Systemic hypoxia is a potentially lethal situation for the animal. To protect major organs from irreversible damage, the carotid body, a primary arterial chemosensory organ, sends a message to the brain and induces various systemic responses. The mechanisms of hypoxic chemotransmission in the carotid body is not still clear, but the involvement of K+ channels and neurotransmitters has been indicated. Studies have shown that acetylcholine (ACh) plays an active role in the excitation of glomus cells. Accordingly, we hypothesized that interaction between ACh and voltage-gated K+ (Kv) channels plays an important role in the excitation of glomus cells. Our preliminary studies showed that low doses of ACh enhanced and high doses of ACh inhibited Kv current in cat glomus cells. We will extend these studies and investigate mechanisms involved in the modulation of Kv channels by ACh. Patch clamp, microfluorometric, gene expression array, RT-PCR and immunocytochemical techniques will be applied. Initially we will use our cat model, because we have already characterized Kv channels and cholinergic receptors in cat glomus cells. Contribution of nicotinic, muscarinic M1 and M2 receptors to the modulation of Kv current in relation to cytosolic Ca2+, PKC and tyrosine kinase will be investigated. These studies will reveal how the interaction between ACh and Kv channels occurs at subcellular level (Specific Aim 1). Subsequently, we will extend our studies to a mouse model (DBA/2J and A/J strains). Hypoxic ventilatory responses and glomus cell responses to ACh in these strains are substantially different. We have hypothesized that variations in cholinergic modulation of Kv channels are the bases of these differences (Specific aim 2). The studies in mice will show whether these differences are genetically controlled. The proposed studies will give new insight into mechanisms of the carotid body excitation. In the perspective of public health, understanding the chemosensory and chemotransductive mechanisms may be valuable for the treatment of some pathological conditions related to carotid body function such as primary hypertension, obstructive sleep apnea, abnormal ventilation in Prader-Willi syndrome, sudden infant death syndrome and congenital central hypoventilation syndrome. These diseases are known to have a genetic basis.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL072293-03
Application #
6924678
Study Section
Respiratory Physiology Study Section (RESP)
Program Officer
Twery, Michael
Project Start
2003-09-01
Project End
2007-06-30
Budget Start
2005-07-01
Budget End
2006-06-30
Support Year
3
Fiscal Year
2005
Total Cost
$245,250
Indirect Cost
Name
Johns Hopkins University
Department
Public Health & Prev Medicine
Type
Schools of Public Health
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Fitzgerald, Robert S; Shirahata, Machiko; Chang, Irene et al. (2012) Hydrogen sulfide acting at the carotid body and elsewhere in the organism. Adv Exp Med Biol 758:241-7
Kostuk, Eric W; Balbir, Alexander; Fujii, Koichi et al. (2012) Divergent postnatal development of the carotid body in DBA/2J and A/J strains of mice. J Appl Physiol 112:490-500
Fitzgerald, Robert S; Shirahata, Machiko; Chang, Irene et al. (2011) The impact of hydrogen sulfide (H?S) on neurotransmitter release from the cat carotid body. Respir Physiol Neurobiol 176:80-9
Fitzgerald, Robert S; Shirahata, Machiko; Chang, Irene et al. (2009) The impact of hypoxia and low glucose on the release of acetylcholine and ATP from the incubated cat carotid body. Brain Res 1270:39-44
Igarashi, A; Zadzilka, N; Shirahata, M (2009) Benzodiazepines and GABA-GABAA receptor system in the cat carotid body. Adv Exp Med Biol 648:169-75
Balbir, Alexander; Lande, Boris; Fitzgerald, Robert S et al. (2008) Behavioral and respiratory characteristics during sleep in neonatal DBA/2J and A/J mice. Brain Res 1241:84-91
Balbir, Alexander; Lee, Hannah; Okumura, Mariko et al. (2007) A search for genes that may confer divergent morphology and function in the carotid body between two strains of mice. Am J Physiol Lung Cell Mol Physiol 292:L704-15
Fitzgerald, Robert S; Shirahata, Machiko; Balbir, Alexander et al. (2007) Oxygen sensing in the carotid body and its relation to heart failure. Antioxid Redox Signal 9:745-9
Shirahata, Machiko; Balbir, Alexander; Otsubo, Toshiki et al. (2007) Role of acetylcholine in neurotransmission of the carotid body. Respir Physiol Neurobiol 157:93-105
Yamaguchi, Shigeki; Balbir, Alexander; Okumura, Mariko et al. (2006) Genetic influence on carotid body structure in DBA/2J and A/J strains of mice. Adv Exp Med Biol 580:105-9; discussion 351-9

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