HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Does brain histamine contribute to the development of hypertension in spontaneously hypertensive rats?

Abstract
Histaminergic neurons of the brain have been implicated in genetic hypertension. We investigated the effect of inhibition of histamine synthesis by alpha-fluoromethylhistidine (alpha-FMH), the irreversible inhibitor of histidine decarboxylase, on the development and maintenance of hypertension in spontaneously hypertensive rats. Young (3-week-old) and adult (7-week-old) rats were treated with alpha-fluoromethylhistidine for 29 and 13 days, respectively. Treatment of spontaneously hypertensive rats and normotensive Wistar-Kyoto rats with alpha-fluoromethylhistidine led to a pronounced decrease in the histidine decarboxylase activity and in the histamine concentration in the brain (hypothalamus, brainstem, cortex-midbrain). In adult spontaneously hypertensive rats, the development of hypertension was not influenced by alpha-fluoromethylhistidine. In young spontaneously hypertensive rats, alpha-fluoromethylhistidine led to a transient delay in the development of hypertension which was followed by a transient tendency to increased blood pressure. It is concluded that histaminergic neurons of the brain play only a subordinate role, if any at all, in the development of hypertension in spontaneously hypertensive rats.
AuthorsH Prast, A Philippu
JournalNaunyn-Schmiedeberg's archives of pharmacology (Naunyn Schmiedebergs Arch Pharmacol) Vol. 343 Issue 3 Pg. 307-10 (Mar 1991) ISSN: 0028-1298 [Print] Germany
PMID1865929 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Methylhistidines
  • alpha-fluoromethylhistidine
  • Histamine
  • Histidine Decarboxylase
Topics
  • Animals
  • Blood Pressure (drug effects, physiology)
  • Brain (metabolism)
  • Brain Chemistry
  • Brain Stem (metabolism)
  • Cerebral Cortex (metabolism)
  • Histamine (biosynthesis, physiology)
  • Histidine Decarboxylase (antagonists & inhibitors, metabolism)
  • Hypertension (etiology)
  • Hypothalamus (metabolism)
  • Mesencephalon (metabolism)
  • Methylhistidines (pharmacology)
  • Rats
  • Rats, Inbred SHR
  • Rats, Inbred WKY

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: