The objective of this proposal is to characterize the receptors, signaling pathways and cellular mechanisms involved in relaxation of gastric smooth muscle by peptide (VIP, PACAP) and non-peptide (NO) neurotransmitters of the myenteric plexus. Several advances made during the previous funding period form the basis of the proposal. We have identified two receptor types for which VIP and PACAP have high affinity: a cognate, seven-transmembrane VIP2/PACAP3 receptor coupled via GS to adenylyl cyclase, and a distinct, single-transmembrane natriuretic peptide clearance receptor (NPR-C) coupled via Gi1 and Gi2 to activation of a constitutive NO synthase (NOS) in smooth muscle cells. We have identified the NOS isoform as eNOS by RT-PCR in muscle cultures and by in situ RT-PCR in single muscle cells. The concurrent stimulation of cAMP and cGMP has important implications with respect to their regulation by specific phosphodiesterases (PDE), activation and cross-activation of cA-kinase and cG-kinase, and feedback regulation of adenylyl cyclase. Preliminary studies have identified the isoforms of PDE (PDE3, PDE4, PDE5) and adenylyl cyclase (types V and VI) expressed in gastric muscle. Accordingly, the first aim is to characterize NPR-C and VIP2/PACAP3 receptors: the studies involve experiments in eNOS minus/minus and NPR-C minus/minus mice, reconstitution studies in COS-1 cells co-transfected with NPR-C and eNOS, site-directed mutagenesis to identify binding and G protein coupling domains, and chimeric constructs and site-directed mutagenesis to identify VIP2/PACAP3 receptor subtypes.
The second aim i s to characterize the regulation of adenylyl cyclases V/VI by cA-kinase, G proteins and Ca2+ influx; and the regulation of cAMP levels by cAMP-specific PDE4 and PDE3 and cGMP levels by cGMP- specific PDE5.
The third aim i s to characterize the concurrent activation and cross-activation of cA- and cG-kinase, and their role in phosphorylation of major targets in smooth muscle, including PLC-beta and PLA2, IP3 and ryanodine receptors, and MLC phosphatase. The combined approach embodied by these aims, all of which are supported by preliminary studies, should advance our knowledge of the cellular mechanisms mediating visceral smooth muscle relaxation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK028300-20
Application #
6177351
Study Section
Special Emphasis Panel (ZRG2-RAP (02))
Program Officer
May, Michael K
Project Start
1984-04-01
Project End
2004-03-31
Budget Start
2000-04-01
Budget End
2001-03-31
Support Year
20
Fiscal Year
2000
Total Cost
$198,738
Indirect Cost
Name
Virginia Commonwealth University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
City
Richmond
State
VA
Country
United States
Zip Code
23298
Mahavadi, Sunila; Grider, John R; Murthy, Karnam S (2018) Muscarinic m2 receptor-mediated actin polymerization via PI3 kinase ? and integrin-linked kinase in gastric smooth muscle. Neurogastroenterol Motil :e13495
Mahavadi, Sunila; Nalli, Ancy D; Wang, Hongxia et al. (2018) Regulation of gastric smooth muscle contraction via Ca2+-dependent and Ca2+-independent actin polymerization. PLoS One 13:e0209359
May, Alexander T; Crowe, Molly S; Blakeney, Bryan A et al. (2018) Identification of expression and function of the glucagon-like peptide-1 receptor in colonic smooth muscle. Peptides 112:48-55
Blakeney, Bryan A; Crowe, Molly S; Mahavadi, Sunila et al. (2018) Branched Short-Chain Fatty Acid Isovaleric Acid Causes Colonic Smooth Muscle Relaxation via cAMP/PKA Pathway. Dig Dis Sci :
Qian, Jie; Mummalaneni, Shobha; Phan, Tam-Hao T et al. (2017) Cyclic-AMP regulates postnatal development of neural and behavioral responses to NaCl in rats. PLoS One 12:e0171335
Nalli, Ancy D; Bhattacharya, Sayak; Wang, Hongxia et al. (2017) Augmentation of cGMP/PKG pathway and colonic motility by hydrogen sulfide. Am J Physiol Gastrointest Liver Physiol 313:G330-G341
Parikh, Jay; Zemljic-Harpf, Alice; Fu, Johnny et al. (2017) Altered Penile Caveolin Expression in Diabetes: Potential Role in Erectile Dysfunction. J Sex Med 14:1177-1186
Nalli, Ancy D; Wang, Hongxia; Bhattacharya, Sayak et al. (2017) Inhibition of RhoA/Rho kinase pathway and smooth muscle contraction by hydrogen sulfide. Pharmacol Res Perspect 5:
Mahavadi, Sunila; Sriwai, Wimolpak; Manion, Olivia et al. (2017) Diabetes-induced oxidative stress mediates upregulation of RhoA/Rho kinase pathway and hypercontractility of gastric smooth muscle. PLoS One 12:e0178574
Qian, Jie; Mummalaneni, Shobha K; Alkahtani, Reem M et al. (2016) Nicotine-Induced Effects on Nicotinic Acetylcholine Receptors (nAChRs), Ca2+ and Brain-Derived Neurotrophic Factor (BDNF) in STC-1 Cells. PLoS One 11:e0166565

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