Neural regulation of water balance is mediated by a circuit that includes circumventricular and forebrain structures. These structures respond to plasma and cerebrospinal fluid hyperosmolality, angiotensin II and input from volume- and baroreceptors. Experiments outlined in this proposal will continue studies that we began five years ago. We will test the hypothesis that the metabolic activity of the subfornical organ, a circumventricular organ, is modified by sensory and humoral inputs and by several neurotransmitters. To test this hypothesis three groups of experiments were designed: (1) we will investigate whether the inputs from baroreceptors alter the functional activity of the subfornical organ in response to peripheral angiotensin II; (2) we will investigate whether the subfornical organ is the primary site of action of angiotensin II; and (3) we will investigate whether the subfornical organ is responsive to different neurotransmitters and whether multiple circuits are activated by them. The primary methodology will involve the autoradiographic (14C) deoxyglucose technique. The first question will be investigated in sino-aortic denervated and sham-operated preparations. The primary site of action of AII will be investigated in preparations in which connections between the subfornical organ and the anteroventral third ventricle (AV3V) area are interruped. Some investigators have indicated that the primary site of AII activation may be the AV3V area. If angiotensin II increases glucose utilization in the subfornical organ of lesioned rats to the same degree as in sham-operated animals, this will indicate that angiotensin II stimulation of the subfornical organ is not dependent on input from AV3V area. Multiplicity of circuits within the subfornical organ subserving drinking behavior will be examined by topically stimulating the subfornical organ with putative neurotransmitters angiotensin II, serotonin, and acetylcholine. Comparison of the patterns of activation of neural structures and behavior by each of these pharmacologic agents will allow us to determine whether there are multiple circuits in the subfornical organ.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
1R01NS023055-01A1
Application #
3406069
Study Section
Neurology B Subcommittee 1 (NEUB)
Project Start
1986-08-01
Project End
1989-07-31
Budget Start
1986-08-01
Budget End
1987-07-31
Support Year
1
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Texas Medical Br Galveston
Department
Type
Schools of Medicine
DUNS #
041367053
City
Galveston
State
TX
Country
United States
Zip Code
77555
Kadekaro, M (2004) Nitric oxide modulation of the hypothalamo-neurohypophyseal system. Braz J Med Biol Res 37:441-50
Kadekaro, M; Terrell, M L; Bui, V et al. (2001) Central interactions between angiotensin II and PGD(2) in the regulation of vasopressin and oxytocin secretion in dehydrated rats. Brain Res 889:84-8
Summy-Long, J Y; Kadekaro, M (2001) Role of circumventricular organs (CVO) in neuroendocrine responses: interactions of CVO and the magnocellular neuroendocrine system in different reproductive states. Clin Exp Pharmacol Physiol 28:590-601
Kadekaro, M; Terrell, M L; Liu, H et al. (2000) Indomethacin prevents the L-NAME-induced increase in plasma levels of oxytocin in dehydrated rats. Brain Res 877:371-3
Kadekaro, M; Summy-Long, J Y (2000) Centrally produced nitric oxide and the regulation of body fluid and blood pressure homeostases. Clin Exp Pharmacol Physiol 27:450-9
Summy-Long, J Y; Bui, V; Gestl, S et al. (1998) Effects of central injection of kyotorphin and L-arginine on oxytocin and vasopressin release and blood pressure in conscious rats. Brain Res Bull 45:395-403
Liu, H; Terrell, M L; Summy-Long, J Y et al. (1998) Brain ANG II and prostaglandins mediate the pressor response after central blockade of nitric oxide synthase. Brain Res 785:317-28
Liu, H; Terrell, M L; Bui, V et al. (1998) Nitric oxide control of drinking, vasopressin and oxytocin release and blood pressure in dehydrated rats. Physiol Behav 63:763-9
Kadekaro, M; Terrell, M L; Liu, H et al. (1998) Effects of L-NAME on cerebral metabolic, vasopressin, oxytocin, and blood pressure responses in hemorrhaged rats. Am J Physiol 274:R1070-7
Kadekaro, M; Liu, H; Terrell, M L et al. (1997) Role of NO on vasopressin and oxytocin release and blood pressure responses during osmotic stimulation in rats. Am J Physiol 273:R1024-30

Showing the most recent 10 out of 29 publications