Why the study?
Does haemoglobin inhibit cGMP accumulation induced by glutamate receptor agonists in adult rat cerebellar slices?
Does haemoglobin inhibit cGMP accumulation induced by glutamate receptor agonists in adult rat cerebellar slices?
Nitric oxide functions predominantly as an intercellular messenger in intact brain tissue, as its effects are inhibited by extracellular haemoglobin.
Hb blocks NO effects in rat slices; leaves open whether this intercellular messenger role applies in human brain.
Nitric oxide (NO) is a novel messenger molecule that is produced following glutamate receptor activation and which stimulates cyclic GMP (cGMP) formation. To determine if the mode of action of NO is predominantly intra- or inter-cellular in intact brain tissue, we tested the ability of haemoglobin (Hb), a NO-binding protein that remains extracellular, to inhibit cGMP accumulation induced by glutamate receptor agonists in adult rat cerebellar slices. Responses to agonists acting selectively on N-methyl-D-aspartate (NMDA) and non-NMDA glutamate receptors were inhibited by Hb (IC50 approximately 20 microM) suggesting that NO functions predominantly as a mediator of communication between cells. The effects of NO-donating drugs (e.g. nitroprusside) were also inhibited by Hb, implying that they yield NO extracellularly.
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Southam et al. (1991) studied this question.
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