoin in combination with ketamine does not alter the profile of the major hormones from the PP during anesthetic stress.</description><subject>Analysis of Variance</subject><subject>Anesthesia</subject><subject>Anesthetics. Neuromuscular blocking agents</subject><subject>Animals</subject><subject>Arginine Vasopressin - blood</subject><subject>Atropine - administration &amp; dosage</subject><subject>Biological and medical sciences</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Ether - pharmacology</subject><subject>Ketamine - pharmacology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neuropharmacology</subject><subject>Neurophysins - blood</subject><subject>Neurophysins - metabolism</subject><subject>Oxytocin - blood</subject><subject>Oxytocin - metabolism</subject><subject>Pharmacology. Drug treatments</subject><subject>Phenytoin - administration &amp; dosage</subject><subject>Pituitary Gland, Posterior - drug effects</subject><subject>Pituitary Gland, Posterior - metabolism</subject><subject>Random Allocation</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><issn>0024-3205</issn><issn>1879-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtv1DAUhS0EKkPhH4DkBUJlEbDHjyRdIFUVj0iV2IC6tDz2jcaQ2MF2Ctn3h-OZjMoOeeErne8c3XsQeknJO0qofE_IlldsS8RFS9-2hLWkun2ENrSp24pIRh-jzQPyFD1L6QchRIianaEz2nLGudig-26ctMk49BjyHiLWHlIZktM4eFwmvF-mMO2XBHrAJvgM_oiHP0sOxnnsYY5HoMxd8VvcdZf4qrAlOurs7gCnPNsF_3Z5j39C1qPzgN0aX4jn6EmvhwQvTv85-v7p47frL9XN18_d9dVNZRihuRLMCNsbANJrYbntey55zc2uqbWURhsppGyK0HC6k1JYytqm5lqTHWjOOTtHb9bcKYZfc7lTjS4ZGIZydJiTqrdclCcLyFfQxJBShF5N0Y06LooSdShfHZpVh2ZVS9WxfHVbbK9O-fNuBPvPtLZd9NcnXSejhz5qb1x6wHjbCCJYwT6sGJQu7hxElYwDb8C6CCYrG9z_9_gLt2uiVg</recordid><startdate>1991</startdate><enddate>1991</enddate><creator>Zierer, Rainer</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>1991</creationdate><title>Impact of ether anesthesia on the hypophyseal content of oxytocin neurophysin I and II: A comparative study with ketamine in the rat</title><author>Zierer, Rainer</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c301t-53c5dfcee0fa5d4dff46474cb87a66cac65668d4d841b665d139874aa0bea4443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Analysis of Variance</topic><topic>Anesthesia</topic><topic>Anesthetics. Neuromuscular blocking agents</topic><topic>Animals</topic><topic>Arginine Vasopressin - blood</topic><topic>Atropine - administration &amp; dosage</topic><topic>Biological and medical sciences</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Ether - pharmacology</topic><topic>Ketamine - pharmacology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neuropharmacology</topic><topic>Neurophysins - blood</topic><topic>Neurophysins - metabolism</topic><topic>Oxytocin - blood</topic><topic>Oxytocin - metabolism</topic><topic>Pharmacology. Drug treatments</topic><topic>Phenytoin - administration &amp; dosage</topic><topic>Pituitary Gland, Posterior - drug effects</topic><topic>Pituitary Gland, Posterior - metabolism</topic><topic>Random Allocation</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zierer, Rainer</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Life sciences (1973)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zierer, Rainer</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of ether anesthesia on the hypophyseal content of oxytocin neurophysin I and II: A comparative study with ketamine in the rat</atitle><jtitle>Life sciences (1973)</jtitle><addtitle>Life Sci</addtitle><date>1991</date><risdate>1991</risdate><volume>49</volume><issue>19</issue><spage>1391</spage><epage>1397</epage><pages>1391-1397</pages><issn>0024-3205</issn><eissn>1879-0631</eissn><coden>LIFSAK</coden><abstract>The effect of anesthetic stress on the major hormones of the posterior pituitary (PP), such as oxytocin (OT), oxytocin-neurophysin (OTNP-I) and its metabolic product, OTNP-II, was studied. Rats were treated with either a combination of atropine (0.87 mg/kg) and diphenylhydantoin (85 mg/kg) and then anesthetized with ketamine (42 mg/kg) or were directly anesthetized with diethyl-ether, and then killed. Controls were killed with a laboratory guillotine. Our study revealed that 1.) animals killed with a guillotine or being medicated with our drug combination prior to sacrifice had similar concentrations of OT, OTNP-I and OTNP-II per PP and ml of blood; 2.) animals anesthetized with ether prior to sacrifice had a decreased concentration of neuropeptides per PP; the blood concentration of OT was 1.6 times higher than in animals treated with the drug combination or killed directly with a guillotine. In addition plasma concentrations of OTNP-I and OTNP-II were above the baseline. We conclude that ether is not an adequate anesthetic for studying the neurophysins from the PP in vivo. 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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Analysis of Variance
Anesthesia
Anesthetics. Neuromuscular blocking agents
Animals
Arginine Vasopressin - blood
Atropine - administration & dosage
Biological and medical sciences
Chromatography, High Pressure Liquid
Ether - pharmacology
Ketamine - pharmacology
Male
Medical sciences
Neuropharmacology
Neurophysins - blood
Neurophysins - metabolism
Oxytocin - blood
Oxytocin - metabolism
Pharmacology. Drug treatments
Phenytoin - administration & dosage
Pituitary Gland, Posterior - drug effects
Pituitary Gland, Posterior - metabolism
Random Allocation
Rats
Rats, Inbred Strains
title Impact of ether anesthesia on the hypophyseal content of oxytocin neurophysin I and II: A comparative study with ketamine in the rat
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