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1.
Neuroscience ; 61(2): 411-20, 1994 Jul.
Article in English | MEDLINE | ID: mdl-7526268

ABSTRACT

The amphibian Xenopus laevis is able to adapt the colour of its skin to the light intensity of the background, by releasing alpha-melanophore-stimulating hormone from the pars intermedia of the hypophysis. In this control various inhibitory (dopamine, gamma-aminobutyric acid, neuropeptide Y, noradrenaline) and stimulatory (thyrotropin-releasing hormone and corticotropin-releasing hormone) neural factors are involved. Dopamine, gamma-aminobutyric acid and neuropeptide Y are present in suprachiasmatic neurons and co-exist in synaptic contacts on the melanotrope cells in the pars intermedia, whereas noradrenaline occurs in the locus coeruleus and noradrenaline-containing fibres innervate the pars intermedia. Thyrotropin-releasing hormone and corticotropin-releasing hormone occur in axon terminals in the pars nervosa. In the present study, the neuronal origins of these factors have been identified using axonal tract tracing. Application of the tracers 1,1'dioctadecyl-3,3,3',3' tetramethyl indocarbocyanine and horseradish peroxidase into the pars intermedia resulted in labelled neurons in two brain areas, which were immunocytochemically identified as the suprachiasmatic nucleus and the locus coeruleus, indicating that these areas are involved in neural inhibition of the melanotrope cells. Thyrotropin-releasing hormone and corticotropin-releasing hormone were demonstrated immunocytochemically in the magnocellular nucleus. This area appeared to be labelled upon tracer application into the pars nervosa. This finding is in line with the idea that corticotropin-releasing hormone and thyrotropin-releasing hormone stimulate melanotrope cell activity after diffusion from the neural lobe to the pars intermedia. After anterograde filling of the optic nerve with horseradish peroxidase, labelled axons were traced up to the suprachiasmatic area where they showed to be in contact with suprachiasmatic neurons. These neurons showed a positive reaction with anti-neuropeptide Y and the same held for staining with anti-tyrosine hydroxylase. It is suggested that a retino-suprachiasmatic pathway is involved in the control of the melanotrope cells during the process of background adaptation.


Subject(s)
Hypothalamo-Hypophyseal System/physiology , Locus Coeruleus/physiology , Pituitary Gland, Anterior/metabolism , Preoptic Area/physiology , Retina/physiology , Skin Pigmentation/physiology , Suprachiasmatic Nucleus/physiology , Xenopus laevis/physiology , alpha-MSH/metabolism , Adaptation, Physiological/physiology , Afferent Pathways/physiology , Afferent Pathways/ultrastructure , Animals , Axonal Transport , Brain Mapping , Carbocyanines , Corticotropin-Releasing Hormone/physiology , Horseradish Peroxidase , Locus Coeruleus/cytology , Melanophores/physiology , Neurotransmitter Agents/metabolism , Optic Nerve/physiology , Pituitary Gland, Anterior/cytology , Preoptic Area/cytology , Skin Pigmentation/radiation effects , Suprachiasmatic Nucleus/cytology , Thyrotropin-Releasing Hormone/physiology
2.
Acta Trop ; 50(3): 227-36, 1992 Feb.
Article in English | MEDLINE | ID: mdl-1348599

ABSTRACT

The full development of Plasmodium falciparum in Anopheles stephensi mosquitoes was studied by scanning electron microscopy. Ookinetic development was described from in vitro cultures. Growing oocysts beneath the basal lamina of the midgut wall mechanically stretch this lamina until it is torn and displaced by day 7. In young oocysts the wall appears smooth. In older oocysts wrinkles in the wall are visible after routine fixation. Osmium tetroxide postfixation greatly reduced the occurrence of these wrinkles. Intracapsular development of sporozoites was visualized after mechanical manipulation of the oocysts during sample preparation. In contrast to P. berghei, no ectopic development was seen in P. falciparum in the mosquito midgut. The mechanism of sporozoite escape from the oocyst appears to be similar to that described for rodent malaria. Fracturing of salivary glands provided the first view by scanning electron microscopy of sporozoites located in proximal and distal gland cells and in the draining duct.


Subject(s)
Anopheles/parasitology , Insect Vectors/parasitology , Plasmodium falciparum/growth & development , Animals , Anopheles/ultrastructure , Insect Vectors/ultrastructure , Microscopy, Electron, Scanning , Plasmodium falciparum/ultrastructure
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