Why the study?
Does elevation of intracranial pressure following increased left atrial pressure alter lung fluid balance compared to ICP elevation alone in sheep?
Does elevation of intracranial pressure following increased left atrial pressure alter lung fluid balance compared to ICP elevation alone in sheep?
Increases in protein-rich lymph flow following elevation of intracranial pressure are primarily due to changes in pulmonary microvascular surface area rather than permeability.
Answers are grounded in this paper and cite their sources.
No alteration in lung fluid balance after combined ICP and Pla elevation in sheep; hypothesis-generating for microvascular surface area versus permeability mechanisms.
Elevation of intracranial pressure (ICP; 50-150 Torr) in sheep produces an increase in protein-rich lymph flow (QL) from the lung. This may be attributed to either microvascular permeability changes or increases in filtration surface area through recruitment. To eliminate increases in surface area, we recruited potential filtration beds by increasing left atrial pressure (Pla; 27-35 Torr) prior to elevating ICP in sheep anesthetized with pentobarbital sodium or halothane. Under these conditions, increased pulmonary microvascular permeability would be expected to produce an increased QL, lymphatic protein flux (CL), and plasma clearance of protein (CP). The results of ICP elevation following a period of steady-state Pla hypertension showed no such change in QL, CL or CP (n=8) compared with prior period of increased Pla. ICP elevation alone (n=6) produces a significant increase in CP manifested as an increase in QL (73%), with little change in the lymph-to-plasma ratio of protein concentration. These results suggest that a change in pulmonary microvascular surface area (not permeability) is the primary mechanism underlying increases in protein-rich QL following the elevation of ICP alone.
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Jones et al. (1982) studied this question.
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