Cordes interaction effects

Hammett plots have been constructed for the acid- and base-catalysed decomposition of methyl hemiacetals of benzaldehydes in aqueous solution. The data are analysed in terms of three-dimensional More O Ferrall-Jencks diagrams and of Cordes interaction effects. 

Sullivan AP, Dashwood MR, Dickenson AH (1987) ai adrenoceptor modulation of nociception in rat spinal cord location, effects and interaction with morphine. Eur J Pharmacol 138 169-177... 

Cordes et al995 carried out alkaline hydrolyses of p-nitrophenylhexanoate 55 (PNPH) in the presence of poly-4-vinylpyridine partially quaternized with dodecyl-bromide and ethylbromide (QPVP). They also found that the polyelectrolytes are increasingly effective as catalysts with an increasing ratio of dodecyl to ethyl groups, and the hydrophobic interactions are important in determining the catalytic efficiency. They observed the inhibitory effects of several gegen-anions fluoride ions are the weakest inhibitor, and nitrate is the strongest (F- < Cl < S04 [Pg.159]

In addition to changes within the nerve, sympathetic afferents become able to activate sensory afferents via as yet poorly characterised a-adrenoceptors. These interactions between adjacent sensory and autonomic nerve axons and between ganglion cells result in excitation spreading between different nerve fibres. These peripheral ectopic impulses can cause spontaneous pain and prime the spinal cord to exhibit enhanced evoked responses to stimuli, which themselves have greater effects due to increased sensitivity of the peripheral nerves. 

The first identified Ascaris FaRP, AF1 (KNEFIRFamide), and the structurally related peptide, AF2 (KHEYLRFamide), have been found to inhibit locomotory waves when injected into adult worms (Cowden et al., 1989 Cowden and Stretton, 1993). Their effects on body-wall muscle strips are biphasic, comprising a transient relaxation followed by an extended period of increased contractile activity (Maule et al., 1995b Bowman et al., 1996). When using muscle strips that have had the motor nerve cords removed, only the inhibitory actions of AF1 and AF2 are seen (Maule et al., 1995b). This suggests that the inhibitory phase is due to post-synaptic effects on body-wall muscle in the worm. In contrast, the excitatory effects are nerve-cord dependent and are not observed in muscle strips that have been denervated. Another possibility is that the peptides interact with receptors at the post-synaptic junction - these are also removed in specimens that have had the motor nerve cords removed. 

Zolpidem (1) is an effective hypnotic agent indicated for the short-term treatment of insomnia. Zolpidem interacts with the GABAa receptor, and its pharmacological effect is blocked by the benzodiazepine-receptor antagonist fiumazenil (Sanger and Depoortere, 1998). Zolpidem displaces benzodiazepines more selectively from the cerebellum than the hippocampus or spinal cord, consistent with preferential interaction with the ajGABAA receptor subtype (sometimes referred to as the benzodiazepine coi receptor). Studies... 

It is a potent opioid analgesic. Chemically it is N-phenyl-N-propanamide. It interacts predominantly with opioid p-recep-tor in human brain, spinal cord and other tissues. It exerts its principle pharmacologic effects on the CNS. It is 80-100 times more potent than morphine, both in analgesia and respiratory depression. 

This syndrome most often occurs as a result of the interaction of two or more drugs acting via different mechanisms to potentiate the central effects of serotonin at 5-HTi receptors in the brainstem and spinal cord (490). It consists of the following symptoms ... 

Tramadol has about one tenth the pain-relieving ability of morphine.53 There are two enantiomers, and both contribute to pain relief, but via different mechanisms. (+)-Tramadol and the metabolite (+)-0-desmethy 1-tramadol, which is referred to as Ml, are agonists of the mu opioid receptor. (+)-Tramadol inhibits serotonin reuptake and (-)-tramadol inhibits norepinephrine re uptake.25 This latter action enhances the inhibitory effects on pain transmission in the spinal cord. Because the actions of the two enantiomers are complementary, they are usually supplied as a racemic mixture. However, because it is a serotonin-reuptake blocker, interaction with other medications can lead to the occurrence of serotonin syndrome.54... 

Opioids basically exert their analgesic effects by inhibiting synaptic transmission in key pain pathways in the spinal cord and brain. This inhibitory effect is mediated by opioid receptors that are located on both presynaptic and postsynaptic membranes of pain-mediating synapses (Fig. 14—2). In the spinal cord, for example, receptors are located on the presynaptic terminals of primary (first-order) nociceptive afferents, and when bound by opioids, they directly decrease the release of pain-mediating transmitters such as substance P.35,38 Opioid drug-receptor interactions also take place on the postsynaptic membrane of the secondary afferent neuron—that is, the second-order nociceptive afferent neuron in the spinal cord.19,33 When stimulated, these receptors also inhibit pain transmission by hyperpolarizing the postsynaptic neuron.19... 

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