Iron, a major oxidant in vivo, could be involved in atherosclerosis through the induction of the formation of oxidized LDL, a major atherogenic factor. This study was designed to test this hypothesis experimentally. Four groups of New Zealand White rabbits were included: iron-overloaded/hypercholesterolemic (group A, n = 8), iron-overloaded (group B, n = 6), hypercholesterolemic (group C, n = 6), and untreated (group D, n = 6). Iron overload was achieved by the intramuscular administration of 1.5 g of iron dextran divided in 30 doses. Hypercholesterolemia was produced by feeding rabbit chow enriched with 0.5% (wt/wt) cholesterol. Serum iron, ferritin, cholesterol, triglycerides, and lipoperoxides in serum were measured throughout the study. Lipoperoxides were measured at the end of the study in liver, aorta, and spleen homogenates. Aortas of groups A and C had multiple lesions; however, group A had greater lesional involvement than group C (P < .05). Lesions were not observed in rabbits fed normal chow (group D). As expected, serum iron and ferritin were above normal levels in groups A and B. Serum cholesterol increased in groups A and C. Lipoperoxides in liver and spleen homogenates of iron-overloaded rabbits were increased. Interestingly, iron deposits were seen by ultrastructural studies in the arterial walls of rabbits in groups A and B. Our study suggests that iron overload augments the formation of atherosclerotic lesions in hypercholesterolemic rabbits.
Six different types of spectral responses were recorded from horizontal cells under mesopic conditions in perfused retina, isolated from the dark-adapted mojarra (Eugerres plumieri). They were tentatively termed photopic Lr-, Lg1-, Lg2-, Lb-, and C-type, and scotopic L-type. The Lr-, Lg-, and Lb-type responses showed a maximum peak at 605, 550, and 516 nm respectively, while the C-type was composed of hyperpolarizing potentials in response to shorter wavelengths and depolarizing potentials in response to longer wavelengths (so-called R/G-type). The scotopic L-type has a peak at 516 nm in the spectral response and a slow decay phase in the waveform response. Following a brief period of diffuse illumination, it was found that the Lg1-type response is altered to the Lr-type, while both Lg2- and Lb-type responses change to the C-type. Intracellular marking with Lucifer or Procion yellow identified the cellular origins of different response types: external (He) and medial horizontal (Hm) cells for the Lr-type, internal horizontal (Hi) cells for the C-type, and rod-horizontal (Hr) cells for the scotopic L-type. Only He cells were found to possess an axon, while dye coupling was seen between axonless Hm, Hi, or Hr cells but not between He cells. The morphology of these fluorescent dye-marked cells was the same as that of the respective cells observed in Golgi-stained materials.
The histochemical method of Häusler was employed to demonstrate carbonic anhydrase (CA, carbonate hydrolase, 4.2.1.1.) in tissue sections. The CA reaction was inhibited in the presence of 5 mM acetazolamide. In the frog and fish retinas the CA activity was positive in the Müller fiber, the laminated segment of the cones and the myelin of the axons, and was negative in the laminated segment of the rods, the photoreceptor ellipsoid and myoid, the horizontal, bipolar, amacrine and ganglion cells, and the pigment epithelium. In the spinal cord of cat and fish the CA activity was positive in the myelin of the axons, the perineuronal oligodendroglia and the protoplasmic astrocytes, and was negative in the cell body, dendrite, and axon of the neurons and in the fibrous astrocytes. In the dorsal root ganglion of the cat CA reaction was positive in the satellite cells and the myelin, and was negative in the neuronal cell body and its processes. The capillaries in central nervous tissue show no CA reaction. The erythrocyte is CA positive while the mitochondria are CA negative.
Contacts between horizontal and bipolar cells are described in the retina of the teleost Eugerres plumieri. A single, long expansion observed in the external cone horizontal cells makes contact by means of a terminal button with the cell body of a bipolar. It represents the only contact between this class of horizontal cell and the bipolar soma. On the other hand, the medial and internal cone horizontal cells and the rod horizontal cells, which lack such a single, long expansion, display instead numerous short and fine expansions that terminate by means of a terminal knob on a bipolar cell body. The bipolar-destined, short expansions of the rod horizontal cell make contact with large bipolar cell bodies, whereas corresponding short expansions of cone horizontal cells contact small bipolar cell bodies. It is suggested that the ascending horizontal cell process forms presynaptic terminals in the photoreceptor triad complex, and that the single, long and the multiple, short bipolar-destined expansions are postsynaptic to the bipolar cell body.
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