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Norepinephrine-induced phasic activity in tail arteries from genetically hypertensive rats
The American Journal of Physiology
|March 1, 1985
Summary
Norepinephrine causes unusual, fluctuating contractions in the arteries of stroke-prone rats. These responses, linked to ion channel changes, highlight unique vascular smooth muscle cell behavior in SHRSP.
Area of Science:
- Cardiovascular Physiology
- Vascular Biology
- Hypertension Research
Background:
- Spontaneously hypertensive stroke-prone (SHRSP) rats exhibit distinct cardiovascular pathologies.
- Understanding arterial smooth muscle function is crucial for hypertension research.
Purpose of the Study:
- To investigate the effects of norepinephrine on contractile force in SHRSP rat tail arteries.
- To compare these responses with those in normotensive Wistar Kyoto (WKY) rats.
- To elucidate the ionic mechanisms underlying norepinephrine-induced contractions in SHRSP.
Main Methods:
- Isometric contractions of isolated tail artery strips from SHRSP and WKY rats were recorded.
- Norepinephrine was applied at varying concentrations (1.8 X 10(-9) to 1.8 X 10(-6) M).
- The effects of various interventions (ouabain, temperature changes, ionic solutions, ion channel blockers) on contractile responses were assessed.
Main Results:
- Norepinephrine induced fluctuating contractile activity in SHRSP arteries, unlike the constant responses in WKY arteries.
- The magnitude and frequency of these phasic responses in SHRSP were dose-dependent.
- These phasic responses were reversed by ouabain, cold temperature, potassium-free solutions, BaCl2, KCl, tetraethylammonium chloride, chloride-free solutions, and D600.
Conclusions:
- Altered calcium and potassium movements across the cell membrane are implicated in the phasic contractile responses to norepinephrine in SHRSP.
- Arterial vascular smooth muscle cell membranes in SHRSP rats display unique functional characteristics.
- This study reveals distinct cellular mechanisms contributing to hypertension in SHRSP models.