1.Increased atria expression of receptor activity-modifying proteins in heart failure patients.
Yu-fang WANG ; Ji ZHANG ; Jing LI ; Li-qiong LAN ; Zhi-mei YANG ; Shu-ren WANG
Chinese Journal of Medical Genetics 2004;21(4):351-354
OBJECTIVEReceptor activity-modifying proteins (RAMPs) determine the ligand specificity of the calcitonin receptor-like receptor (CRLR); co-expression of RAMP1 and CRLR results in a calcitonin gene related peptide (CGRP) receptor, whereas the association of RAMP2 or RAMP3 with CRLR gives an adrenomedullin(ADM) receptor. As CGRP and ADM may play a beneficial role in heart failure, this study aimed at the question whether RAMPs mRNAs are changed in heart failure.
METHODSSemi-quantitative reverse transcription-PCR (RT-PCR) was used to detect and quantify the mRNAs of RAMP1 and RAMP3 in the atria of heart failing patients.
RESULTSIt was found that the expressions of RAMP1, RAMP2 and RAMP3 mRNAs increased with the worsening of heart function, but the expressions of RAMP1 and RAMP2 mRNA decreased at level IV of heart failure.
CONCLUSIONThe above results demonstrated in the atria of heart failure patients an up-regulation of CGRP receptor by an increase of RAMP1 in association with CRLR and an up-regulation of ADM receptor by an increase of RAMP2 expression in association with CRLR, thus suggesting that CGRP and ADM receptors be playing a functional role in compensating the chronic heart failure in human.
Adult ; Calcitonin Receptor-Like Protein ; Female ; Heart Atria ; metabolism ; Heart Failure ; genetics ; physiopathology ; Humans ; Intracellular Signaling Peptides and Proteins ; genetics ; physiology ; Male ; Membrane Proteins ; genetics ; physiology ; Receptor Activity-Modifying Protein 1 ; Receptor Activity-Modifying Protein 2 ; Receptor Activity-Modifying Protein 3 ; Receptor Activity-Modifying Proteins ; Receptors, Adrenomedullin ; Receptors, Calcitonin ; genetics ; physiology ; Receptors, Calcitonin Gene-Related Peptide ; genetics ; physiology ; Receptors, Peptide ; genetics ; physiology ; Reverse Transcriptase Polymerase Chain Reaction
2.Expression of adrenomedullin and its receptor mRNA in the tissues of normal adrenal medulla and pheochromocytoma.
Dong-Mei LIU ; Zheng-Pei ZENG ; Han-Zhong LI ; Xin-Rong FAN ; Guo-Qiang LIU ; Wei-Gang YAN ; An-Li TONG ; Xin ZHENG
Acta Academiae Medicinae Sinicae 2005;27(4):452-456
OBJECTIVETo investigate the expression of human adrenomedullin (ADM) and its receptor-receptor activity modifying protein 2/calcitonin receptor-like receptor (RAMP2/CRLR) mRNA in the tissues of normal adrenal medulla and pheochromocytoma.
METHODSTotal RNA was extracted from normal adrenal medulla and pheochromocytomas. The expression of ADM and RAMP2/CRLR mRNA were studied by reverse transcription-polymerase chain reaction. The ratios of ADM/GAPDH, RAMP2/ GAPDH, CRLR/GAPDH were used to evaluate the expression levels of ADM, RAMP2 and CRLR mRNA.
RESULTSExpressions of ADM and its receptor- RAMP2/CRLR mRNA were detected in normal adrenal medulla and pheochromocytoma tissues. ADM/GAPDH were 0.48+/-0.09 and 0.75+/-0.24, RAMP2/ GAPDH 0.79+/-0.12 and 1.29+/-0.30, CRLR/GAPDH 0.40+/-0.08 and 0.87+/-0.22 in normal adrenal medulla and pheochromocytomas, respectively (P < 0.05).
CONCLUSIONADM exerts a possible autocrine or paracrine effect in the adrenal. ADM may be involved in the pathogenesis of pheochromocytoma.
Adrenal Gland Neoplasms ; metabolism ; Adrenal Medulla ; metabolism ; Adrenomedullin ; Adult ; Calcitonin Gene-Related Peptide ; biosynthesis ; genetics ; Female ; Humans ; Intracellular Signaling Peptides and Proteins ; genetics ; Male ; Membrane Proteins ; biosynthesis ; genetics ; Middle Aged ; Peptides ; genetics ; metabolism ; Pheochromocytoma ; metabolism ; RNA, Messenger ; biosynthesis ; genetics ; Receptor Activity-Modifying Protein 2 ; Receptor Activity-Modifying Proteins ; Receptors, Adrenomedullin ; Receptors, Calcitonin ; biosynthesis ; genetics ; Receptors, Peptide ; metabolism
3.Changes in adrenomedullin and receptor activity-modifying protein 2 mRNA in myocardium and vessels during L-NNA-induced hypertension in rats.
Yong-Fen QI ; Yan-Rong SHI ; Ding-Fang BU ; Hong-Feng JIANG ; Lin GAO ; Yong-Zheng PANG ; Chao-Shu TANG
Acta Physiologica Sinica 2002;54(4):337-341
To explore the changes in adrenomedullin (ADM) and receptor activity-modifying protein 2 (RAMP2) mRNA in myocardium and vessels in hypertension, a hypertensive rat model was prepared by administering L-NNA. Contents of ADM in plasma, myocardium and vessels were measured by radioimmunoassay (RIA). The levels of pro-ADM mRNA of myocardium and vessels were determined by competitive quantitative RT-PCR. The results showed that L-NNA induced hypertension and cardiomegaly. The ratio of heart to body weight increased by 35.5% (P<0.01). In hypertensive rats the ir-ADM in plasma, myocardium and vessels was increased by 80%, 72% and 57% (P<0.01), respectively compared with the control. The amounts of ADM mRNA in myocardium and vessels were increased by 50% and 109.2% (P<0.05), respectively, and the amounts of RAMP2 mRNA was increased by 132% and 87% (P<0.01), respectively, compared with control. The levels of ADM in myocardium and vessels were positively correlated with RAMP2 mRNA, the correlation coefficients were 0.741 and 0.885 (P<0.01), respectively. The results obtained indicate that in hypertensive rats, ADM is elevated in plasma, myocardium and ves-myocardium and vessel, and ADM and RAMP2 mRNA are up-regulated in myocardium and vessel. The ADM/RAMP2 system may play an important role in the pathogenesis of hypertension.
Adrenomedullin
;
metabolism
;
Animals
;
Cardiomegaly
;
chemically induced
;
metabolism
;
Hypertension
;
chemically induced
;
metabolism
;
Myocardium
;
metabolism
;
Nitroarginine
;
pharmacology
;
RNA, Messenger
;
Rats
;
Receptor Activity-Modifying Protein 2
;
metabolism
;
Reverse Transcriptase Polymerase Chain Reaction
;
Up-Regulation
4.Effect and mechanism of intermedin in acute rat cardiac ischemic injury.
Qiu-Xiang DU ; Wei YUE ; Ying-Yuan WANG
Journal of Forensic Medicine 2011;27(3):164-168
OBJECTIVE:
To investigate the effect and potential mechanism of intermedin (IMD) in acute cardiac ischemic injury and to provide a new approach for exploring mechanism of sudden cardiac death.
METHODS:
Seventy-two healthy male rats were randomly divided into 3 groups: control, ischemic and the IMD-treated group. The activity of lactate dehydrogenase (LDH), malondialdehyde (MDA) and superoxide dismutase (SOD) in heart blood were tested by enzyme chemistry method. The mRNA changes of calcitonin receptor-like receptor (CRLR) and receptor activity-modifying proteins (RAMPs) in cardiac were measured by real-time PCR analysis. Myocardial cyclic adenosine monophosphate (cAMP) content was determined by enzyme linked immunosorbent assay (ELISA). Apoptosis related factors Bcl-2 and Bax were detected by immunohistochemistry.
RESULTS:
Comparing with the control group, LDH and MDA activity of ischemic group in heart blood increased and SOD activity decreased. The concentration of cAMP increased in ventricular muscle, Bcl-2 and Bax proteins expression ratio level decreased. The intravenation of IMD decreased the level of increased activity of LDH and MDA, and lessened the level of decreased activity of SOD. The mRNA expression of CRLR and RAMPs obviously increased in ventricular muscle.
CONCLUSION
The protective effect of IMD against myocardial ischemic injury could be caused by decreasing the oxidative stress of ischemia and inhibiting the myocardial apoptosis.
Adrenomedullin/pharmacology*
;
Animals
;
Apoptosis/drug effects*
;
Calcitonin Receptor-Like Protein/metabolism*
;
Cardiotonic Agents/pharmacology*
;
Cyclic AMP/metabolism*
;
Disease Models, Animal
;
L-Lactate Dehydrogenase/metabolism*
;
Male
;
Malondialdehyde/metabolism*
;
Myocardial Ischemia/pathology*
;
Myocardium/pathology*
;
Neuropeptides/pharmacology*
;
Proto-Oncogene Proteins c-bcl-2/metabolism*
;
RNA, Messenger/metabolism*
;
Random Allocation
;
Rats
;
Rats, Sprague-Dawley
;
Real-Time Polymerase Chain Reaction
;
Receptor Activity-Modifying Proteins/metabolism*
;
Superoxide Dismutase/metabolism*