The Lung–Brain Axis in Ventilator-induced Brain Injury: Enter IL-6

Abstract

Neurological dysfunctionanddeliriummayaffectup to80%ofpatients in the ICUbutare frequentlyunderrecognizedandunderdiagnosed(1). Neurocognitive impairment and even brain structural alterations often persistafter ICUrelease, renderingICU-associatedneurologicaldeficits an important contributor to long-termmorbidity and reduced quality of life in critically ill patients that imposes a significant burden on healthcare systems. In addition topsychological factors, includingposttraumatic stress, depression,or adverse effects afterprolonged sedation, mechanical ventilation has recently emerged as an important contributor to ICU-associated acute and long-term neurological impairment. Epidemiological studies indicate that intubation and positivepressure ventilation increase the incidence of delirium inpatients in the ICU (2). A direct cause–effect relationship for this association was established in preclinical studies, which found altered neuronal activity in the hippocampus and increased hippocampal apoptosis in mechanically ventilated as compared with spontaneously breathing mice (3, 4). Mechanistically, these effects have been attributed to the activation of lung mechanosensors—namely transient receptor potential vanilloid 4 cation channels and purinergic receptors— triggering a local increase in hippocampal dopaminergic signaling that can be attenuated by vagotomy or type-2 dopamine receptor antagonists (3, 4). Yet, apart from vagal afferents, additional “lung–brain axes” acting via the blood route rather than the autonomic nervous systemmay independently or synergistically contribute to ventilator-inducedbrain injury. Inparticular, circulating inflammatory cytokines represent likely candidates for such interorgan communication. In an article published in this issue of the Journal, Sparrow and colleagues (pp. 403–412) now report a critical role for IL-6 in the induction of neuronal injury by mechanical ventilation (5). In anesthetized mice, ventilation with supraclinical tidal volumes (VT) of 35 mL/kg body weight induced neuronal apoptosis in frontal and hippocampal brain regions as evidenced by cleaved caspase 3 staining. In the frontal cortex, this was associated with enhanced immunostaining for three key inflammatory cytokines, namely, IL-6, IL-1b, and TNF, as compared with brain sections from spontaneously breathing mice. Importantly, inhibition of IL-6 signaling by intraperitonealadministrationofantibodiesagainsteither IL-6orIL-6R (IL-6 receptor) attenuated frontal and hippocampal apoptosis and reduced IL-6 and TNF immunostaining in the frontal cortex as compared with saline treated animals. In summary, these results identify inflammatory signaling via IL-6 as a novel and potentially targetable “lung–brain axis” in the induction of ventilator-induced neuronal injury. The concept of an IL-6–mediated lung–brain cross-talk in mechanical ventilation is inkeepingwithabodyofdatahighlighting the releaseofIL-6fromoverventilated lungsandtheassociationof IL-6with neurological impairment. In their landmark paper that established the biotrauma concept of ventilator-induced lung injury, Tremblay and colleagues demonstrated the release of high levels of IL-6 (along with other cytokines, including IL-1b andTNF) that couldbedetected in the bronchoalveolar lavageof isolated rat lungswhen subjected to injurious ventilation (6). In patients, circulating levels of IL-6 have been directly linked to mechanical ventilation strategies in the 2000 ARDSNetwork Trial,whichdemonstrated that lungprotective ventilationwithVTsof 6 mL/kgbodyweightascomparedwithconventionalVTsof12mL/kgnot only decreased 28 daymortality in acute respiratory distress syndrome patients from 39.8 to 31.0 percent, but also reduced circulating IL-6 levels(7).What ismore,highpreoperativeIL-6levelshavebeenfoundto be associated with an increased risk for postoperative delirium in patients. 65 years of age (8). Although IL-6 thus emerges as a likely mediator of ventilation-induced brain injury, several key questions remain. First, in their study, Sparrow and colleagues observed increased BAL fluid levels of IL-6 and IL-6–mediated brain injury in mice ventilated at a VT of 35 mL/kg, a finding that is in keeping with a recent study reporting IL-6 release fromalveolarmacrophages atVTs of 35–40 mL/kg (9). In the era of lung protective ventilation, however, clinically delivered VTs will rarely exceed 20 mL/kg even when considering that up to two thirds of total lung volume may not participate in mechanical ventilation in critically ill patients (10). Notably, the original biotrauma reported elevated IL-6 levels only in bronchoalveolar lavage fluid of rat lungs rigorously ventilated with excessive VTs of 40 mL/kg while IL-6 was virtually undetectable at moderate VTs of 15 mL/kg (6). Although data from the ARDS Network Trial cited above indicate that changes in circulating IL-6 levels may occur in patients at lower VTs (7), it remains to be shown whether IL-6 levels generated by clinically relevant VTs or even under lung protective ventilation will suffice to induce functional or structural neurological deficits. Second, assuming that IL-6 is generated by activated macrophages, neutrophils, and potentially epithelial cells in overventilated alveoli and circulates to the brain via the blood, where it can be neutralized by systemically delivered anti–IL-6 antibodies, the question arises as to how IL-6 exerts its effect on frontal and hippocampal neurons. By immunohistochemical analyses, Sparrow and colleagues detected prominent IL-6 staining in cortical blood vessels, as well as in the brain parenchyma of overventilated mice. This finding suggests that IL-6 signaling crosses the blood-brain barrier, either by direct penetration of the cytokine or by induction of a local inflammatory response. Indeed, tracer studies of radioactively labeled IL-6 show uptake of bloodderived IL-6 into the brain parenchyma of healthy mice (11), yet whether this is the result of active IL-6 transcytosis or IL-6–mediated barrier failure remains unknown. Alternatively, IL-6 has been shown to induce the expression of adhesion molecules in microvessels of the central nervous system (12), thus