Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Más filtros











Base de datos
Intervalo de año de publicación
1.
J Neuroimmunol ; 394: 578427, 2024 09 15.
Artículo en Inglés | MEDLINE | ID: mdl-39116522

RESUMEN

The hypothalamus receives serotonergic projections from the raphe nucleus in a sex-specific manner. During systemic inflammation, hypothalamic levels of serotonin (5-hydroxytryptamine [5-HT]) decrease in male rats. The present study evaluated the involvement of endothelin-1 (ET-1) in the febrile response, hypolocomotion, and changes in hypothalamic 5-HT levels during systemic inflammation in male and female rats. An intraperitoneal injection of lipopolysaccharide (LPS) induced a febrile response and hypolocomotion in both male and female rats. However, although LPS reduced hypothalamic levels of 5-HT and its metabolite 5-hydroxyindol acetic acid (5-HIAA) in male rats, it increased these levels in female rats. An intracerebroventricular injection of the endothelin-B receptor antagonist BQ788 significantly reduced LPS-induced fever and hypolocomotion and changes in hypothalamic 5-HT and 5-HIAA levels in both male and female rats. The i.c.v. administration of ET-1 induced a significant fever and hypolocomotion, but reduced the hypothalamic levels of 5-HT and 5-HIAA in both males and females. These results suggest an important sexual dimorphism during systemic inflammation regarding the release of 5-HT in the hypothalamus. Moreover, ET-1 arises as an important mediator involved in the changes in hypothalamic 5-HT levels in both male and female rats.


Asunto(s)
Endotelina-1 , Hipotálamo , Inflamación , Piperidinas , Ratas Wistar , Serotonina , Caracteres Sexuales , Animales , Masculino , Femenino , Endotelina-1/metabolismo , Hipotálamo/metabolismo , Hipotálamo/efectos de los fármacos , Ratas , Inflamación/metabolismo , Inflamación/inducido químicamente , Serotonina/metabolismo , Piperidinas/farmacología , Lipopolisacáridos/toxicidad , Oligopéptidos/farmacología , Ácido Hidroxiindolacético/metabolismo , Antagonistas de los Receptores de Endotelina/farmacología , Fiebre/metabolismo , Fiebre/inducido químicamente
2.
Peptides ; 167: 171042, 2023 09.
Artículo en Inglés | MEDLINE | ID: mdl-37315714

RESUMEN

Sepsis is a serious syndrome, characterized by the excessive release of inflammatory mediators and thermoregulatory changes, being fever the most common sign. However, despite the importance of Angiotensin (Ang)-(1-7) in controlling the inflammation, the role of the peptide in the febrile response and mortality in animals submitted to experimental model of sepsis is still not clear. In this way, we evaluate the effect of continuous infusion of Ang-(1-7) in inflammatory response, thermoregulation and in mortality of Wistar male rats submitted to colonic ligation puncture (CLP). Before CLP surgery, the infusion pumps (Ang-(1-7), 1.5 mg/mL or saline) were inserted into the abdominal cavity and maintained for 24 h. CLP rats showed a febrile response starting from 3 h after and persisted until the 24th hour of experiment. Continuous treatment with Ang-(1-7) attenuated the febrile response and reestablished the euthermia 11 h after CLP, until the end of experiment, which coincided with an increased heat loss index (HLI). This effect was associated with a decrease in production of pro-inflammatory mediators in liver, white adipose tissue (WAT) and hypothalamus. Moreover, an increase in norepinephrine (NE) content in interscapular brown adipose tissue (iBAT) was observed in CLP animals, which was attenuated with treatment with Ang-(1-7), and decreased mortality in CLP animals treated with Ang-(1-7). Taken together, the present study demonstrates that continuous infusion treatment with Ang-(1-7) can promote a global anti-inflammatory effect, reestablishing the tail skin heat loss as a key thermo-effector function, resulting in an increased survival of animals submitted to experimental sepsis.


Asunto(s)
Sepsis , Cola (estructura animal) , Ratas , Masculino , Animales , Ratas Wistar , Sepsis/tratamiento farmacológico , Regulación de la Temperatura Corporal , Modelos Animales de Enfermedad
3.
Neuroimmunomodulation ; 16(1): 45-53, 2009 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-19077445

RESUMEN

OBJECTIVE: We investigated the time course of thermoregulation, nitric oxide (NO) formation and hydroelectrolytic alterations, as well as mean arterial pressure and arginine vasopressin (AVP) secretion, in experimental sepsis induced by cecal ligation and puncture (CLP). METHODS: Male Wistar rats submitted to CLP or a sham operation were divided into 4 groups, as follows: group 1, for survival rate evaluation for 24 h; group 2, for body temperature (Tb) analysis; group 3, for mean arterial pressure registration, and group 4, for blood collection and processing of the neurohypophysis and hypothalamic nuclei 0, 2, 4, 6 and 24 h after surgery. AVP levels and content were measured in plasma, neurohypophysis and the hypothalamic paraventricular and supraoptic nuclei. RESULTS: Animals which underwent CLP showed high mortality, a progressive decrease in mean arterial pressure and an increase in plasma NO. Tb dropped during the first 4 h and showed a progressive increase 6 h after surgery. Plasma AVP levels increased immediately after CLP surgery and again at 6 h, before returning to basal levels at 24 h. This was followed by a depletion of neurohypophyseal AVP content at 4 h that continued until 24 h. AVP content in the supraoptic nucleus was elevated 24 h after CLP surgery, while in the paraventricular nucleus, an increase was observed at 6 h and 24 h. CONCLUSIONS: In the present study, laparotomy and hypotension may have been responsible for the increase in plasma AVP in the initial phase of polymicrobial sepsis, and this may have contributed to the observed hypothermia. Moreover, an apparently impaired replenishment of AVP content in the neurohypophysis, possibly due to increased NO formation, may explain the impaired AVP secretion in the late phase of severe sepsis.


Asunto(s)
Arginina Vasopresina/metabolismo , Regulación de la Temperatura Corporal/fisiología , Hipotálamo/metabolismo , Sepsis/sangre , Sepsis/fisiopatología , Animales , Arginina Vasopresina/sangre , Presión Sanguínea/fisiología , Modelos Animales de Enfermedad , Progresión de la Enfermedad , Hipotensión/etiología , Hipotensión/fisiopatología , Laparotomía/efectos adversos , Masculino , Mortalidad , Óxido Nítrico/biosíntesis , Óxido Nítrico/sangre , Núcleo Hipotalámico Paraventricular/metabolismo , Ratas , Ratas Wistar , Sepsis/microbiología , Choque Séptico/sangre , Choque Séptico/microbiología , Choque Séptico/fisiopatología , Núcleo Supraóptico/metabolismo , Regulación hacia Arriba/fisiología
4.
Brain Res ; 1115(1): 83-91, 2006 Oct 18.
Artículo en Inglés | MEDLINE | ID: mdl-16934778

RESUMEN

This study examined whether electrolytic ablation of the periventricular anteroventral third ventricle (AV3V) region would affect the hypothalamic activation and the increase of hypophysial hormone secretion induced by systemic injection of lipopolysaccharide (LPS) in rats. LPS significantly increased the number of cells showing Fos immunoreactivity in the paraventricular (PVN) and supraoptic (SON) nuclei of the hypothalamus (P<0.05) and also increased plasma levels of vasopressin, oxytocin, adrenocorticotropin and corticosterone (P<0.05). AV3V lesion significantly reduced LPS-induced Fos immunoreactivity (P<0.05) and vasopressin and oxytocin secretion (P<0.05). Elevations in adrenocorticotropin but not in plasma corticosterone after LPS were affected by prior AV3V lesions. These findings demonstrate that LPS-induced Fos expression in the PVN and SON, and hypophysial hormone secretion is dependent on the integrity of the AV3V region.


Asunto(s)
Sistema Hipotálamo-Hipofisario/metabolismo , Hipotálamo/metabolismo , Hipotálamo/fisiología , Hormonas Hipofisarias/metabolismo , Tercer Ventrículo/fisiología , Hormona Adrenocorticotrópica/metabolismo , Animales , Fenómenos Fisiológicos Cardiovasculares , Modelos Animales de Enfermedad , Sistema Hipotálamo-Hipofisario/efectos de los fármacos , Hipotálamo/anatomía & histología , Hipotálamo/efectos de los fármacos , Mediadores de Inflamación/farmacología , Lipopolisacáridos/farmacología , Masculino , Neuronas/efectos de los fármacos , Neuronas/metabolismo , Oxitocina/metabolismo , Núcleo Hipotalámico Paraventricular/efectos de los fármacos , Núcleo Hipotalámico Paraventricular/metabolismo , Proteínas Proto-Oncogénicas c-fos/metabolismo , Ratas , Ratas Wistar , Choque Séptico/metabolismo , Choque Séptico/fisiopatología , Estrés Fisiológico/metabolismo , Estrés Fisiológico/fisiopatología , Núcleo Supraóptico/efectos de los fármacos , Núcleo Supraóptico/metabolismo , Tercer Ventrículo/anatomía & histología , Vasopresinas/metabolismo , Equilibrio Hidroelectrolítico/fisiología
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA