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Effects of L-threo-dihydroxyphenylserine on spinal reflexes and decerebrate rigidity in rats.

Abstract
1. The effects of a noradrenaline precursor, L-threo-3,4-dihydroxyphenylserine (L-DOPS), on spinal mono-(MSR) and polysynaptic reflexes (PSR) and decerebrate rigidity, were studied. 2. Although a low dose of L-DOPS (10 mg/kg, i.v.) did not affect MSR or PSR in C1 spinal rats, high doses of L-DOPS (50 and 100 mg/kg, i.v.) moderately enhanced the amplitudes of both MSR and PSR. 3. Clorgyline-HCl (1 mg/kg, i.v.), an MAO inhibitor, enhanced the excitatory effects of low-dose L-DOPS (10 mg/kg, i.v.) on both reflexes. 4. Benserazide-HCl (1 mg/kg, i.v.), an L-aromatic amino acid decarboxylase inhibitor, decreased the pressor effect, but not the stimulatory effects, of L-DOPS (100 mg/kg, i.v.) on MSR and PSR. 5. L-DOPS (300 mg/kg, i.p. or i.d.) did not affect the muscle tone of rigid hindlimbs caused by radio frequency lesioning of the midbrain. 6. These results suggest that the moderate enhancing effects of L-DOPS on MSR and PSR are due to conversion of L-DOPS to noradrenaline in the spinal cord.
AuthorsH Ono, M Tanabe, T Nakamura, N Nagano, H Fukuda
JournalGeneral pharmacology (Gen Pharmacol) Vol. 19 Issue 3 Pg. 369-72 ( 1988) ISSN: 0306-3623 [Print] England
PMID3138156 (Publication Type: Journal Article)
Chemical References
  • Serine
  • Benserazide
  • Droxidopa
  • Clorgyline
Topics
  • Animals
  • Benserazide (pharmacology)
  • Blood Pressure (drug effects)
  • Clorgyline (pharmacology)
  • Decerebrate State (physiopathology)
  • Droxidopa (antagonists & inhibitors, pharmacology)
  • Male
  • Motor Activity (drug effects)
  • Rats
  • Rats, Inbred Strains
  • Reflex (drug effects)
  • Serine (analogs & derivatives)
  • Spinal Cord (drug effects)

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