Vascular smooth muscle (VSM) and endothelium play primary roles in pregnancy-associated vascular adaptations. Peptides of the calcitonin gene-related peptide (CGRP)-family-CGRP, adrenomedullin (AM), and intermedin (IMD)-have been shown to play significant roles in these adaptations. CGRP, AM, and IMD share common receptor components, calcitonin receptor-like receptor (CRLR) and receptor activity modifying protein (RAMP)1, 2, and 3, in different combinations in exerting their biological functions. During the previous funding periods, we have demonstrated that CGRP, AM, and IMD play critical roles in regulating pregnancy-associated vascular adaptations, utero placental functions, and fetal growth. Interestingly, the effect of these peptides varied depending on the vascular bed and between VSM and endothelial cells. Our new preliminary findings suggest variable associations and competitive interactions of RAMPs with CRLR could contribute to the observed differences in peptide-induced relaxation between mesenteric artery (MA) and uterine artery (UA). Tumor necrosis factor- ? (TNF) caused differential and selective decreases in RAMPs or CRLR in VSM and endothelial cells. We hypothesize that differences in vasorelaxations to CGRP, AM, and IMD in both MA and UA are determined by differential association and competitive interaction of different RAMPs with CRLR and that these associations and interactions are cell-specifically downregulated by TNF?. We will utilize intracellular cAMP measurements, shRNA-mediated receptor knockdowns, novel proximity ligation assay (in situ method to quantitatively detect CRLR and RAMP protein proximity associations at the cell membrane level), and functional vascular reactivity studies to test our hypotheses.
Four specific aims are proposed.
Specific Aim 1 : To investigate molecular mechanisms of action for 3 peptides of the CGRP family on MA VSM cells. We will determine competitive association of specific RAMPs with CRLR and cAMP generation in MA VSM cells and vasorelaxation responses to peptides in MA rings with knockdown of specific RAMPs.
Specific Aim 2 : To assess molecular mechanisms of action for 3 peptides of the CGRP family on UA VSM cells. We will determine association of RAMPs with CRLR and cAMP generation in UA VSM and relaxation response to peptides in UA rings with knockdown of specific RAMPs.
Specific Aim 3 : To investigate expression and association of RAMPs with CRLR in endothelial cells and assess effects of 3 peptides on eNOS expression and phosphorylation and NO production.
Specific Aim 4 : To determine if TNF? alters expression and molecular interactions of RAMPs and CRLR and, therefore, actions of 3 peptides in VSM and endothelial cells. These findings will significantly advance our knowledge of molecular mechanisms underlying CGRP family peptide-induced vascular adaptations and offer important original insights into the possible mechanisms of vascular dysfunction in pathological pregnancies.

Public Health Relevance

Preeclampsia is a major medical disorder occurring during pregnancy and brings about more than 50,000 maternal deaths worldwide, with an estimated 45,000 deaths in the US alone. While the biological mechanisms of preeclampsia are unknown, we will investigate the molecular mechanisms of vascular adaptations that occur during pregnancy and seek understanding in how these adaptations may fail, resulting in preeclampsia. Our investigation will focus on the calcitonin gene-related peptide family and its role in these processes, with the goal of using these new mechanistic studies to develop approaches to prevent and treat preeclampsia, and to thereby reduce in women morbidity and mortality related to the cardiovascular system.

National Institute of Health (NIH)
Research Project (R01)
Project #
Application #
Study Section
Pregnancy and Neonatology Study Section (PN)
Program Officer
Ershow, Abby
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
Baylor College of Medicine
Obstetrics & Gynecology
Schools of Medicine
United States
Zip Code
Blesson, Chellakkan S; Chinnathambi, Vijayakumar; Hankins, Gary D et al. (2015) Prenatal testosterone exposure induces hypertension in adult females via androgen receptor-dependent protein kinase C?-mediated mechanism. Hypertension 65:683-90
Blesson, Chellakkan S; Sathishkumar, Kunju; Chinnathambi, Vijayakumar et al. (2014) Gestational protein restriction impairs insulin-regulated glucose transport mechanisms in gastrocnemius muscles of adult male offspring. Endocrinology 155:3036-46
Chinnathambi, Vijayakumar; Blesson, Chellakkan S; Vincent, Kathleen L et al. (2014) Elevated testosterone levels during rat pregnancy cause hypersensitivity to angiotensin II and attenuation of endothelium-dependent vasodilation in uterine arteries. Hypertension 64:405-14
Chinnathambi, Vijayakumar; More, Amar S; Hankins, Gary D et al. (2014) Gestational exposure to elevated testosterone levels induces hypertension via heightened vascular angiotensin II type 1 receptor signaling in rats. Biol Reprod 91:6
Gao, Haijun; Liebenthal, Daniel A; Yallampalli, Uma et al. (2014) Adrenomedullin promotes rat trophoblast stem cell differentiation. Biol Reprod 91:65
Banadakoppa, Manu; Liebenthal, Daniel; Nowak, David E et al. (2013) Role of transcription factor Sp1 and RNA binding protein HuR in the downregulation of Dr+ Escherichia coli receptor protein decay accelerating factor (DAF or CD55) by nitric oxide. FEBS J 280:840-54
Gao, Haijun; Yallampalli, Uma; Yallampalli, Chandra (2013) Gestational protein restriction affects trophoblast differentiation. Front Biosci (Elite Ed) 5:591-601
Chinnathambi, Vijayakumar; Balakrishnan, Meena; Ramadoss, Jayanth et al. (2013) Testosterone alters maternal vascular adaptations: role of the endothelial NO system. Hypertension 61:647-54
Havemann, Dara; Balakrishnan, Meena; Borahay, Mostafa et al. (2013) Intermedin/adrenomedullin 2 is associated with implantation and placentation via trophoblast invasion in human pregnancy. J Clin Endocrinol Metab 98:695-703
Yallampalli, Chandra; Chauhan, Madhu; Sathishkumar, K (2013) Calcitonin gene-related family peptides in vascular adaptations, uteroplacental circulation, and fetal growth. Curr Vasc Pharmacol 11:641-54

Showing the most recent 10 out of 28 publications