Biomedical subjects

Courtney L Robertson

Publications and source records attributed to Courtney L Robertson.

6 recordsLinked to original sources

PubMed2006

The potential role of mitochondria in pediatric traumatic brain injury.

Mitochondria play a central role in cerebral energy metabolism, intracellular calcium homeostasis and reactive oxygen species generation and detoxification. Following traumatic brain injury (TBI), the degree of mitochondrial injury or dysfunction can be an important determinant of cell survival or death. Literature would suggest that brain mitochondria from the developing brain are very different from those from mature animals. Therefore, aspects of developmental differences in the mitochondrial response to TBI can make the immature brain more vulnerable to traumatic injury. This review will focus on four main areas of secondary injury after pediatric TBI, including excitotoxicity, oxidative stress, alterations in energy metabolism and cell death pathways. Specifically, we will describe what is known about developmental differences in mitochondrial function in these areas, in both the normal, physiologic state and the pathologic state after pediatric TBI. The ability to identify and target aspects of mitochondrial dysfunction could lead to novel neuroprotective therapies for infants and children after severe TBI.

Aging↗

PubMed2005

Physiologic progesterone reduces mitochondrial dysfunction and hippocampal cell loss after traumatic brain injury in female rats.

Growing literature suggests important sex-based differences in outcome following traumatic brain injury (TBI) in animals and humans. Progesterone has emerged as a key hormone involved in many potential neuroprotective pathways after acute brain injury and may be responsible for some of these differences. Many studies have utilized supraphysiologic levels of post-traumatic progesterone to reverse pathologic processes after TBI, but few studies have focused on the role of endogenous physiologic levels of progesterone in neuroprotection. We hypothesized that progesterone at physiologic serum levels would be neuroprotective in female rats after TBI and that progesterone would reverse early mitochondrial dysfunction seen in this model. Female, Sprague-Dawley rats were ovariectomized and implanted with silastic capsules containing either low or high physiologic range progesterone at 7 days prior to TBI. Control rats received ovariectomy with implants containing no hormone. Rats underwent controlled cortical impact to the left parietotemporal cortex and were evaluated for evidence of early mitochondrial dysfunction (1 h) and delayed hippocampal neuronal injury and cortical tissue loss (7 days) after injury. Progesterone in the low physiologic range reversed the early postinjury alterations seen in mitochondrial respiration and reduced hippocampal neuronal loss in both the CA1 and CA3 subfields. Progesterone in the high physiologic range had a more limited pattern of hippocampal neuronal preservation in the CA3 region only. Neither progesterone dose significantly reduced cortical tissue loss. These findings have implications in understanding the sex-based differences in outcome following acute brain injury.

Animals↗

PubMed2005

Prospective assessment of guidelines for determining appropriate depth of endotracheal tube placement in children.

OBJECTIVE: To determine whether multiplying the internal diameter of the endotracheal tube (ETT) by 3 (3x ETT size) is a reliable method for determining correct depth of oral ETT placement in the pediatric population. DESIGN: Prospective, observational. SETTING: University-affiliated, 12-bed pediatric intensive care unit. PATIENTS: Orally intubated pediatric intensive care unit patients of < or =12 yrs of age. INTERVENTIONS: Demographics, ETT size, and depth of ETT placement measured from the lip were obtained. Correct placement, defined as the tip of the ETT below the thoracic inlet and > or =0.5 cm above the carina, was determined by chest radiograph. MEASUREMENTS AND MAIN RESULTS: Suggested ETT size based on the Pediatric Advanced Life Support (PALS) age-based formula and the Broselow tape-length-based guidelines were determined. A total of 174 of 226 ETTs (77%) were correctly positioned. If practitioners utilized the 3x ETT size for the actual tubes chosen, 170 of 226 (75%) would have been accurately placed. More accurate were the 3x PALS-based ETT size (81%) and 3x Broselow-suggested ETT size (85%). The use of the Broselow ETTs to determine the depth would have led to a significantly improved ETT position (p = .009) compared with the actual ETT. CONCLUSION: The commonly used formula of 3x tube size for ETT depth in children results in 15-25% malpositioned tubes. Practitioners can improve the reliability of this formula by utilizing the recommended ETT size as suggested by the Broselow tape. A more reliable method is necessary to avoid ETT malposition.

Age Factors↗

PubMed2005

Synthes Award for Resident Research on Brain and Craniofacial Injury: normoxic ventilatory resuscitation after controlled cortical impact reduces peroxynitrite-mediated protein nitration in the hippocampus.

Resuscitation with 100% ventilatory oxygen is routinely initiated after severe traumatic brain injury (TBI). Despite the objective to improve oxygenation of the injured brain, there are concerns about the increased production of reactive oxygen species (ROS), which can lead to further neuronal damage. 3-nitrotyrosine (3-NT), the product of peroxynitrite-meditated tyrosine residue nitration, has been used as a marker for ROS-induced oxidative damage to proteins. We hypothesized that posttraumatic resuscitation with hyperoxic ventilation with a fraction of inspired oxygen (Fio2, 100%) results in increased ROS-induced damage to proteins compared with resuscitation with normoxic ventilation or room air (Fio2, 21%). Male Sprague-Dawley rats underwent controlled cortical impact (CCI) and were resuscitated with either normoxic or hyperoxic ventilation for 1 hour after injury (n = 5 per group). Sham-operated control groups received 1 hour of normoxic or hyperoxic ventilation without CCI (n = 4-5 per group). Twenty-four hours after injury, rats were perfused with fixative, and hippocampi were evaluated for levels of 3-NT immunostaining. In a second experiment, for a delayed assessment of neuronal survival, another set of rats similarly underwent CCI and normoxic or hyperoxic ventilation for 1 hour (n = 4 per group), and a sham-operated group was used as a control (n = 4). One week after injury, neuronal cell counts and abnormal cell quantification were performed after staining with the neuron-specific NeuN antibody. Quantification of 3-NT staining revealed significantly increased levels in the ipsilateral hippocampus in the hyperoxic CCI group. The normoxic group showed a 51.0% reduction of staining in CA1 when compared with those rats resuscitated with hyperoxia and a 50.8% reduction in CA3 (both P < 0.05). There was no significant difference in staining between the injured normoxic group and the sham-operated groups. In the delayed analysis of neuronal survival, although neuronal counts were reduced in the hippocampus on the injured side in both injured groups, there was no significant difference between hyperoxic and normoxic groups. Similarly, abnormal cell counts were not significantly different between groups.

Animals↗

PubMed2004

Mitochondrial response to calcium in the developing brain.

Developmental differences in mitochondrial content and metabolic enzyme activities have been defined, but less is understood about the responses of brain mitochondria to stressful stimuli during development. Cerebral mitochondrial response to high Ca(2+) loads after brain injury is a critical determinant of neuronal outcome. Brain mitochondria isolated from 16-18-day-old rats had lower maximal, respiration-dependent Ca(2+) uptake capacity than brain mitochondria isolated from adult rats in the presence of ATP at both a pH of 7.0 and 6.5. However, in the absence of ATP, immature brain mitochondria exhibited greater Ca(2+) uptake capacity at pH 7.0 and 6.5, indicating a greater resistance of immature brain mitochondria to Ca(2+)-induced dysfunction under conditions relevant to those that exist during acute ischemic and traumatic brain injury. Acidosis reduced the maximal Ca(2+) uptake capacity in both immature and adult brain mitochondria. Cytochrome c was released from both immature and adult brain mitochondria in response to Ca(2+) exposure, but was not affected by cyclosporin A, an inhibitor of the mitochondrial membrane permeability transition. Developmental changes in mitochondrial response to Ca(2+) loads may have important implications in the pathobiology of brain injury to the developing brain.

Adenosine Triphosphate↗

PubMed2004

Mitochondrial dysfunction contributes to cell death following traumatic brain injury in adult and immature animals.

Secondary injury following traumatic brain injury (TBI) is characterized by a variety of pathophysiologic cascades. Many of these cascades can have significant detrimental effects on cerebral mitochondria. These include exposure of neurons to excitotoxic levels of excitatory neurotransmitters with intracellular calcium influx, generation of reactive oxygen species, and production of peptides that participate in apoptotic cell death. Both experimental and clinical TBI studies have documented mitochondrial dysfunction, and animal studies suggest this dysfunction begins early and may persist for days following injury. Furthermore, interventions targeting mitochondrial mechanisms have shown neuroprotection after TBI. Continued evaluation and understanding of mitochondrial mechanisms contributing to neuronal cell death and survival after TBI is indicated. In addition, important underlying factors, such as brain maturation, that influence mitochondrial function should be studied. The ability to identify, target, and manipulate mitochondrial dysfunction may lead to the development of novel therapies for the treatment of adult and pediatric TBI.

Aging↗