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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Down regulation of dihydroalprenolol and imipramine binding sites in brain of rats repeatedly treated with imipramine.

In rats receiving repeated injections of imipramine, there is a reduction in the number of high affinity binding sites for [3H]imipramine and [3H]dihydroalprenolol present in crude synaptic membrane preparations from various brain structures. The location of the sites that become subsensitive to the two ligands did not coincide; the binding sites to [3H]imipramine became subsensitive in the hippocampus but not in cortex or cerebellum. In contrast the binding sites to [3H]dihydroalprenolol became subsensitive in cortex and cerebellum but not in hippocampus. It can be suggested that in rats repeatedly treated with imipramine the down regulation of beta-adrenergic receptors may not coincide with the down regulation of the high affinity binding sites for imipramine. Such a dissociation is supported further by experiments with rats treated with iprinidol.[1]

References

  1. Down regulation of dihydroalprenolol and imipramine binding sites in brain of rats repeatedly treated with imipramine. Kinnier, W.J., Chuang, D.M., Costa, E. Eur. J. Pharmacol. (1980) [Pubmed]
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