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Pial vessel caliber and cerebral blood flow become dissociated during ischemia-reperfusion in cats

E Tasdemiroglu1, R Macfarlane, E P Wei

  • 1Neurology Service, Massachusetts General Hospital, Harvard Medical School, Boston 02114.

Insights

Following cerebral ischemia, pial arterioles dilated significantly, but this did not fully restore cerebral blood flow (CBF). Parenchymal vessels, not pial ones, likely regulate CBF during reperfusion.

Area of Science:

  • Neuroscience
  • Cerebrovascular Physiology
  • Ischemia-Reperfusion Research

Background:

  • Global cerebral ischemia can lead to significant alterations in cerebral blood flow (CBF) and cerebrovascular resistance.
  • Understanding the role of pial arterioles in regulating CBF during reperfusion is crucial for developing effective treatments.

Purpose of the Study:

  • To investigate the relationship between pial arteriolar caliber and cerebral blood flow (CBF) during reperfusion after global cerebral ischemia.
  • To determine the contribution of pial arterioles to the restoration of CBF and cerebrovascular resistance post-ischemia.

Main Methods:

  • Global cerebral ischemia was induced in cats via four-vessel occlusion and hypotension.
  • Reperfusion was maintained for up to 120 minutes.
  • Cerebral blood flow (CBF) was measured using radiolabeled microsphere injection.
  • Pial arteriolar caliber was assessed using the closed cranial window technique.

Main Results:

  • CBF increased dramatically (588%) 30 minutes post-reperfusion, with concurrent pial arteriolar dilation (172%).
  • At 60 and 120 minutes, CBF returned to near baseline, while pial arterioles remained dilated (133% and 115%, respectively).
  • Total cerebrovascular resistance normalized by 45 minutes, despite persistent pial arteriolar dilation.

Conclusions:

  • Pial arteriolar dilation alone does not fully explain normal blood flow restoration after ischemia-induced hyperemia.
  • Increased resistance within parenchymal vessels, rather than pial vessels, is likely responsible for regulating CBF during the post-hyperemic phase.
  • Further research is needed to determine if obstruction or vasoconstriction causes increased resistance in intraparenchymal vessels.

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