I thank Drs. Sedensky and Morgan for highlighting an area of genetic research on general anesthetics that, because of space limitations, was not included in my editorial.1
Their research dating back to 19872
has used unbiased forward genetic screens in a nematode, Caenorhabditis elegans
, identifying genes that influence sensitivity to volatile anesthetics in tests of motor function. Others have similarly exploited the fruit fly, Drosophila melongaster
. This research has contributed to our understanding of anesthetic mechanisms and bolsters my view that volatile drugs probably act via
a wide variety of targets, which may include ion channels, neurotransmitter release mechanisms, mitochondria, and others not yet discovered.
One area where my thinking diverges from that of Sedensky and Morgan relates to the role of mitochondrial complex I as a putative anesthetic target. Logically, unless confounding effects perturb the pertinent phenotype, knockout of an important primary anesthetic target gene should reduce anesthetic sensitivity
in the transgenic organism. However, knockout of Ndufs4 in mitochondrial complex I in mice results in a dramatic gain of sensitivity
to volatile anesthetics,3
undermining the idea that volatile anesthesia depends on the presence of this protein in normal animals. Clearly, other targets are mediating general anesthesia in the knockout animals. As noted by the authors,3
there are myriad mechanistic explanations for this phenotype, including that inhibition of complex I contributes to anesthesia. Thus, inferences regarding a role of mitochondrial complex I in general anesthesia are quite weak and require more rigorous experimental assessment. Nonetheless, the Ndufs4 knockout animal is a useful model for patients with mitochondrial diseases, who are also remarkably sensitive to volatile anesthetics.4
Volatile anesthetics are a mainstay of clinical practice, and understanding the mechanisms of their therapeutic actions and toxicities is a worthy scientific goal with potential implications for future drug development. As noted by Sedensky and Morgan, volatile anesthesia is a “difficult problem.” Its solution will require sophisticated research models and approaches, as well as thoughtful data analysis.
Stuart A. Forman, M.D., Ph.D.
, Massachusetts General Hospital, Boston, Massachusetts. email@example.com
1. Forman SA. The expanding genetic toolkit for exploring mechanisms of general anesthesia. Anesthesiology. 2013;118:769–71
2. Sedensky MM, Meneely PM. Genetic analysis of halothane sensitivity in Caenorhabditis elegans. Science. 1987;236:952–4
3. Quintana A, Morgan PG, Kruse SE, Palmiter RD, Sedensky MM. Altered anesthetic sensitivity of mice lacking Ndufs4, a subunit of mitochondrial complex I. PLoS One. 2012;7:e42904
4. Morgan PG, Hoppel CL, Sedensky MM. Mitochondrial defects and anesthetic sensitivity. Anesthesiology. 2002;96:1268–70
© 2013 American Society of Anesthesiologists, Inc.