Joel S. Colton

Protection from oxidation enhances the survival of cultured mesencephalic neurons

Oxidative stress has been linked to the destruction of dopaminergic neurons in the substantia nigra and may be a significant factor in both Parkinsons disease and MPTP toxicity. Using primary cultures of embryonic rat mesencephalon and standard immunocytochemical techniques, we have examined the survival of tyrosine hydroxylase-containing (TH+) neurons cultured in the presence of antioxidants and/or in an environment of low oxygen partial pressure. The number of TH+ neurons increased approximately twofold if superoxide dismutase, glutathione peroxidase (GP), or N-acetyl cysteine (NAC) were added to the culture media. Exposure of the neurons to a 5% oxygen environment (38 torr, i.e., 38 mm Hg) also increased the survival of TH+ neurons by about twofold. A dramatic enhancement of survival, however, was seen when NAC was used in combination with the 5% oxygen environment. In this case, the number of TH+ neurons increased fourfold from nontreated controls. Morphological changes were also noted. GP increased the average neurite length while NAC increased the average area of the cell body in the TH+ neuron. These results suggest that manipulation of oxidative conditions by changing the ambient O2 tension or the level of antioxidants promotes survival of TH+ neurons in culture and may have implications for transplantation therapies in Parkinsons disease.

Changes in synaptic transmission produced by hydrogen peroxide

The effect of hydrogen peroxide (H2O2) on excitatory and inhibitory synaptic transmission was studied at the lobster neuromuscular junction. H2O2 produced a dose dependent decrease in the amplitude of the junction potential (Vejp). This decrease was due to changes in both presynaptic transmitter release and the postsynaptic response to the neurotransmitter. Observed presynaptic changes due to exposure to H2O2 were a decrease in the amount of transmitter released, that is, quantal content, as well as a decrease in the fast facilitation, that is, the amplitude increase of successive excitatory junction potentials at a rate of 3 Hz. To discern postsynaptic changes, glutamate, the putative excitatory neurotransmitter for this preparation was applied directly to the bathing medium in order to bypass the presynaptic release process. H2O2 produced a decreased response of the glutamate receptor/ionophore. The action of H2O2 was not selective to excitatory (glutamate-mediated) transmission because inhibitory (GABA-mediated) transmission was also depressed by H2O2. This effect was primarily presynaptic since H2O2 produced no change in the postsynaptic response to applied GABA.

The action of oxygen and oxygen at high pressure on inhibitory transmission

The effect of 100% oxygen at ambient pressure, 100% oxygen at 1.7 Atmospheres Absolute (ATA), 100% oxygen at 5.1 ATA, helium at 1.7 ATA and helium at 5.1 ATA on inhibitory synaptic transmission was studied using the lobster walking leg neuromuscular preparation. Exposure to 100% oxygen at ambient pressure, at 1.7 ATA or at 5.1 ATA produced a decrease in inhibitory transmission manifest as a fall in inhibitory synaptic conductance (Ginh). The largest decrease in Ginh was seen in 100% oxygen at ambient pressure, while a progressively smaller decrease was seen in 100% oxygen at 1.7 ATA and 5.1 ATA, respectively. Also associated with 100% oxygen at ambient pressure was the disappearance of inhibitory junction potentials. Pressurization with helium produced a fall in Ginh at 5.1 ATA but no change or a slight increase at 1.7 ATA. The action of either 100% oxygen at ambient and at 1.7 or 5.1 ATA or helium at 1.7 or 5.1 ATA was shown to be on presynaptic parameters since the percent decrease in Ro induced by exogenous application of gamma-aminobutyric acid (GABA), the inhibitory transmitter, was the same in either 100% oxygen at ambient pressure, 100% oxygen or helium at 1.7 ATA and 5.1 ATA. The similarity in action of oxygen to the action of isoniazid, a known glutamic acid decarboxylase (the enzyme that catalyzes the production of GABA) inhibitor in the same preparation suggests that one possible site of oxygen action is on GABA production.

Trigeminal responses to thermal stimulation of the oral cavity in rattlesnakes (Crotalus viridis) before and after bilateral anesthetization of the facial pit organs

Multiunit neural responses from the superficial maxillary branch of the trigeminal nerve in prairie rattlesnakes were elicited by intraoral thermal stimulation. The responses to oral stimulation were shown to be independent of responses obtained by thermal stimulation of the loreal pits. Histological examination of the dorsal lip, palate, and fang sheath regions revealed dense ramifying neurons in the epidermal layers of the fang sheaths that were morphologically similar to suspected infrared sensitive neurons in the pit membranes.

The action of dantrolene sodium on the lobster neuromuscular junction

Abstract 1. At a concentration of 2.3 to 3.1 × 10−5 M, dantrolene Na increased the frequency of stimulation required to elicit a visible muscle contraction from 7 stimuli/sec to a minimum of 25 stimuli/sec. 2. At the same concentration, dantrolene Na had no effect on the following pre- and post-synaptic parameters at the neuromuscular junction of the lobster: excitatory synaptic conductance, excitatory reversal potential, excitatory miniature end plate potential amplitude, excitatory quantal content per fiber, excitatory MEPP frequency, inhibitory synaptic conductance, or inhibitory reversal potential. 3. Resting input conductance was slightly, but consistently increased by dantrolene Na.