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1.
Article Dans Anglais | IMSEAR | ID: sea-159965

Résumé

Summary: Opportunistic infections are common complications of advanced immuno-deficiency in individuals with Human Immunodeficiency Virus (HIV) infection. Following involvement of the lung, the central nervous system (CNS) is the second most commonly affected organ. We report two cases of concurrent cryptococcal meningitis and tuberculosis (TB) in HIV infected persons. A high suspicion of multiple opportunistic infections should be kept in mind in HIV seropositive individuals.


Sujets)
Infections opportunistes liées au SIDA/traitement médicamenteux , Infections opportunistes liées au SIDA/microbiologie , Infections opportunistes liées au SIDA/physiopathologie , Adulte , Antirétroviraux/administration et posologie , Antifongiques/administration et posologie , Antituberculeux/administration et posologie , Co-infection , Cryptococcus neoformans/isolement et purification , Infections à VIH/complications , Infections à VIH/traitement médicamenteux , Humains , Mâle , Méningite cryptococcique/complications , Méningite cryptococcique/traitement médicamenteux , Méningite cryptococcique/physiopathologie , Résultat thérapeutique , Tuberculose pulmonaire/traitement médicamenteux , Tuberculose pulmonaire/imagerie diagnostique
2.
Indian J Physiol Pharmacol ; 1995 Oct; 39(4): 369-76
Article Dans Anglais | IMSEAR | ID: sea-106216

Résumé

Chemitrodes which permit electrical and chemical stimulation of the same hypothalamic loci were implanted in anterior hypothalamic and preoptic regions. These sites were stimulated electrically using biphasic square wave pulse (1 ms, 60 Hz) at a current strength ranging from 150-800 microA to evoke an aggressive response. At lower current strength of 150-200 micro A, defence response, a sort of non-specific response can be elicited from these regions. Increasing the current strength to 400 microA led to the recruitment of affective and somatic components and changed the response pattern either to affective attack or flight. The loci producing affective attack response were localized more laterally and ventrally while the loci producing flight response were located in the dorsomedial regions of the hypothalamus. In this response the animal made a goal-directed attempt to escape through an escape route. Increasing the current strength to 500 microA in the dorsomedial regions changed the flight response to violent flight, which involved vigorous running with unsheathed claws and attacking objects if obstructed. Similar increase in current strength at loci producing affective attack only led to a decrease in the latency of response and made the attack more vigorous. Microinfusion of carbachol in graded doses of 2-15 microgram at all these loci produced a profound affective display. At lower doses of 2 and 5 microgram, only some components of affective display like alertness, pupillary dilation and ear flatness were exhibited. Increasing the dose to 10 micrograms and 15 micrograms led to the recruitment of other affective components like piloerection, salivation, hissing and baring of teeth. Microinfusion of carbachol at all loci producing affective attack on electrical stimulation produced a prononced affective display while microinfusion of carbachol at loci producing flight response led to the development of defence posture. At six loci a typical flight response was obtained while violent flight was never exhibited at any of these sites. Microinfusion of atropine (10 microgram in 1.0 microliter saline) at these loci completely blocked the carbachol induced response. Both somatomotor and affective components were completely inhibited. However, the responses obtained on electrical stimulation were not totally blocked following atropine infusion and some of the somatomotor and affective components could be elicited with higher current strength. These studies indicate the involvement of cholinoceptive mechanisms in the elicitation of hypothalamically induced aggresive behaviour. Microinfustion of hexamethonium bromide, a nicotinic blocker in 50 micrograms doses did not affect the aggressive response.


Sujets)
Agressivité/effets des médicaments et des substances chimiques , Animaux , Atropine/administration et posologie , Carbachol/administration et posologie , Chats , Stimulation électrique , Électrodes implantées , Femelle , Hexaméthonium/administration et posologie , Hypothalamus/anatomie et histologie , Hypothalamus antérieur/effets des médicaments et des substances chimiques , Mâle , Microinjections , Agonistes muscariniques/administration et posologie , Antagonistes muscariniques/administration et posologie , Antagonistes nicotiniques/administration et posologie , Aire préoptique/effets des médicaments et des substances chimiques , Activation chimique
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