Stevens C F, Wang Y
Howard Hughes Medical Institute, Salk Institute, La Jolla, California 92037.
Nature. 1993 Jul 8;364(6433):147-9. doi: 10.1038/364147a0.
Evidence that carbon monoxide can serve as an intercellular messenger in brain, a role much like that demonstrated for nitric oxide in various tissue, prompted us to investigate whether carbon monoxide participates in long-term potentiation (LTP), the cellular mechanism that may underlie certain forms of learning and memory. Although LTP is triggered in the postsynaptic neuron, at least some fraction of LTP is expressed presynaptically as an increase in the quantity of neurotransmitter released. Thus, a retrograde signal must form the communication link between the postsynaptic site of induction and the presynaptic site of expression. To test whether carbon monoxide might act as a retrograde signal in LTP, we have investigated the effect on LTP of inhibitors of the enzyme haem oxygenase-2, which catalyses the production of carbon monoxide in the brain. We find that these inhibitors prevent the induction of LTP and have no effect on one form of long-term depression. Furthermore, they will reverse LTP that is already established.
有证据表明一氧化碳可作为大脑中的一种细胞间信使,其作用很像各种组织中已被证实的一氧化氮的作用,这促使我们去研究一氧化碳是否参与长时程增强(LTP),即可能是某些学习和记忆形式基础的细胞机制。尽管LTP是在突触后神经元中触发的,但至少部分LTP是在突触前表现为释放的神经递质数量增加。因此,逆行信号必须在诱导的突触后位点和表达的突触前位点之间形成通信联系。为了测试一氧化碳是否可能在LTP中充当逆行信号,我们研究了催化大脑中一氧化碳生成的血红素加氧酶-2抑制剂对LTP的影响。我们发现这些抑制剂可阻止LTP的诱导,并且对一种形式的长时程抑制没有影响。此外,它们会逆转已经建立的LTP。