Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1980-9-26
pubmed:abstractText
In unanesthetized sponatneously hypertensive rats (SHR), naloxone (0.5--2 mg/kg ip.) or naltrexone (2 mg/kg) inhibited the hypotension and bradycardia produced by clonidine (5--20 micrograms/kg iv.). Chronic treatment of SHR with clonidine (3 x 20 micrograms/kg/day orally for 12 days) reduced blood pressure and heart rate and these effects were acutely reversed by a single injection of naloxone. Naloxone also reversed the hypotension produced by a single injection of alpha-methyldopa (50--300 mg/kg ip.). In pentobarbital-anesthetized SHR, the hypotension and bradycardia produced by 5 micrograms/kg of clonidine were inhibited either by naloxone (2 mg/kg) or by yohimbine (1 mg/kg ip.). Morphine (0.33 mg/kg iv.) also reduced blood pressure and heart rate in these animals but these effects were only antagonized by naloxone and not by yohimbine. In conscious and anesthetized normotensive Wistar Kyoto rats, the reduction in blood pressure and heart rate by clonidine or alpha-methyldopa were smaller than in SHR, and these effects were not influenced by naloxone. These results confirm and extend earlier observations and suggest the existence of an "opioidergic" component in the antihypertensive action of central alpha adrenoceptor stimulants in SHR. They also show that a similar mechanism is either absent or inactive in the normotensive Wistar Kyoto rats.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0022-3565
pubmed:author
pubmed:issnType
Print
pubmed:volume
214
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
203-8
pubmed:dateRevised
2003-11-14
pubmed:meshHeading
pubmed-meshheading:6248627-Anesthesia, pubmed-meshheading:6248627-Animals, pubmed-meshheading:6248627-Blood Pressure, pubmed-meshheading:6248627-Clonidine, pubmed-meshheading:6248627-Dose-Response Relationship, Drug, pubmed-meshheading:6248627-Drug Interactions, pubmed-meshheading:6248627-Endorphins, pubmed-meshheading:6248627-Heart Rate, pubmed-meshheading:6248627-Hypertension, pubmed-meshheading:6248627-Male, pubmed-meshheading:6248627-Methyldopa, pubmed-meshheading:6248627-Morphine, pubmed-meshheading:6248627-Naloxone, pubmed-meshheading:6248627-Naltrexone, pubmed-meshheading:6248627-Rats, pubmed-meshheading:6248627-Receptors, Adrenergic, pubmed-meshheading:6248627-Receptors, Adrenergic, alpha, pubmed-meshheading:6248627-Receptors, Opioid, pubmed-meshheading:6248627-Time Factors, pubmed-meshheading:6248627-Yohimbine
pubmed:year
1980
pubmed:articleTitle
Possible role of an endogenous opiate in the cardiovascular effects of central alpha adrenoceptor stimulation in spontaneously hypertensive rats.
pubmed:publicationType
Journal Article