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Correspondence  |   November 2010
Isoflurane-induced Neuroapoptosis in the Neonatal Rhesus Macaque Brain: Isoflurane or Ischemia-Reperfusion?
Author Affiliations & Notes
  • Ansgar M. Brambrink, M.D., Ph.D.
    *
  • *Oregon Health & Science University, Portland, Oregon.
Article Information
Correspondence
Correspondence   |   November 2010
Isoflurane-induced Neuroapoptosis in the Neonatal Rhesus Macaque Brain: Isoflurane or Ischemia-Reperfusion?
Anesthesiology 11 2010, Vol.113, 1245-1246. doi:10.1097/ALN.0b013e3181f746b6
Anesthesiology 11 2010, Vol.113, 1245-1246. doi:10.1097/ALN.0b013e3181f746b6
In Reply:
We thank Drs. Hansen and Henneberg as well as Drs. Mazoit, Roulleau, and Baujard for expressing interest in our recent publication on neuroapoptosis in the developing nonhuman primate brain after isoflurane anesthesia.1 We appreciate the opportunity to discuss their valuable suggestions and concerns.
Before addressing Drs. Hansen and Henneberg's suggestions for the direction of future research, we would like to comment on their statement that 50–70% of all neurons die by natural apoptosis during development. As we have explained in a recent publication, this is a misconception.2 Natural apoptosis deletes a high (but unknown) percentage of neuronal (and glial) precursor  cells. However, after precursor cells differentiate into neurons and begin the synaptogenesis process, very few die by natural apoptosis, unless synaptogenesis is disrupted by some unnatural circumstance. Exposure to anesthetic drugs is an unnatural circumstance that disrupts synaptogenesis and deletes many neurons that would otherwise have survived and made a positive contribution to functions of the brain.
Drs. Hansen and Henneberg argue that further animal studies can serve no useful purpose, because there is no satisfactory way of extrapolating experimental findings from animals to humans. They express concern that more animal data will not clarify and may further confuse the issue of human susceptibility. Therefore, to move the field forward, they suggest that the research focus should now be on human research aimed at clarifying whether exposure of the developing human brain to anesthetic drugs is associated with long-term neurocognitive disturbances.
We agree that there is an urgent need for well designed human studies, but it does not logically follow that animal research is futile or should be halted. Rodent data served the very valuable purpose of alerting the medical profession and regulatory authorities to a neurotoxic action of anesthetic drugs. If it can be proven beyond reasonable doubt that anesthetic drugs, at clinically relevant doses, exert this neurotoxic action in the developing human brain, and that this results in neurodevelopmental disabilities, this would be a public health problem of considerable magnitude. Demonstrating that the nonhuman primate brain is susceptible to this neurotoxic action of anesthetic drugs when applied at clinically relevant doses does not provide definitive proof of human susceptibility, but it helps to close the translational gap and contributes new insight into the apparent species generality of this neurotoxic phenomenon.
A major benefit of the animal studies that have been performed is that they have spurred clinical researchers to conduct human studies. Several independent groups have now reported preliminary findings that tentatively support the conclusion that brief exposure of human infants to anesthesia is associated with increased risk of long-term neurobehavioral disturbances.3–7 One study did not find an association, but anesthesia exposure was documented only by parental reporting.8 These studies and the tentative nature of their conclusions illustrate the difficulty of designing and conducting definitive clinical studies of anesthetic neurotoxicity. While prospective clinical studies are designed and conducted over the next several years, further animal research can provide insights into the mechanisms of anesthetic neurotoxicity and the identification of anesthetic regimens that are not neurotoxic in neonates.
Drs. Mazoit, Roulleau, and Baujard raise an important question: is it possible that the reported findings1 may be caused by some mechanism other than a direct action of the anesthetic drug? Specifically, they postulate that hypoxia/ischemia, secondary to reduced blood pressure, can explain the neuroapoptosis response in our isoflurane-treated infant monkeys. It is important to recognize that there is no evidence for the claim that reduced blood pressure, even to an extreme degree, can trigger acute neuroapoptosis in the developing brain of any species. In contrast, there are more than 50 published reports from multiple independent laboratories showing that alcohol and anesthetic or anticonvulsant drugs do trigger acute neuroapoptosis in the developing rodent and monkey brain. Moreover, we have shown previously that hypoxia/ischemia causes an acute excitotoxic  cell death response in the developing rodent brain that is not accompanied in the acute period by any evidence of apoptotic neurodegeneration.9–11 In contrast, anesthetic drugs cause an acute apoptotic  cell death response in the developing brain that is not accompanied by any evidence of excitotoxic neurodegeneration.1,12–15 Evidence that intentional induction of profound hypoxia/ischemia does not trigger an acute apoptosis response in the developing brain signifies that it is highly unlikely that a decrease in blood pressure to a modest nonischemic degree will trigger acute neuroapoptosis.
*Oregon Health & Science University, Portland, Oregon.
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