Location of Propofol-Binding In order to determine the location of propofol binding, researchers conducted mutational analysis. The figure below illustrates the importance of the amino acids from 354 to 388 in presence of propofol. It is evident that deletion of these amino acids results in a lower potentiation of current by the GABA A receptors. Because of this, the GABA A receptor protein is less responsive to propofol, resulting in a more responsive neuron and thus reducing the effects of propofol as an anesthetic. In the potentiation curves (B in the figure below), the chloride ion current is measured under different conditions. In the wild type, the addition of propofol increased the chloride ion current. However, when amino acids 354-388 are deleted, the current is only slightly changed, indicating the significance of these amino acids. If the GABA A receptor is mutated, the protein is less responsive to propofol, resulting in a more responsive neuron and thus mitigating the effects of propofol as an anesthetic. Synaptic Cleft The space between two neurons is the synaptic cleft. The GABA A receptor is a transmembrane receptor protein activated by the inhibitory neurotransmitter gamma-aminobutyric acid (GABA). Under normal conditions, GABA is released from one neuron and is received by the GABA A receptor protein found in the membrane of the other neuron, inhibiting its activity. In the presence of propofol the GABA A receptor is more easily activated by GABA, resulting in the termination of the signal. GABA A Receptor: Knocked Out Whitefish Bay SMART Team: Jack Middleton, WentongZhang, Shawn Wang, Na’ilScoggins, Frank Zhang, John Park, John Schroeder, Sam Broadnax, Jieun Heo and Morgan Phillips Teachers: Paula Krukar, Marisa Roberts, Lisa Krueger and Katie Brown Mentor: Robert Peoples, Ph.D., Department of Biomedical Sciences, Marquette University The SMART Team Program (Students Modeling A Research Topic) is funded by a grant from NIH-SEPA 1R25OD010505-01 from NIH-CTSA UL1RR031973. The Nervous System The brain is the command center of the human body. Signals from all over the body are ultimately received in the brain. Anesthetics drastically reduce signaling in the brain. This results in a loss of responsiveness and unconsciousness. Thus, anesthetics are administered prior to surgery to induce a state of unconsciousness. The drugs increase inhibition in the brain, resulting in the non-transfer of excitatory electrochemical signals. Therefore, the patient is rendered unconscious and pain is not felt, which allows major surgery to be performed. Significance of Propofol Propofol is one of the most commonly used anesthetics in modern medicine. Propofol interacts with the GABA A receptor protein resulting in the termination of a signal. When enough signals are inhibited, brain function slows to the point that the body enters a state of unresponsiveness, leading to unconsciousness. Too much inhibition causes the nervous system to shut down, resulting in coma or even death. Each year in the United States, misuse of anesthetics results in 34 deaths and is a contributing factor for another 281. By understanding the interaction between GABA A protein receptors and propofol, researchers can synthesize new compounds to serve as better anesthetics in hopes of reducing the number of complications of anesthetics. Abstract Today, surgeons and dentists would not consider operating without the use of anesthetics, drugs that help numb pain and induce unconsciousness by inhibiting the transmission of signals in nerve cells. The GABA A receptor is a transmembrane receptor protein activated by the neurotransmitter gamma-aminobutyric acid (GABA) that plays a crucial role in the action of proprofol as an anesthetic. The Whitefish Bay SMART (Students Modeling A Research Topic) Team is modeling the GABA A receptor protein using 3D printing technology. When activated, the GABA A receptor selectively allows chloride ions to pass through the membrane and into the cell, creating a more negative overall charge inside the cell. When a nerve cell is excited, a sudden change in ion concentrations triggers an electrochemical potential across the cell membrane, ultimately resulting in the passage of the original signal to the next neuron. However, the GABA A receptor acts as an inhibitor, and impedes the spreading of the message by making the cell less likely to be in an excited state, causing the cell to relay a neural signal less frequently. Propofol produces its effects by enhancing the activity of the GABA A receptor. Currently, researchers are trying to pinpoint how propofol acts on the GABA A receptor protein because its molecular mechanism is not fully understood. It has been found that a phenylalanine at position 385 on the GABA A receptor is necessary for propofol to produce its effects. Research targeting how propofol alters the function of the GABA A receptor may lead to the development of more effectiveanesthetics with fewer side effects. Normal With Propofol When the GABA A receptor is activated, it allows negatively charged chloride ions to pass through its channel, making the membrane voltage more negative and the neuron less likely to fire. This inhibition may block the transmission of the signal from the nerve cell. However, the signals may still pass and the cell may still transfer the message. Propofol is an allosteric modulator, which means that it effectively enhances the effects of the GABA A receptor protein without binding to the GABA site. The chloride ions flow into the neuron, making the membrane voltage highly negative, which results in the termination of the original signal. Conclusion While significant advances have been made in understanding the function of the GABA A receptor protein, there is still more to learn about the active sites of the protein. Currently, scientists understand the general function of propofol - the anesthetic enhances the GABA A ’s function of inhibiting neural signals from traveling, which in turn results in normal human alertness to be replaced with sedation or loss of consciousness. However, it is unclear exactly how propofol affects the GABA A receptor, and research may be able to aid in uncovering this mystery. Potential benefits of this research would be that anesthetics would be safer and more effective. Although the understanding of the effect of propofol has come a long way, more milestones must be reached in order to ensure a safer and more effective use of this and other anesthetics. Works Cited Moraga-Cid, Gustavo, Gonzalo, E., Yevenes, Gunther, Schmalzing, Robert, W., Peoples, Luis, G., Aguayo. "A Single Phenylalanine Residue in the Main Intracellular Loop of α1 γ-aminobutyricAcid Type A and Glycine Receptors Influences Their Sensitivity to Propofol." (2011) Fischer, Andreas. "Under the Knife: Study Shows Rising Death Rates from General Anesthesia." Time. Time, 4 Aug. 2011. Web. 25 Feb. 2013. Structure of Propofol Signal is propagated Neuron A fires, sending an excitatory signal A B C GABA A receptor GABA GABA-releasing neuron Neuron A fires, sending an excitatory signal A B C GABA A receptor GABA GABA-releasing neuron Signal is stopped Propofol indianapublicmedia.org