Carotid Chemoreceptor Reflex Modulation by Arginine-Vasopressin Microinjected into the Nucleus Tractus Solitarius in Rats
Autor: | Mónica Lemus, Elena Roces de Álvarez-Buylla, Alvarez-Buylla R, Alexander Yarkov, Sergio Montero |
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Rok vydání: | 2006 |
Předmět: |
Blood Glucose
Male Vasopressin Pentobarbital medicine.medical_specialty Microinjections Central nervous system Stimulation Sodium Cyanide Internal medicine Reflex Solitary Nucleus medicine Animals Homeostasis Glucose homeostasis Rats Wistar Carotid Body Chemistry General Medicine Chemoreceptor Cells Rats Arginine Vasopressin medicine.anatomical_structure Endocrinology nervous system Carotid body medicine.drug |
Zdroj: | Archives of Medical Research. 37:709-716 |
ISSN: | 0188-4409 |
DOI: | 10.1016/j.arcmed.2006.03.001 |
Popis: | Background In addition to their role of sensing O 2 , pH, CO 2 , osmolarity and temperature, carotid body receptors (CBR) were proposed by us and others to have a glucose-sensing role in the blood entering the brain, integrating information about blood glucose and O 2 levels essential for central nervous system (CNS) metabolism. The nucleus tractus solitarius (NTS) is an important relay station in central metabolic control and receives signals from peripheral glucose-sensitive hepatoportal afferences, from central glucose-responsive neurons in the brainstem and from CBR and arginine–vasopressin (AVP)-containing axons from hypothalamic nuclei. Methods In normal Wistar rats anesthetized with pentobarbital, permanent cannulas were placed stereotaxically in the NTS. Glucose changes were induced in vivo after CBR stimulation with sodium cyanide (NaCN-5 μg/100 g), preceded by an infusion of AVP [(10 or 40 pmol/100 nL of artificial cerebrospinal fluid) aCSF] or an antagonist for V1a receptors (anti-glycogenolytic vasopressin analogue-VP1-A) (100 pmol/100 nL of aCSF) into the NTS. Results CBR stimulation after an AVP infusion (larger dose) into the NTS resulted in a significantly higher arterial glucose and lower brain arterial–venous glucose difference. In the same way, VP1-A administration in the NTS significantly decreased the effects observed after AVP priming before CBR stimulation or preceding the CBR stimulation, alone. Conclusions We propose that AVP in the NTS could participate in glucose homeostasis, modulating the information arising in CBR after histotoxic-anoxia stimulation. |
Databáze: | OpenAIRE |
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