Tesis
Participação da área septal medial nas respostas sialogoga, dipsogênica e cardiovascular induzidas pela pilocarpina
Fecha
2008-04-30Registro en:
PAULIN, Renata Fabris. Participação da área septal medial nas respostas
sialogoga, dipsogênica e cardiovascular induzidas pela
pilocarpina. 2008. 106 f. Dissertação (Mestrado em Ciências Biológicas) - Universidade Federal de São Carlos, São Carlos, 2008.
Autor
Paulin, Renata Fabris
Institución
Resumen
Peripheral injection of pilocarpine (PILO, 1 mg/Kg of body weight),
muscarinic cholinergic agonist, induce salivation, water intake and pressor response.
The medial septal area (MSA) is an important brain area involved in cardiovascular
regulation and hydroelectrolytic control. In this present study, we investigated: 1) the
effect of MSA electrolytic lesion or the blockade of muscarinic cholinergic receptors
into MSA on salivation, water intake and cardiovascular responses induced by
peripheral pilocarpine; 2) the role of the sympathetic nervous system and/or
vasopressin on the cardiovascular responses induced by peripheral pilocarpine; 3) the
effect of injection of pilocarpine into MSA on salivation, water intake and
cardiovascular responses. Male Holtzman rats weighing 280 to 320 g were submitted
to 1 or 15 days MSA electrolytic lesion (2 mA x 5 s) or stainless steel guide cannulas
were stereotaxically implanted into the MSA. We observed that peripheral
pilocarpine (1 mg/kg of body weight) induces salivary secretion, water intake and an
increase in mean arterial pressure (MAP) . This increase in MAP is due to an
activation of simpathetic nervous system, since it was significantly reduced by
previous treatment with prazosin (1 mg/kg of body weight), but not by vasopressin
V1a receptor antagonist (10 µg/kg of body weigh). The salivary secretion and
dipsogenic response induced by peripheral pilocarpine was reduced by MSA
eletrolytic lesion or MSA muscarinic cholinergic blockade. Nonetheless, the pressor
response induced by peripheral pilocarpine was not depend of MSA, since MSA
eletrolytic lesion or muscarinic cholinergic receptors blockade did not change this
response. Pilocarpine injection into MSA induced water intake (200 e 500 nmol/0,5
µL), salivary secretion (500 nmol/0,5 µL) and MAP increase (500 nmol/0,5 µL). Our
results show that peripheral or MSA injection of pilocarpine induce salivary
secretion, water intake and pressor response. The pressor response induced by
peripheral pilocarpine is due to sympathetic activation. The MSA and its muscarinic
cholinergic receptors are involved in the salivary secretion and water intake, but not
in the control of pressor response induced by peripheral pilocarpine, suggesting that
MSA has a differencial control on the responses induced by peripheral pilocarpine.