ABSTRACT
OBJECTIVES@#To study the role of adrenomedullin (ADM) in hyperoxia-induced lung injury by examining the effect of ADM on the expression of calcitonin receptor-like receptor (CRLR), receptor activity-modifying protein 2 (RAMP2), extracellular signal-regulated kinase (ERK), and protein kinase B (PKB) in human pulmonary microvascular endothelial cells (HPMECs) under different experimental conditions.@*METHODS@#HPMECs were randomly divided into an air group and a hyperoxia group (@*RESULTS@#Compared with the air group, the hyperoxia group had significant increases in the mRNA and protein expression levels of ADM, CRLR, RAMP2, ERK1/2, and PKB (@*CONCLUSIONS@#ERK1/2 and PKB may be the downstream targets of the ADM signaling pathway. ADM mediates the ERK/PKB signaling pathway by regulating CRLR/RAMP2 and participates in the protection of hyperoxia-induced lung injury.
Subject(s)
Humans , Adrenomedullin/genetics , Endothelial Cells , Hyperoxia/complications , Lung Injury , Receptor Activity-Modifying ProteinsABSTRACT
Abstract Objective: We aimed to investigate the protective effect of adrenomedullin (ADM) on cerebral tissue of rats with cerebral ischemia/reperfusion (I/R) injury. Methods: Thirty-two Wistar rats were randomized into four groups (n=8). In the I/R Group, bilateral common carotid arteries were clamped for 30 minutes and, subsequently, reperfused for 120 minutes. In the ADM Group, rats received 12 µg/kg of ADM. In the I/R+ADM Group, bilateral common carotid arteries were clamped for 30 minutes and, subsequently, the rats received 12 µg/ kg of ADM. Then, reperfusion was performed for 120 minutes. The Control Group underwent no procedure. Blood and brain tissue samples were collected for biochemical and histopathological analysis. Serum malondialdehyde (MDA), superoxide dismutase (SOD), and glutathione peroxidase (GPx) were analysed. Brain tissue was evaluated histopathologically and neuronal cells were counted in five different fields, at a magnification of ×400. Results: Brain MDA in I/R Group was significantly higher than in ADM Group. Brain GPx and SOD in I/R+ADM Group were significantly higher than in I/R Group. The number of neurons was decreased in I/R Group compared to the Control Group. The number of neurons in I/R+ADM Group was significantly higher than in I/R Group, and lower than in Control Group. Apoptotic changes decreased significantly in I/R+ADM Group and the cell structure was similar in morphology compared to the Control Group. Conclusion: We demonstrated the cerebral protective effect of ADM in the rat model of cerebral I/R injury after bilateral carotid artery occlusion.
Subject(s)
Animals , Rats , Carotid Artery, Common , Reperfusion , Reperfusion Injury/prevention & control , Rats, Wistar , AdrenomedullinABSTRACT
Intermedin/adrenomedullin-2 (IMD/AM2), a member of the calcitonin gene-related peptide/AM family, plays an important role in protecting the cardiovascular system. However, its role in the enhanced sympathoexcitation in obesity-related hypertension is unknown. In this study, we investigated the effects of IMD in the paraventricular nucleus (PVN) of the hypothalamus on sympathetic nerve activity (SNA), and lipopolysaccharide (LPS)-induced sympathetic activation in obesity-related hypertensive (OH) rats induced by a high-fat diet for 12 weeks. Acute experiments were performed under anesthesia. The dynamic alterations of sympathetic outflow were evaluated as changes in renal SNA and mean arterial pressure (MAP) in response to specific drugs. Male rats were fed a control diet (12% kcal as fat) or a high-fat diet (42% kcal as fat) for 12 weeks to induce OH. The results showed that IMD protein in the PVN was downregulated, but Toll-like receptor 4 (TLR4) and plasma norepinephrine (NE, indicating sympathetic hyperactivity) levels, and systolic blood pressure were increased in OH rats. LPS (0.5 µg/50 nL)-induced enhancement of renal SNA and MAP was greater in OH rats than in obese or control rats. Bilateral PVN microinjection of IMD (50 pmol) caused greater decreases in renal SNA and MAP in OH rats than in control rats, and inhibited LPS-induced sympathetic activation, and these were effectively prevented in OH rats by pretreatment with the AM receptor antagonist AM22-52. The mitogen-activated protein kinase/extracellular signal-regulated kinase (ERK) inhibitor U0126 in the PVN partially reversed the LPS-induced enhancement of SNA. However, IMD in the PVN decreased the LPS-induced ERK activation, which was also effectively prevented by AM22-52. Chronic IMD administration resulted in significant reductions in the plasma NE level and blood pressure in OH rats. Moreover, IMD lowered the TLR4 protein expression and ERK activation in the PVN, and decreased the LPS-induced sympathetic overactivity. These results indicate that IMD in the PVN attenuates SNA and hypertension, and decreases the ERK activation implicated in the LPS-induced enhancement of SNA in OH rats, and this is mediated by AM receptors.
Subject(s)
Animals , Male , Adrenomedullin , Metabolism , Blood Pressure , Physiology , Hypertension , Lipopolysaccharides , Pharmacology , Neuropeptides , Metabolism , Obesity , Rats, Sprague-Dawley , Receptors, Adrenomedullin , Metabolism , Sympathetic Nervous System , Metabolism , Toll-Like Receptor 4 , MetabolismABSTRACT
The pain peptide adrenomedullin (AM) plays a pivotal role in pathological pain. The present study was designed to investigate the effect of blockade of AM receptor on bone cancer pain (BCP) and its mechanism. BCP was developed by inoculation of Walker 256 mammary gland carcinoma cells in the tibia medullary cavity of Sprague Dawley rats. The selective AM receptor antagonist AMwas administered intrathecally on 15 d after the inoculation. Quantitative real-time PCR was used to detect mRNA level of CC chemokine ligand 2 (CCL2) in dorsal root ganglion (DRG). Double immunofluorescence staining was used to analyze the localizations of CCL2 and AM in DRG of normal rats. The results showed that, from 6 to15 d after the inoculation, the animals showed significant reduction in the mechanical pain threshold in the ipsilateral hindpaw, companied by the decline in bone density of tibia bone. The expression of CCL2 mRNA in DRG of BCP rats was increased by 3 folds (P < 0.001 vs saline group). Intrathecal administration of AMabolished bone cancer-induced mechanical allodynia and increase of CCL2 mRNA level (P < 0.001). In normal rats, CCL2 was co-localized with AM in DRG neurons. These results suggest that AM may play a role in the pathogenesis of BCP. The increased AM bioactivity up-regulates CCL2 expression in DRG, which may contribute to the induction of pain hypersensitivity in bone cancer.
Subject(s)
Animals , Rats , Adrenomedullin , Pharmacology , Bone Neoplasms , Drug Therapy , Chemokine CCL2 , Metabolism , Ganglia, Spinal , Hyperalgesia , Drug Therapy , Pain , Drug Therapy , Pain Threshold , Peptide Fragments , Pharmacology , Rats, Sprague-Dawley , Real-Time Polymerase Chain Reaction , Receptors, AdrenomedullinABSTRACT
La adrenomedulina (AM) es un péptido involucrado en la regulación cardiovascular. En el cerebelo, la densidad de los receptores de la AM se encuentra alterada durante la hipertensión, sugiriendo un posible papel del sistema adrenomedulinérgico cerebelar en la regulación de la presión arterial (PA). El objetivo del presente estudio fue evaluar el efecto funcional in vivo de la AM durante el estrés agudo, mediante la administración in situ de AM en el vermis cerebelar de la rata. Se emplearon ratas adultas normotensas Wistar Kyoto (WKY) y Sprague Dawley (SD) y ratas espontáneamente hipertensas (SHR) las cuales fueron anestesiadas y posteriormente canuladas en el vermis cerebelar. El estrés se indujo mediante el uso del estímulo eléctrico plantar (EEP). Los animales fueron divididos en grupos que recibieron AM (0,2 o 200 pmol/5μL) o vehículo (solución fisiológica, 5μL). La PA se determinó antes del experimento y después de la administración del tratamiento respectivo, seguida de la aplicación del EEP (100 V, 5 Hz, 10 mseg, durante 4 minutos). La PA se determinó mediante pletismografía digital no invasiva. Los resultados demuestran que la microinyección de AM (0,2 y 200 pmol) in situ en el vermis cerebeloso en ratas SD, WKY y SHR disminuye significativamente la respuesta presora frente al estrés inducido por el EEP, lo que sugiere que la acción hipotensora está mediada a través de la regulación del eflujo simpático. Estos hallazgos demuestran la participación de la AM cerebelosa en la regulación de la respuesta cardiovascu lar frente al estrés.
Adrenomedullin (AM) is a peptide involved in cardiovascular regulation. In the cerebellum, the density of AM receptors is altered during hypertension, suggesting a pos sible role of cerebellar adrenomedulinergic system in the regulation of blood pressure (BP). The aim of this study was to evaluate the functional role of AM during acute stress, by in situ administration of AM into the cerebellar vermis in rats. Adult normotensive Wistar Kyoto (WKY) and Sprague Dawley (SD) rats and spontaneously hypertensive rats (SHR), were anes thetized and their cerebellar vermis cannulated. Footshock was used as stressor. Animals were divided into groups that received either AM (0.2 and 200 pmol/5μL) or vehicle (physiological saline, 5μL). The BP was determined, using noninvasive digital plethysmography, before and after treatment, followed by footshock (100V, 5 Hz, 10 msec, for 4 minutes). The results show that microinjection of AM (0.2 and 200 pmol) in situ into the cerebellar vermis in SD, WKY and SHR rats, significantly decreased the pressor response induced by footshock stress, sugges ting that the hypotensive action is mediated through regulation of sympathetic outflow. Taken together, our results demonstrate a role of cerebellar AM in the regulation of cardiovascular response to stress.
Subject(s)
Animals , Male , Stress, Physiological/physiology , Cerebellum/physiology , Adrenomedullin/physiology , Rats, Wistar , Rats, Sprague-DawleyABSTRACT
La adrenomedulina (ADM), péptido vasodilatador de 52 aminoácidos, ubícuo, posee múltiples efectos fisiológicos que contribuyen a respuestas homeostáticas. Se encuentra en concentraciones importantes en la glándula suprarrenal, el pulmón, el sistema cardiovascular y el renal. Ejerce acciones biológicas a través de sus receptores AM1 y AM2, heterodímeros constituidos por el receptor semejante al receptor de calcitonina (CLR) y proteínas modificadoras de la actividad del receptor (RAMPs), CLR/RAMP2 y CLR/RAMP3, respectivamente. La principal vía de señalización es la adenilato ciclasa/AMPc en patologías cardiovasculares y renales, así como en la sepsis. Los niveles plasmáticos de ADM se elevan proporcionalmente con el incremento de la presión sanguínea y con el grado de daño renal, en pacientes con hipertensión arterial; así mismo, dichos niveles se correlacionan con el grado de hipertrofia cardíaca y arterial. La ADM tiene efectos renales, tubulares, ya que tiene acción diurética y natriurética; posee efectos vasodilatadores que producen aumento de la tasa de filtración glomerular y del flujo sanguíneo renal. Este péptido inhibe la proliferación y la generación de radicales libres en células mesangiales; actúa inhibiendo la secreción de aldosterona en la zona glomerulosa y de endotelina-1 en células musculares lisas vasculares. Se ha propuesto como marcador de riesgo en diversas patologías, especialmente en la insuficiencia renal crónica; en esta patología, que cursa con hipertrofia compensadora de los glomérulos y proliferación del mesangio, la administración de ADM disminuye los niveles de proteinuria, lo que sugiere que además de un importante rol modulador en la presión arterial, pudiera ser una opción terapéutica para la insuficiencia renal crónica.
Adrenomedullin (AM) is a potent vasodilatory 52-aminoacid peptide hormone, ubiquitous with multiple physiological effects which contribute to homeostatic responses. Significantly, it is distributed in the adrenal gland, lung, cardiovascular and renal system. The biological effects of AM are directly mediated by specific receptors as heterodimers composed of the calcitonin-receptor-like receptor (CLR) and one of two receptor activity modifying proteins (RAMP2 or RAMP3). The CLR/RAMP2 (AM1 receptor) is more highly AM-specific than The CLR/RAMP3 (AM2 receptor). Plasma levels of AM are elevated proportionately to the increase in blood pressure and degree of renal damage in patients with hypertension; likewise, these levels are correlated with the degree of heart and arterial hypertrophy. AM has renal vasodilatory, natriuretic and diuretic actions; increased glomerular filtration rate and renal blood flow. AM inhibits proliferation and reactive oxygen species generation in mesangial cells; also inhibits aldosterone secretion in the zona glomerulosa and endothelin-1 in vascular smooth muscle cells. Therefore, it is proposed as a new marker in various diseases, especially chronic renal failure. This disease presents compensatory hypertrophy of the glomeruli and mesangial proliferation, administration of AM reduces the levels of proteinuria, suggesting that AM has an important modulator role in blood pressure and could be a therapeutic option for chronic renal failure.
Subject(s)
Humans , Adrenomedullin/physiology , Kidney/physiology , Adrenomedullin/therapeutic use , Kidney/physiopathology , Kidney Failure, Chronic/drug therapyABSTRACT
Background: Older females have less dynamic postural control and muscle strength than do middle-aged females. Aging-related strength losses may limit balancing performance. Objective: The purpose of this study was to investigate the ability of the Y Balance Test (YBT) and lower limb strength to discriminate between females in 2 age groups, the relationship between YBT distance and the Berg Balance Scale (BBS), and the degree to which performance on YBT distance is related to lower limb strength in middle-aged and older females. Method: The 40 healthy, independently active females were divided into 2 groups: older and middle-aged. The participants underwent measurements of YBT distance using the YBT, maximal muscular strength of the lower limbs using a handheld dynamometer, and the BBS. Results: The YBT distance in 3 directions and lower limb muscle strength for both lower limbs were significantly lower in the older adults than in the middle-aged group. A moderate correlation but insignificant correlation was found between the YBT composite distance and the BBS score. In the older females, YBT distance was significantly positively correlated with strength of the knee flexor and hip abductor. In the middle-aged group, YBT distance was significantly positively correlated with strength of the knee flexor and hip extensor. Conclusions: Performance on the YBT was influenced by the strength of lower limb. We suggested that YBT can be used to alternative as a measurement of dynamic balance. Proper training programs for older people could include not only strengthening exercises but also YBT performance to improve balance. .
Subject(s)
Animals , Female , Humans , Adrenomedullin/metabolism , Colorectal Neoplasms/genetics , Colorectal Neoplasms/metabolism , Proto-Oncogene Proteins/genetics , ras Proteins/genetics , Cell Line, Tumor , Cell Hypoxia/physiology , Immunohistochemistry , Mice, Nude , Oligonucleotide Array Sequence Analysis , Tumor Microenvironment/physiology , Xenograft Model Antitumor AssaysABSTRACT
<p><b>OBJECTIVE</b>To explore the predictive value of baseline plasma midregional fragment of pro-adrenomedullin level (MR-proADM) on long-term survival of postural tachycardia syndrome (POTS) children treated with midodrine hydrochloride.</p><p><b>METHODS</b>Fifty-three children (male 26, mean age (14.5 ± 4.5) years old) with POTS were included in this study, and all of them were diagnosed as POTS in our department from December 2007 to January 2010. Fifty-three children with POTS were divided into two groups according to the baseline plasma content of MR-proADM. Group I consisted of 35 POTS children with plasma content of MR-proADM > 61.5 ng/L, and the group II consisted of 18 POTS children with plasma content of MR-proADM ≤ 61.5 ng/L. The mean follow-up time was (67 ± 7) months. The orthostatic intolerance symptom score and the symptom free survival were compared between the 2 groups.</p><p><b>RESULTS</b>At the 60 months follow-up, the symptom score of children in group I was significantly lower than that in group II (χ(2) = 4.985, P < 0.05). At 72 months follow up, the symptom score was similar between the 2 groups (χ(2) = 0.004, P > 0.05) while the symptom free survival of group I was significantly higher than that in group II (χ(2) = 4.566, P < 0.05).</p><p><b>CONCLUSION</b>The baseline plasma MR-proADM level is value in predicting the long-term survival of POTS children treated with midodrine hydrochloride.</p>
Subject(s)
Adolescent , Child , Humans , Male , Adrenomedullin , Midodrine , Therapeutic Uses , Postural Orthostatic Tachycardia Syndrome , Diagnosis , Drug Therapy , ROC Curve , Vasoconstrictor Agents , Therapeutic UsesABSTRACT
The increase of pronociceptive mediators in the dorsal root ganglia (DRG) and spinal dorsal horn is an important mechanism in the pathogenesis of inflammatory pain and opioid tolerance. Adrenomedullin (AM) belongs to calcitonin gene-related peptide (CGRP) family and has been recently demonstrated to be a pain-related peptide. It has also been shown that the expression and release of AM are increased in the DRG and spinal dorsal horn during inflammation and repeated use of morphine. Intrathecal administration of the selective AM receptor antagonist AM22-52 abolishes inflammatory pain and morphine tolerance, suggesting that enhanced AM receptor signaling in the DRG and spinal dorsal horn contributes to the induction of inflammatory pain and morphine tolerance. The present review highlights the recent developments regarding the involvement of AM in these two disorders. The neurological mechanisms of AM's actions are also discussed.
Subject(s)
Animals , Rats , Adrenomedullin , Pharmacology , Calcitonin Gene-Related Peptide , Drug Tolerance , Ganglia, Spinal , Inflammation , Drug Therapy , Metabolism , Morphine , Pharmacology , Pain , Drug Therapy , Metabolism , Peptide Fragments , Pharmacology , Rats, Sprague-Dawley , Receptors, Adrenomedullin , MetabolismABSTRACT
<p><b>OBJECTIVE</b>Endogenous hydrogen sulfide (H2S), a novel gasotransmitter in cardiovascular regulation, plays an important protective role in the development and progression of atherosclerosis (AS). This study was designed to explore the effects of H2S donor on the production of adrenomedullin (ADM) and atrial natriuretic peptide (ANP) in AS rats.</p><p><b>METHODS</b>Male Sprague-Dawley rats were randomly divided into control group (n=10), AS group (n=10), and AS+NaHS group (n=10). Rats in the AS and AS+NaHS groups were given 3-day intraperitoneal injections of vitamin D3 and 8-week high-fat diet to induce AS, and the rats in the AS+NaHS group were intraperitoneally injected with H2S donor NaHS. Oil red O staining was applied to detect changes in the areas of the atherosclerotic plaques in the aortic root and the coronary artery; sulfide-sensitive electrode method was used to measure the plasma concentration of H2S. ADM and ANP levels in plasma were determined by radioimmunoassay.</p><p><b>RESULTS</b>Compared with the control group, marked atherosclerotic plaques were observed in the aortic root and the coronary artery in AS rats. Moreover, plasma H2S level decreased significantly, ADM level increased, and ANP level decreased significantly in AS rats (P<0.01). However, after the treatment with H2S donor NaHS for 8 weeks, the above changes in AS rats were reversed, demonstrated by significantly reduced areas of the atherosclerotic plaques in both the aortic root and the coronary artery, significantly increased plasma H2S level, significantly decreased plasma ADM level, and significantly increased plasma ANP level (P<0.01).</p><p><b>CONCLUSIONS</b>H2S plays an important regulatory effect on vasoactive peptides ADM and ANP in AS rats.</p>
Subject(s)
Animals , Male , Rats , Adrenomedullin , Atherosclerosis , Metabolism , Pathology , Atrial Natriuretic Factor , Hydrogen Sulfide , Pharmacology , Rats, Sprague-DawleyABSTRACT
The aim of the present study was to determine the mechanisms underlying the relaxant effect of adrenomedullin (AM) in rat cavernosal smooth muscle (CSM) and the expression of AM system components in this tissue. Functional assays using standard muscle bath procedures were performed in CSM isolated from male Wistar rats. Protein and mRNA levels of pre-pro-AM, calcitonin receptor-like receptor (CRLR), and Subtypes 1, 2 and 3 of the receptor activity-modifying protein (RAMP) family were assessed by Western immunoblotting and quantitative real-time polymerase chain reaction, respectively. Nitrate and 6-keto-prostaglandin F1α (6-keto-PGF1α; a stable product of prostacyclin) levels were determined using commercially available kits. Protein and mRNA of AM, CRLR, and RAMP 1, -2, and -3 were detected in rat CSM. Immunohistochemical assays demonstrated that AM and CRLR were expressed in rat CSM. AM relaxed CSM strips in a concentration-dependent manner. AM22-52, a selective antagonist for AM receptors, reduced the relaxation induced by AM. Conversely, CGRP8-37, a selective antagonist for calcitonin gene-related peptide receptors, did not affect AM-induced relaxation. Preincubation of CSM strips with NG-nitro-L-arginine-methyl-ester (L-NAME, nitric oxide synthase inhibitor), 1H-(1,2,4)oxadiazolo[4,3-a]quinoxalin-1-one (ODQ, quanylyl cyclase inhibitor), Rp-8-Br-PET-cGMPS (cGMP-dependent protein kinase inhibitor), SC560 [5-(4-chlorophenyl)-1-(4-methoxyphenyl)-3-trifluoromethyl pyrazole, selective cyclooxygenase-1 inhibitor], and 4-aminopyridine (voltage-dependent K+ channel blocker) reduced AM-induced relaxation. On the other hand, 7-nitroindazole (selective neuronal nitric oxide synthase inhibitor), wortmannin (phosphatidylinositol 3-kinase inhibitor), H89 (protein kinase A inhibitor), SQ22536 [9-(tetrahydro-2-furanyl)-9H-purin-6-amine, adenylate cyclase inhibitor], glibenclamide (selective blocker of ATP-sensitive K+ channels), and apamin (Ca2+-activated channel blocker) did not affect AM-induced relaxation. AM increased nitrate levels and 6-keto-PGF1α in rat CSM. The major new contribution of this research is that it demonstrated expression of AM and its receptor in rat CSM. Moreover, we provided evidence that AM-induced relaxation in this tissue is mediated by AM receptors by a mechanism that involves the nitric oxide-cGMP pathway, a vasodilator prostanoid, and the opening of voltage-dependent K+ channels.
Subject(s)
Animals , Male , Adrenomedullin/pharmacology , Calcitonin Receptor-Like Protein/analysis , Muscle, Smooth/drug effects , Parasympatholytics/pharmacology , Penis/drug effects , Vasodilator Agents/pharmacology , /pharmacology , /analysis , Adrenomedullin/genetics , Adrenomedullin/metabolism , Blotting, Western , Calcitonin Receptor-Like Protein/antagonists & inhibitors , Cyclic GMP-Dependent Protein Kinases/antagonists & inhibitors , Cyclooxygenase Inhibitors/pharmacology , Dose-Response Relationship, Drug , Enzyme Inhibitors/pharmacology , Immunohistochemistry , Indazoles/pharmacology , Muscle Relaxation , Muscle, Smooth/metabolism , Nitric Oxide Synthase/antagonists & inhibitors , Nitric Oxide/analysis , Nitric Oxide/analogs & derivatives , Penis/metabolism , Potassium Channels, Voltage-Gated/metabolism , Rats, Wistar , Real-Time Polymerase Chain Reaction , RNA, Messenger/metabolism , Receptor Activity-Modifying Protein 1/genetics , Receptor Activity-Modifying Protein 1/metabolism , /metabolism , /genetics , /metabolism , Receptors, Calcitonin Gene-Related Peptide/metabolismABSTRACT
<p><b>OBJECTIVE</b>To investigate the effect of adrenomedullin (ADM) on renal arteriole remodeling and phosphorylation of extracellular signal-regulated protein kinases 1/2 (p-ERK1/2) in spontaneous hypertensive rats (SHR).</p><p><b>METHODS</b>Male SHR (4 weeks old) were randomized into hypertensive group (SHR) and ADM-treated group (ADM) to receive subcutaneous saline and ADM injections (daily dose of 1.0 nmol/kg, 5 days a week), respectively, with age-matched Wistar-Kyota (WKY) rats as the blank control. The systolic blood pressure (SBP) was measured at the end of each week, and histological changes of the renal arterioles were observed using HE and Weigert staining; the expression of P-ERK1/2 in the arterioles was detected with immunohistochemistry and Western blotting.</p><p><b>RESULTS</b>At 16 and 24 weeks of age, the rats in both SHR and ADM groups showed significantly higher SBP levels than WKY rats (P<0.05), and at 24 weeks, SBP was significantly lower in ADM group than in SHR group (P<0.05). The intima thickness/lumen diameter (IT/LD) ratio of the renal arterioles increased in both SHR and ADM groups at 16 and 24 weeks as compared with that of WKY rats (P<0.05), and for arterioles with an outer diameter <40 µm, the IT/LD ratio was significantly lower at 24 weeks in ADM group than in SHR group (P<0.05). The renal expression of p-ERK1/2, which increased significantly in SHR and ADM groups at 16 and 24 weeks (P<0.05), was significantly lower in ADM group than in SHR group at 24 weeks (P<0.05).</p><p><b>CONCLUSIONS</b>Long-term ADM treatment can control SPB elevation in SHR rats and reduce renal arteriole remodeling by inhibiting the phosphorylation of ERK1/2.</p>
Subject(s)
Animals , Male , Rats , Adrenomedullin , Pharmacology , Arterioles , Blood Pressure , Hypertension , Kidney , Mitogen-Activated Protein Kinase 1 , Metabolism , Mitogen-Activated Protein Kinase 3 , Metabolism , Rats, Inbred SHR , Rats, Wistar , Vascular RemodelingABSTRACT
<p><b>OBJECTIVE</b>To observe the vasodilating effect of adrenomedullin 2 (ADM2) by antagonizing angiotensin 1 (Ang II), and to explore its mechanism.</p><p><b>METHODS</b>Eighteen male, 180-200 g SD rats were randomly divided into 3 groups (n = 6): control group, Ang II (150 ng/(kg x min)) group and Ang II (150 ng/(kg x min)) + ADM2(500 ng/(kg x h)) group. Mini-osmotic pumps filled with peptide were implanted in the back of rats subcutaneously. After two weeks, the blood pressure was measured by the way of carotid intubation. The plasma was collected for the detection of nitric oxide (NO) content and the activity of endothelial nitric oxide synthase (eNOS). The in situ oxidation of fluorescent dye dihydroethidium (DHE) was used for detecting superoxide in rat arteries. The rat isolated arterial rings were made for studying the vasodilating effect of ADM2. Human umbilical vein endothelial cell line EA. hy 926 cells were cultured and their intracellular reactive oxygen species (ROS) were evaluated by probe DCFH-DA.</p><p><b>RESULTS</b>ADM2 dramatically decreased the blood pressure in angiotensin II-induced hypertension rat model, enhanced plasma NO content and the activity of eNOS and reduced superoxide formation in vessel walls. ADM2 also induced relaxation of the vascular rings preconstricted by Ang II in a concentration-dependent and endothelium-dependent manner. In cultured vascular endothelium, ADM2 ameliorated the ROS generation induced by Ang II.</p><p><b>CONCLUSION</b>Adrenomedullin 2 relaxed blood vessels by antagonizing angiotensin II-induced oxidative stress and improving the vascular endothelial function.</p>
Subject(s)
Animals , Humans , Male , Rats , Adrenomedullin , Pharmacology , Angiotensin II , Pharmacology , Antihypertensive Agents , Pharmacology , Blood Pressure , Drug Antagonism , Endothelium, Vascular , Human Umbilical Vein Endothelial Cells , Cell Biology , Nitric Oxide , Blood , Nitric Oxide Synthase Type III , Blood , Oxidative Stress , Rats, Sprague-Dawley , Reactive Oxygen Species , Metabolism , VasodilationABSTRACT
OBJECTIVES: Administering steroids before cardiopulmonary bypass in pediatric heart surgery modulates systemic inflammatory response syndrome and improves postoperative recovery. However, the use of steroids aggravates hyperglycemia, which is associated with a poor prognosis. Adult patients with systemic inflammatory response syndrome usually evolve with hyperglycemia and high insulin levels, whereas >90% of pediatric patients exhibit hyperglycemia and low insulin levels. This study aims to determine: A) the metabolic and inflammatory factors that are associated with hyperglycemia and low insulin levels in children who underwent cardiac surgery with cardiopulmonary bypass and who received a single high dose of methylprednisolone and B) the best predictors of insulin variation using a mathematical model. METHODS: This preliminary study recruited 20 children who underwent heart surgery with cardiopulmonary bypass and received methylprednisolone (30 mg/kg) immediately after anesthesia. Among the 20 patients initially recruited, one was excluded because of the absence of hyperglycemia and lower insulin levels after surgery. However, these abnormalities were confirmed in the remaining 19 children. The C-peptide, CRP, IL-6, and adrenomedullin levels were measured before surgery, immediately after cardiopulmonary bypass, and on the first, second, and third days after cardiac surgery. RESULTS: IL-6, CRP, and adrenomedullin increments were observed, whereas the C-peptide levels remained within reference intervals. CONCLUSION: The multiple regression model demonstrated that in addition to age and glycemia (two well-known factors that are directly involved in glucose metabolism), adrenomedullin and IL-6 levels were independent factors associated with lower insulin concentrations. These four parameters were responsible for 64.7% of the observed insulin variances. In addition, the fact that C-peptide levels did not fall together with insulin could have grounded the medical decision not to administer insulin to patients.
Subject(s)
Child, Preschool , Female , Humans , Infant , Male , Anti-Inflammatory Agents/adverse effects , Cardiac Surgical Procedures/methods , Cardiopulmonary Bypass/methods , Hyperglycemia/chemically induced , Insulin/blood , Methylprednisolone/adverse effects , Age Factors , Adrenomedullin/blood , Anti-Inflammatory Agents/administration & dosage , Blood Glucose/analysis , Blood Glucose/drug effects , C-Peptide/blood , C-Reactive Protein/analysis , Insulin/deficiency , /blood , Models, Biological , Methylprednisolone/administration & dosage , Postoperative Period , Reference Values , Regression AnalysisABSTRACT
The calcitonin gene-related peptide (CGRP) family mainly includes CGRPα, CGRPβ, adrenomedullin, calcitonin and amylin. The members of CGRP family and their receptors are widely distributed in the central and peripheral nervous systems. Studies show that members of CGRP family such as CGRP and adrenomedullin play important roles in the transmission of nociceptive information. At spinal level, CGRP promotes the transmission of nociceptive information, spinal morphine tolerance, migraine, inflammatory pain and neuropathic pain. At superspinal level, CGRP suppresses the transmission of nociceptive information. Adrenomedullin is a pain-related neuropeptide which has recently been demonstrated. It facilitates the transmission of nociceptive information and is involved in the development and maintenance of opioid tolerance. The involvement of amylin and calcitonin in pain is not clear yet.
Subject(s)
Animals , Humans , Adrenomedullin , Physiology , Analgesics, Opioid , Pharmacology , Calcitonin Gene-Related Peptide , Physiology , Drug Tolerance , Islet Amyloid Polypeptide , Physiology , Nociception , PainABSTRACT
La adrenomedulina (AM) es un péptido ubicuo de 52 residuos de aminoácidos que cumple funciones importantes en la regulación de la función cardiovascular (CDV). La AM ejerce sus acciones a través de su unión con tres subtipos de receptores, el receptor del péptido relacionado al gen de la calcitonina tipo 1 (CGRP1), el receptor de AM tipo 1 (AM1) y tipo 2 (AM2). El CGRP1 está formado por el receptor similar al receptor de calcitonina (CRLR) y la proteína que modifica la actividad del receptor tipo 1 (RAMP1). El AM1 por el CRLR+RAMP2 y el AM2 por el CRLR+RAMP3. A nivel del sistema nervioso central, la AM y sus receptores se localizan en diversas regiones, incluyendo el cerebelo. Se ha demostrado marcados incrementos en la densidad de los sitios de unión para la AM en el cerebelo durante la hipertensión, lo que sugiere un papel del sistema adrenomedulinérgico cerebeloso en la regulación de la presión arterial (PA). En el presente estudio se evaluó la participación de la AM cerebelosa en la regulación de la PA. Nuestros hallazgos muestran la existencia de desregulación de los componentes del sistema AM cerebeloso durante la hipertensión, ya que se encontró una reducida expresión de CRLR, RAMP1 y RAMP3 y una incrementada expresión de la AM y RAMP2 en el vermis de cerebelo de ratas hipertensas (SHR), cuando se comparó con las ratas controles, Wistar Kyoto (WKY), de 8 y 16 semanas de edad. La reducción de la PA mediante el tratamiento crónico con valsartán (60mg/Kg/día,p.o.) revirtió las desregulación de la AM y los componentes de su receptor, observados en las ratas SHR. El papel de las especies reactivas de oxígeno (EROS) en la acción de la AM cerebelosa quedó evidenciado, ya que la AM fue capaz de reducir la actividad de las tres enzimas antioxidantes, superóxiodo dismutasa (SOD), catalasa (CAT) y glutatión peroxidasa (GPx), en las ratas WKY y Sprague - Dawley (SD). Aún mas, nuestros hallazgos mostraron claramente el efecto antagónico entre la AM y la ANG II sobre la actividad de las enzimas antioxidantes inducida por la ANG II. El efecto de la AM sobre las enzimas antioxidantes no se manifestó en la ratas hipertensas, sin embargo el mismo fue restaurado mediante la disminución de la presión arterial con la administración crónica de dos antihipertensivos de mecanismo de acción distintos como la amlodipina (5mg/Kg/día,p.o) o el valsartán (60mg/Kg/día,p.o), lo que sugiere una relación entre la hipertensión y ausencia del efecto de AM en la ratas SHR. Al evaluar la posible vía de señalización que media la acción de la AM y el antagonismo con la ANG II sobre la actividad de las enzimas antioxidantes, demostramos que no existe una vía final común para dicho antagonismo, siendo la proteína quinasa A (PKA) y los 3 subtipos de receptores CGRP1, AM1 y AM2 los que median la acción de la AM, mientras que la acción de la ANG II se encuentra mediada a través de una vía que involucra la PKC/NAD(P)H oxidasa. Los hallazgos demuestran el antagonismo entre la AM y la ANG II en la regulación del estrés oxidativo en el cerebelo y ratifican la desregulación de la señalización de la AM mediada por EROs durante la hipertensión. Al evaluar las vías de señalización intracelular que median la acción de la AM en el cerebelo, demostramos que la AM es capaz de activar a las ERK, la producción de GMPc y NO a través de la estimulación del receptor AM1, y del AMPc a través de los tres subtipos de receptores de AM, lo que apoya que en el cerebelo la AM ejerce acciones a través de diversas vías de señalización como lo son NO/GMPc, AC/AMPc/PKA y/o ERK. El posible papel funcional de la AM in vivo fue inequívoco, ya que se demostró que la microinyección de AM en el vermis cerebeloso produjo una respuesta hipotensora profunda en las ratas SHR pero no en las normotensas. El hecho que la microinyección de AM en el vermis cerebelar en las ratas SD, WKY y SHR disminuyó significativamente la respuesta presora frente al estrés simpatoadrenal inducido por el estímulo eléctrico plantar, sugiere que la acción hipotensora está mediada a través de la regulación del eflujo simpático e indica un posible papel de la AM en la regulación de la respuesta CDV frente al estrés. En conjunto, nuestros resultados demuestran la existencia de un sistema adrenomedulinérgico funcional en el cerebelo, e indican por primera vez, que la AM cumple un papel importante en la regulación de la PA durante la hipertensión y el estrés.
Subject(s)
Animals , Male , Rats , Adrenomedullin/metabolism , Arterial Pressure/physiology , Cerebellar Vermis/metabolism , Hypertension/metabolism , Rats, Inbred SHR , Rats, Inbred WKY , Time Factors , Vasoconstrictor Agents/administration & dosage , Angiotensin II/administration & dosage , Blotting, Western , Rats, Sprague-Dawley , Amlodipine/administration & dosage , Oxidative Stress , Models, Animal , Adrenomedullin/administration & dosage , Receptors, Adrenomedullin/metabolism , Arterial Pressure/drug effects , Cerebellar Vermis/drug effects , Cerebellar Vermis/enzymology , Valsartan/administration & dosage , Antihypertensive Agents/administration & dosageABSTRACT
Our objective was to investigate in conscious Sprague-Dawley (6-8 weeks, 250-300 g) female rats (N = 7 in each group) the effects of intracerebroventricularly (icv) injected adrenomedullin (ADM) on blood pressure and heart rate (HR), and to determine if ADM and calcitonin gene-related peptide (CGRP) receptors, peripheral V1 receptors or the central cholinergic system play roles in these cardiovascular effects. Blood pressure and HR were observed before and for 30 min following drug injections. The following results were obtained: 1) icv ADM (750 ng/10 µL) caused an increase in both blood pressure and HR (DMAP = 11.8 ± 2.3 mmHg and ΔHR = 39.7 ± 4.8 bpm). 2) Pretreatment with a CGRP receptor antagonist (CGRP8-37) and ADM receptor antagonist (ADM22-52) blocked the effect of central ADM on blood pressure and HR. 3) The nicotinic receptor antagonist mecamylamine (25 µg/10 µL, icv) and the muscarinic receptor antagonist atropine (5 µg/10 µL, icv) prevented the stimulating effect of ADM on blood pressure. The effect of ADM on HR was blocked only by atropine (5 µg/10 µL, icv). 4) The V1 receptor antagonist [β-mercapto-β-β-cyclopentamethylenepropionyl¹, O-me-Tyr²,Arg8]-vasopressin (V2255; 10 µg/kg), that was applied intravenously, prevented the effect of ADM on blood pressure and HR. This is the first study reporting the role of specific ADM and CGRP receptors, especially the role of nicotinic and muscarinic central cholinergic receptors and the role of peripheral V1 receptors in the increasing effects of icv ADM on blood pressure and HR.
Subject(s)
Animals , Female , Rats , Adrenomedullin/pharmacology , Blood Pressure/drug effects , Cholinergic Neurons/physiology , Heart Rate/drug effects , Vasodilator Agents/pharmacology , Vasopressins/drug effects , Adrenomedullin/administration & dosage , Central Nervous System/drug effects , Central Nervous System/physiology , Cholinergic Neurons/drug effects , Consciousness/drug effects , Consciousness/physiology , Injections, Intraventricular , Rats, Sprague-Dawley , Receptors, Calcitonin Gene-Related Peptide/drug effects , Receptors, Calcitonin Gene-Related Peptide/physiology , Vasodilator Agents/administration & dosage , Vasopressins/physiologyABSTRACT
<p><b>OBJECTIVE</b>To observe the effect of adrenomedullin (ADM) on the pulmonary vascular collagen metabolism in hypoxic rats in order to study the effect of ADM on chronic hypoxic pulmonary vascular structural remodeling and its possible mechanism.</p><p><b>METHODS</b>Nineteen male Wistar rats were randomly divided into three groups: normal control (n=6), hypoxia (n=7) and ADM-treated hypoxia (n=6). ADM was subcutaneously administered into rats of the ADM-treated hypoxia group by mini-osmotic pump (300 ng/h) for two weeks. After two weeks of hypoxic challenge, mean pulmonary arterial pressure (mPAP) was evaluated using a right cardiac catheterization procedure. The ratio of right ventricular mass to left ventricular plus septal mass[RV/ (LV+S)] was measured. The changes of pulmonary vascular microstructure were observed. Meanwhile, the expression levels of collagen I, collagen III and transforming growth factor (TGF)-β in pulmonary arteries were detected by immunohistochemical assay.</p><p><b>RESULTS</b>mPAP and RV/(LV+S) increased significantly in the hypoxia group compared with normal controls (P<0.01). The muscularization of small pulmonary vessels and the relative medial thickness of pulmonary arteries increased obviously in the hypoxia group compared with those in the normal control group (P<0.01). Meanwhile, the expression levels of collagen I, collagen III and TGF-β of pulmonary arteries in the hypoxia group increased markedly compared with those in the normal control group. However, mPAP and RV/(LV+S) were significantly reduced in the ADM-treated hypoxia group compared with those in the hypoxia group (P<0.01). ADM ameliorated pulmonary vascular structural remodeling of hypoxic rats, with a decrease in the expression of collagen I, collagen III and TGF-β of pulmonary arteries.</p><p><b>CONCLUSIONS</b>ADM might play a regulatory role in the development of hypoxic pulmonary hypertension and hypoxic pulmonary vascular remodeling, through inhibiting the expression of TGF-β and alleviating the collagen accumulation of pulmonary arteries.</p>
Subject(s)
Animals , Male , Rats , Adrenomedullin , Pharmacology , Collagen , Metabolism , Hypertension, Pulmonary , Metabolism , Hypoxia , Pulmonary Artery , Metabolism , Rats, Wistar , Transforming Growth Factor beta , PhysiologyABSTRACT
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.
Subject(s)
Animals , Male , Rats , Adrenomedullin/pharmacology , Apoptosis/drug effects , Calcitonin Receptor-Like Protein/metabolism , Cardiotonic Agents/pharmacology , Cyclic AMP/metabolism , Disease Models, Animal , L-Lactate Dehydrogenase/metabolism , Malondialdehyde/metabolism , Myocardial Ischemia/pathology , Myocardium/pathology , Neuropeptides/pharmacology , Proto-Oncogene Proteins c-bcl-2/metabolism , RNA, Messenger/metabolism , Random Allocation , Rats, Sprague-Dawley , Real-Time Polymerase Chain Reaction , Receptor Activity-Modifying Proteins/metabolism , Superoxide Dismutase/metabolismABSTRACT
<p><b>OBJECTIVE</b>To observe the effects of exogenous adrenomedullin (ADM) on endogenous expression of ADM in the kidney and hypothalamus of rats early after mechanical renal trauma.</p><p><b>METHODS</b>Adult Wistar rats were randomized into 4 groups (n=32), namely the control group, renal impact trauma group, preventive ADM injection group, and therapeutic ADM injection group. In the latter two groups, ADM (0.1 nmol/kg) was administrated by intraperitoneal injection 10 min before and 10 min after renal trauma. The rats were executed at 1, 6, 12, and 24 h after the trauma to examine the expression of ADM in the kidney and hypothalamus.</p><p><b>RESULTS</b>In preventive ADM injection group, the renal expression of ADM increased significantly at 1 h after the trauma (P<0.05) and tended to further increase with time till 24 h when its expression recovered the normal level. In the therapeutic ADM injection group, strong renal ADM positivity was found at 1 and 6 h after the injury (P<0.05) followed by gradual decrease till recovering the normal level at 24 h. Low renal ADM expression was detected, which was the strongest at 1 and 12 h (P<0.05) and became normal at 24 h. The time course of ADM expression in the hypothalamus was similar to that in the kidney in the therapeutic ADM injection group, and in the preventive injection group, the strongest ADM expression in the hypothalamus occurred at 6 and 24 h, and the lowest expression occurred at 12 h (P<0.05). The trauma group showed significantly decreased ADM expression in the hypothalamus compared with the control group (P<0.05).</p><p><b>CONCLUSION</b>The hypothalamic ADM expression can upregulate renal ADM expression. ADM maintains the relative stability of the internal environment and physiological activity by local and systemic positive and negative feedback mechanisms.</p>