Traumatic brain injury (TBI) results from a blow to the head and can range in severity from mild (e.g., brief change in mental status or consciousness) to severe (e.g., extended unconsciousness, prolonged amnesia, altered cognitive function). Trauma to the brain is the most likely type of injury to cause death or permanent disability. The costs of TBI to our society are enormous when measured by any criterion. In the general population, the risk of TBI is fairly constant throughout the lifespan, but military personnel are at much higher risk. In fact, TBI has been coined the signature injury suffered by soldiers and marines serving in Afghanistan and Iraq and accounts for about 30% of all combat casualties. It has been estimated that 10-20% of veterans of the current conflicts (150,000-300,000) have TBI of some kind. TBI is most accurately classified as a polytrauma in light of the fact that multiple organ systems can be altered. What is more, the effects of even mild TBI are cumulative and can increase the risk of co-morbid illnesses involving the central nervous system such as PTSD and Parkinson's disease. Substance abuse and alcohol abuse in particular, is a major complicating factor in TBI and should also be considered as a co-occurring condition in its own right. Alcohol abuse is steadily increasing among active military personnel and has long been a serious affliction among veterans. Like TBI, alcohol abuse can cause damage to the CNS but very little is known about how alcohol influences the severity and outcome of TBI. Recognizing that alcohol abuse and TBI are bi-directionally related for risk and consequences, the goal of research in this application is to achieve a better understanding of how these two conditions interact to determine long-term outcomes. To achieve this goal, Specific Aim 1 will analyze how binge alcohol intake prior to TBI alters the major signs and symptoms of brain injury to include edema, hypoperfusion, increased inflammation, neuronal damage, and diminished cognitive ability.
Specific Aim 2 will evaluate these same outcome measures when binge alcohol treatment follows TBI.
Specific Aim 3 will determine if TBI subsequently increases voluntary intake of alcohol. We will use validated mouse models of closed head injury and binge alcohol intoxication to pursue the goals of this application.
Traumatic brain injury (TBI) is a serious public and military health problem. The severe cost of TBI to our society is seen in many forms and includes long-term disability, the challenging courses taken by prolonged rehabilitation, and the expense associated with treatment and recovery. Alcohol abuse is also a serious public health care concern. TBI and alcohol abuse are co-occurring conditions and each can increase the risks and problems associated with the other. Active military personnel and veterans are at higher risk for both conditions by comparison to civilians and it only seems logical to suggest that alcohol abuse would worsen TBI and vice versa. However, the results from clinical and basic studies to date on alcohol-TBI interactions are surprisingly paradoxical in that some report that alcohol worsens TBI, others report that alcohol lessens the effects of TBI, and still others report that alcohol dos not alter TBI. In view of the prevalence of alcohol abuse in TBI, and considering how little is known about how these conditions interact to determine long-term outcomes, it is imperative that we achieve a better understanding of the nature of their interactions.
| Acabchuk, Rebecca; Briggs, Denise I; Angoa-Pérez, Mariana et al. (2016) Repeated mild traumatic brain injury causes focal response in lateral septum and hippocampus. Concussion 1: |
| Briggs, Denise I; Angoa-Pérez, Mariana; Kuhn, Donald M (2016) Prolonged Repetitive Head Trauma Induces a Singular Chronic Traumatic Encephalopathy-Like Pathology in White Matter Despite Transient Behavioral Abnormalities. Am J Pathol 186:2869-2886 |
| Angoa-Pérez, Mariana; Kane, Michael J; Briggs, Denise I et al. (2014) Animal models of sports-related head injury: bridging the gap between pre-clinical research and clinical reality. J Neurochem 129:916-31 |
| Kuhn, Donald M; Angoa-Pérez, Mariana; Thomas, David M (2011) Nucleus accumbens invulnerability to methamphetamine neurotoxicity. ILAR J 52:352-65 |
