RESUMO
Cardiac contractility increases as sarcomere length increases, suggesting that intrinsic molecular mechanisms underlie the Frank-Starling relationship to confer increased cardiac output with greater ventricular filling. The capacity of myosin to bind with actin and generate force in a muscle cell is Ca(2+) regulated by thin-filament proteins and spatially regulated by sarcomere length as thick-to-thin filament overlap varies. One mechanism underlying greater cardiac contractility as sarcomere length increases could involve longer myosin attachment time (ton) due to slowed myosin kinetics at longer sarcomere length. To test this idea, we used stochastic length-perturbation analysis in skinned rat papillary muscle strips to measure ton as [MgATP] varied (0.05-5 mM) at 1.9 and 2.2 µm sarcomere lengths. From this ton-MgATP relationship, we calculated cross-bridge MgADP release rate and MgATP binding rates. As MgATP increased, ton decreased for both sarcomere lengths, but ton was roughly 70% longer for 2.2 vs. 1.9 µm sarcomere length at maximally activated conditions. These ton differences were driven by a slower MgADP release rate at 2.2 µm sarcomere length (41 ± 3 vs. 74 ± 7 s(-1)), since MgATP binding rate was not different between the two sarcomere lengths. At submaximal activation levels near the pCa50 value of the tension-pCa relationship for each sarcomere length, length-dependent increases in ton were roughly 15% longer for 2.2 vs. 1.9 µm sarcomere length. These changes in cross-bridge kinetics could amplify cooperative cross-bridge contributions to force production and thin-filament activation at longer sarcomere length and suggest that length-dependent changes in myosin MgADP release rate may contribute to the Frank-Starling relationship in the heart.
Assuntos
Difosfato de Adenosina/metabolismo , Miocárdio/metabolismo , Miosinas/metabolismo , Sarcômeros/fisiologia , Sarcômeros/ultraestrutura , Actinas/metabolismo , Animais , Cálcio/farmacologia , Elasticidade , Técnicas In Vitro , Cinética , Masculino , Contração Miocárdica/efeitos dos fármacos , Contração Miocárdica/fisiologia , Músculos Papilares/metabolismo , Músculos Papilares/ultraestrutura , Ratos , Ratos Sprague-Dawley , Processos Estocásticos , ViscosidadeRESUMO
Se realizó un estudio descriptivo de las características anatómicas y biométricas del músculo papilar septal en 30 corazones de individuos adultos chilenos, en edades comprendidas entre 18 y 84 años de edad, de ambos sexos, sin aparente patología cardíaca, pertenecientes a la Unidad de Anatomía Humana Normal del Departamento de Ciencias Básicas de la Universidad de La Frontera. Los resultados mostraron que el músculo papilar septal, se presenta en un 83,3 por ciento de los corazones del estudio. De éstos, el 44,0 por ciento presenta un solo músculo, el 28 por ciento presenta dos músculos y el 28 por ciento tres músculos papilares septales. De los músculos papilares septales encontrados, el 71,1 por ciento correspondió a la forma cono libre, el 24,4 por ciento a la forma cono pegado y el 4,5 por ciento a la forma puente. En cuanto a la longitud de forma cono pegado y cono libre, el rango que se encuentra en mayor porcentaje está entre 4,0 mm 5,99 mm; con un 45,5 por ciento y 42,4 por ciento, respectivamente. Este estudio nos demuestra la importancia de incorporar al músculo papilar septal a la nomenclatura anatómica internacional.
A descriptive research study was carried out on the anatomical and biometric characteristics of the septal papillary muscle in 30 hearts of adult Chilean subjects, between 18 and 84 years of age of both sexes and without apparent cardiac pathology, from the Normal Human Anatomy Unit, Basic Sciences Department of the Universidad de La Frontera. Results show that the septal papillary muscle was present in 83.3 percent of the hearts in the study. Of these 44.0 percent show one muscle only, 28 percent show two muscles and 28 percent show three septal papillary muscles. In the septal papillary muscles found, 71.1 percent are free cone-shaped, 24.4 percent were attached cone-shaped, and 4.5 percent were bridge-shaped. Regarding the length of attached cone and free cone shaped, the highest percentage range was between 4.0 mm and 5.99 mm, with 45.5 percent and 42.4 percent respectively. The present study shows the importance of integrating the septal papillary muscle to the International Anatomical Nomenclature.
Assuntos
Idoso , Músculos Papilares/anatomia & histologia , Músculos Papilares/ultraestrutura , Septos Cardíacos/anatomia & histologia , Septos Cardíacos/embriologia , Septos Cardíacos/ultraestrutura , Anatomia Regional/métodos , ChileRESUMO
FUNDAMENTO: Os efeitos do envelhecimento no músculo papilar têm sido amplamente demonstrados, mas não há dados disponíveis sobre os efeitos do exercício nas alterações relacionadas à idade. OBJETIVO: Analisar os efeitos do envelhecimento nas propriedades morfológicas e quantitativas do músculo papilar e investigar se um programa contínuo de exercícios moderados pode exercer um efeito protetor contra as conseqüências do envelhecimento. MÉTODOS: Microscopia eletrônica foi utilizada para estudar a densidade dos miócitos, capilares e tecido conectivo e área transversal dos miócitos do músculo papilar no ventrículo esquerdo de ratos Wistar de 6 e 13 meses, não-treinados e submetidos a exercícios. RESULTADOS: Como esperado, a densidade de volume dos miócitos diminui significantemente (p<0,05) com a idade. A densidade de comprimento dos capilares também diminui com a idade, mas não de forma significante. A fração de volume intersticial do tecido do músculo capilar aumenta significantemente com a idade (P<0,05). O número de perfis de miócitos mostrou uma redução de 20% que foi acompanhada de hipertrofia dos miócitos no envelhecimento (P<0,05). Animais submetidos a uma sessão diária de 60 minutos, 5 dias/semana a 1,8 km.h-1 de corrida moderada em esteira ergométrica durante 28 semanas mostraram uma reversão de todos os efeitos do envelhecimento observados no músculo papilar. CONCLUSÃO: O presente estudo apóia o conceito de que treinamento físico de longo prazo impede as mudanças deletérias relacionadas à idade no músculo capilar.
BACKGROUND: The effects of aging on papillary muscle have been widely demonstrated, but no data on the effects of exercise on the age-related changes are available. OBJECTIVE: To analyze the effects of aging on the morphological and quantitative properties of papillary muscle and investigate whether a long-term moderate exercise program would exert a protective effect against the effects of aging. METHODS: We used electron microscopy to study the density of myocytes, capillaries and connective tissue and the cross-sectional area of myocytes of the papillary muscle of the left ventricle of 6- and 13-month-old untrained and exercised Wistar rats. RESULTS: As expected, the volume density of myocytes declined significantly (p<0.05) with aging. The length density of myocardial capillaries also declined with aging, but not significantly. The interstitial volume fraction of the papillary muscle tissue increased significantly (P<0.05) with age. The number of myocyte profiles showed a reduction of 20% that was accompanied by myocyte hypertrophy in the aged rats (P<0.05). Animals submitted to a 60-minute daily session,, 5 days/wk at 1.8 km.h-1 of moderate running on a treadmill for 28 weeks showed a reversion of all the observed aging effects on papillary muscle. CONCLUSION: The present study supports the concept that long-term exercise training restrains the aging-related deleterious changes in the papillary muscle.
FUNDAMENTO: Los efectos del envejecimiento en el músculo papilar han sido demostrados de modo amplio, pero no hay datos disponibles sobre los efectos del ejercicio en las alteraciones relacionadas a la edad. OBJETIVO: Analizar los efectos del envejecimiento en las propiedades morfológicas y cuantitativas del músculo papilar e investigar si un programa continuo de ejercicios moderados puede ejercer un efecto protector contra las consecuencias del envejecimiento. MÉTODOS: Se utilizó microscopia electrónica para estudiar la densidad de los miocitos, capilares y tejido conectivo, así como el área transversal de los miocitos del músculo papilar en el ventrículo izquierdo de ratas Wistar de 6 y 13 meses, no entrenadas y sometidas a ejercicios. RESULTADOS: Como se esperaba, la densidad de volumen de los miocitos disminuye significantemente (p<0,05) con el avance de la edad. La densidad de longitud de los capilares también disminuye con la edad, pero no de forma significante. La fracción de volumen intersticial del tejido del músculo capilar aumenta significantemente con el avance de la edad (P<0,05). El número de perfiles de miocitos mostró una reducción del 20%, seguida de su hipertrofia en el envejecimiento (P<0,05). Sometidos a una sesión diaria de 60 minutos, 5 días/semana a 1,8 km.h-1 de corrida moderada en estera ergométrica durante 28 semanas, los animales mostraron una reversión de todos los efectos del envejecimiento observados en el músculo papilar. CONCLUSIÓN: El presente estudio apoya el concepto de que entrenamiento físico de largo plazo impide los cambios letales en el músculo capilar relacionados a la edad.
Assuntos
Animais , Masculino , Ratos , Envelhecimento/metabolismo , Miócitos Cardíacos/fisiologia , Condicionamento Físico Animal , Músculos Papilares/fisiologia , Análise de Variância , Ventrículos do Coração/ultraestrutura , Miócitos Cardíacos/ultraestrutura , Músculos Papilares/ultraestrutura , Condicionamento Físico Animal/métodos , Ratos WistarRESUMO
Os tumores cardíacos primários do coração são raros, com uma prevalência entre 0,0017 por cento e 0,19 por cento dos estudos de autópsia não selecionados. Cerca de 75 por cento são tumores benignos e quase a metade são mixomas. Os restantes se dividem entre rabdomiomas, lipomas e fibroelastomas. Os mixomas são os tumores cardíacos mais comuns na idade adulta e os rabdomiomas, os mais comuns da população pediátrica. O fibroelastoma papilífero (FEP) é um tumor benigno do coração, relativamente raro, correspondendo a aproximadamente 8 por cento dos tumores cardíacos. São os que mais comumente acometem as valvas cardíacas . No passado, consistiam de achados de necropsia ou eram encontrados em procedimentos cirúrgicos ao acaso. O diagnóstico in vivo era esporádico². Com o aprimoramento das técnicas de ecocardiografia, o FEP tem sido diagnosticado com maior freqüência. São, geralmente, descritos como uma massa móvel, pedunculada, bem delimitada e com predileção pelo endocárdio valvar. A proposta terapêutica, quando pedunculados, é a ressecção cirúrgica, visando a prevenção de fenômenos embólicos cerebrais, pulmonares, coronarianos ou periféricos1,3. Serão apresentados cinco casos diagnosticados em nossa instituição, no período de agosto de 1995 a junho de 2004.
Assuntos
Adulto , Pessoa de Meia-Idade , Humanos , Masculino , Feminino , Fibroma/patologia , Neoplasias Cardíacas/patologia , Músculos Papilares/patologia , Autopsia , Fibroma , Fibroma/ultraestrutura , Neoplasias Cardíacas , Neoplasias Cardíacas/ultraestrutura , Imageamento por Ressonância Magnética , Músculos Papilares , Músculos Papilares/ultraestruturaRESUMO
BACKGROUND: Synchrotron radiation has been used to analyze crossbridge dynamics in isolated papillary muscle and excised perfused hearts with the use of x-ray diffraction techniques. We showed that these techniques can detect regional changes in rat left ventricle contractility and myosin lattice spacing in in situ ejecting hearts in real time. Furthermore, we examined the sensitivity of these indexes to regional ischemia. METHODS AND RESULTS: The left ventricular free wall of spontaneously beating rat hearts (heart rate, 290 to 404 bpm) was directly exposed to brief high-flux, low-emittance x-ray beams provided at SPring-8. Myosin mass transfer to actin filaments was determined as the decrease in reflection intensity ratio (intensity of 1,0 plane over the 1,1 plane) between end-diastole and end-systole. The distance between 1,0 reflections was converted to a lattice spacing between myosin filaments. We found that mass transfer (mean, 1.71+/-0.09 SEM, n=13 hearts) preceded significant increases in lattice spacing (2 to 5 nm) during systole in nonischemic pericardium. Left coronary occlusion eliminated increases in lattice spacing and severely reduced mass transfer (P<0.01) in the ischemic region. CONCLUSIONS: Our results suggest that x-ray diffraction techniques permit real-time in situ analysis of regional crossbridge dynamics at molecular and fiber levels that might also facilitate investigations of ventricular output regulation by the Frank-Starling mechanism.
Assuntos
Miocárdio/química , Miosinas/química , Difração de Raios X , Citoesqueleto de Actina/química , Citoesqueleto de Actina/ultraestrutura , Actomiosina/química , Actomiosina/ultraestrutura , Animais , Sistemas Computacionais , Coração/efeitos da radiação , Ventrículos do Coração/química , Masculino , Contração Miocárdica , Isquemia Miocárdica/metabolismo , Isquemia Miocárdica/fisiopatologia , Miocárdio/ultraestrutura , Miosinas/ultraestrutura , Músculos Papilares/química , Músculos Papilares/ultraestrutura , Conformação Proteica , Ratos , Ratos Sprague-Dawley , Sarcômeros/química , Sarcômeros/ultraestrutura , Síncrotrons , Função VentricularRESUMO
We examined the sarcomere length-dependence of the spacing of the hexagonal lattice of the myofilaments and the mass transfer of myosin cross-bridges during contraction of right ventricular papillary muscle of the rat. The lattice spacing and mass transfer were measured by using X-ray diffraction, and the sarcomere length was monitored by laser diffraction at the same time. Although the lattice spacing and the sarcomere length were inversely related, their relationship was not exactly isovolumic. The cell volume decreased by about 15% when the sarcomere length was shortened from 2.3 micro m to 1.8 micro m. Twitch tension increased with sarcomere length (the Frank-Starling law). At the peak tension, the ratio of the intensity of the (1,0) equatorial reflection to that of the (1,1) reflection was smaller when the tension was greater, showing that the larger tension at a longer sarcomere length accompanies a larger amount of mass transfer of cross-bridges from the thick to the thin filament. The result suggests that the Frank-Starling law is due to an increase in the number of myosin heads attached to actin, not in the average force produced by each head.
Assuntos
Coração/fisiologia , Miocárdio/ultraestrutura , Miosinas/fisiologia , Sarcômeros/fisiologia , Sarcômeros/ultraestrutura , Animais , Fenômenos Biofísicos , Biofísica , Técnicas In Vitro , Masculino , Microscopia Confocal , Contração Miocárdica/efeitos dos fármacos , Músculos Papilares/fisiologia , Músculos Papilares/ultraestrutura , Ratos , Ratos Wistar , Difração de Raios XRESUMO
OBJECTIVE: The primary aim of this study was to investigate whether activation of Na influx via voltage-gated Na channels can elevate sub-sarcolemmal ('fuzzy-space') [Na] and transiently activate Na/K pump current (I(p)). METHODS AND RESULTS: Initially, Na/K pump activity was characterised in whole-cell voltage-clamped single guinea-pig ventricular myocytes. I(p) was activated by intracellular Na with a K(m) of 15.5 mM and a Hill coefficient of 1.7. Extracellular K activated I(p) with a K(m) of 1.6 mM. In these experiments, a finite ouabain-sensitive I(p) was measured when the pipette [Na] was zero. This suggests that there is an accumulation of Na in a sub-sarcolemmal space that is not in equilibrium with the bulk cytosol (which is assumed to be efficiently dialysed by the low-resistance patch-pipettes used). Such a sub-sarcolemmal Na gradient was observed in separate experiments in intact rabbit papillary muscles using electron probe X-ray microanalysis. In these studies, a fuzzy-space of limited Na diffusion was observed 100-200 nm below the sarcolemmal membrane. This sub-sarcolemmal Na gradient was similar whether muscles were frozen at peak-systole or end-diastole suggesting that the fuzzy-space Na does not change over the course of the contractile cycle. This was further investigated in isolated guinea pig myocytes where evidence for a transient activation of I(p) was sought immediately after the activation of voltage-gated Na channels. A single clamp step from -80 to 0 mV activated Na influx but, in the 10-2000 ms immediately following the initial Na influx no evidence for a transient activation of I(p) was observed. Similarly, no activation of I(p) could be detected immediately following a train of 20 rapid (5-Hz) pulses designed to maximise Na influx. CONCLUSIONS: These studies provide evidence for the existence of a maintained sub-sarcolemmal elevation of [Na] in ventricular myocardium; however, this fuzzy-space [Na] did not change immediately after the activation of Na influx via voltage-gated Na channels or throughout the contractile cycle.
Assuntos
Miocárdio/metabolismo , Sarcolema/metabolismo , ATPase Trocadora de Sódio-Potássio/metabolismo , Sódio/metabolismo , Animais , Microanálise por Sonda Eletrônica , Cobaias , Ventrículos do Coração/citologia , Ventrículos do Coração/metabolismo , Masculino , Miócitos Cardíacos/metabolismo , Músculos Papilares/ultraestrutura , Técnicas de Patch-Clamp , Coelhos , Canais de Sódio/fisiologiaRESUMO
Endothelin-1 (ET-1) induces severe pathologic conditions such as coronary spasm followed by vasospastic angina pectoris and acute myocardial infarction. The related pathophysiologic mechanisms have remained obscure. Endothelin-1 receptor (ET(A) and ET(B)) is reported to couple with several types of G protein-involved pathways that participate in phospholipase C activation and atrial myofibrils organization into sarcomeric units. Here we demonstrate that ET-1 induces histologic and pathologic dysfunction in the rabbit myocardium and that such pathologic events are prevented by the Rho-kinase inhibitor fasudil. Although the bolus injection of ET-1 (1.4 nmol/kg) via the auricular vein of the rabbit induced only transient T-wave elevation, irreversible, severe histologic changes were observed in papillary muscles of the ventricle, and multifocal myocardial necrosis with infiltration of neutrophils and macrophages in the left ventricle occurred. Oral administration of fasudil (10 mg/kg) significantly reduced the occurrence of myocardial injury determinants, whereas conventional Ca2+ channel blockers (nifedipine, diltiazem) and a K+ channel opener (nicorandil; 10 mg/kg, p.o. each) showed a lesser or no effect on such determinants. These results suggest that ET-1 induces severe myocardial dysfunction based not only on the occurrence of vasospastic ischemia but also on its direct effects on the myocardium.
Assuntos
1-(5-Isoquinolinasulfonil)-2-Metilpiperazina/análogos & derivados , Endotelina-1/antagonistas & inibidores , Inibidores Enzimáticos/uso terapêutico , Isquemia Miocárdica/prevenção & controle , Músculos Papilares/efeitos dos fármacos , 1-(5-Isoquinolinasulfonil)-2-Metilpiperazina/farmacologia , Animais , Movimento Celular/efeitos dos fármacos , Diltiazem/farmacologia , Eletrocardiografia/efeitos dos fármacos , Ventrículos do Coração/efeitos dos fármacos , Ventrículos do Coração/patologia , Macrófagos/fisiologia , Masculino , Microscopia , Isquemia Miocárdica/patologia , Necrose , Neutrófilos/fisiologia , Nicorandil/farmacologia , Nifedipino/farmacologia , Músculos Papilares/ultraestrutura , Coelhos , Distribuição Aleatória , Vasodilatadores/farmacologiaRESUMO
OBJECTIVES: To understand papillary muscle malformations, such as in parachute mitral valves or parachute-like asymmetric mitral valves, we studied the development of papillary muscles. METHODS: Normal human hearts at between 5 and 19 weeks of development were studied with immunohistochemistry, three-dimensional reconstructions, and gross inspection. Scanning electron microscopy was used to study human and rat hearts. RESULTS: In embryonic hearts a prominent horseshoe-shaped myocardial ridge runs from the anterior wall through the apex to the posterior wall of the left ventricle. In the atrioventricular region this ridge is continuous with atrial myocardium and covered with cushion tissue. The anterior and posterior parts of the trabecular ridge enlarge and loosen their connections with the atrial myocardium. Their lateral sides gradually delaminate from the left ventricular wall, and the continuity between the two parts is incorporated in the apical trabecular network. In this way the anterior and posterior parts of the ridge transform into the anterolateral and the posteromedial papillary muscles, respectively. Simultaneously, the cushions remodel into valve leaflets and chordae. Only the chordal part of the cushions remains attached to the developing papillary muscles. CONCLUSIONS: Disturbed delamination of the anterior or posterior part of the trabecular ridge from the ventricular wall, combined with underdevelopment of chordae, seems to be the cause of asymmetric mitral valves. Parachute valves, however, develop when the connection between the posterior and anterior part of the ridge condenses to form one single papillary muscle. Thus parachute valves and parachute-like asymmetric mitral valves originate in different ways.
Assuntos
Coração Fetal/embriologia , Valva Mitral/anormalidades , Valva Mitral/embriologia , Músculos Papilares/embriologia , Adulto , Animais , Cordas Tendinosas/anormalidades , Cordas Tendinosas/embriologia , Cordas Tendinosas/ultraestrutura , Feminino , Coração Fetal/anormalidades , Coração Fetal/ultraestrutura , Cardiopatias Congênitas/patologia , Humanos , Processamento de Imagem Assistida por Computador , Imuno-Histoquímica , Microscopia Eletrônica de Varredura , Valva Mitral/ultraestrutura , Músculos Papilares/anormalidades , Músculos Papilares/ultraestrutura , Gravidez , Ratos , Ratos WistarRESUMO
We developed an optical system for the measurement of the Ca2+ content of sarcoplasmic reticulum (SR) in saponin-treated ventricular muscles of ferrets. After the SR was loaded with Ca2+ by activating the Ca2+ pump of SR, caffeine (50 mM) was applied to release the accumulated Ca2+ from the SR into the bathing solution containing the fluorescent Ca2+ indicator, Fluo-3. As Fluo-3, at high concentrations (approximately 200 microM), predominantly binds most of the Ca2+ released from the SR, the Fluo-3 fluorescence change upon Ca2+ binding gave an estimate of the amount of accumulated Ca2+ in SR before caffeine application. The maximal Ca2+ content of SR, thus estimated, was about 370 mumol/l cytoplasm. The amount of Ca2+ loaded in SR showed bell-shaped dependence on the free Ca2+ concentration ([Ca2+]) of the loading solution, reflecting Ca(2+)-induced Ca2+ release at high [Ca2+] (> or = 1 microM). Mg2+ and H+ decreased the rate of Ca2+ uptake by SR. The present system provides a relatively direct means of measurement of the Ca2+ content of SR, and allows examination of the effects of various interventions on SR Ca2+ uptake, bypassing the large influence of intracellular Ca2+ buffer sites.
Assuntos
Cálcio/análise , Miocárdio/química , Retículo Sarcoplasmático/química , Compostos de Anilina , Animais , Cafeína/farmacologia , Cálcio/metabolismo , ATPases Transportadoras de Cálcio/fisiologia , Furões , Fluorescência , Concentração de Íons de Hidrogênio , Magnésio/farmacologia , Miocárdio/metabolismo , Miocárdio/ultraestrutura , Músculos Papilares/química , Músculos Papilares/metabolismo , Músculos Papilares/ultraestrutura , Retículo Sarcoplasmático/metabolismo , Retículo Sarcoplasmático/ultraestrutura , XantenosRESUMO
Several investigators have found experimentally that the force-time integral varies non-linearly with energy expenditure over the course of a cardiac contraction. Also, recent research findings have indicated that the crossbridge cycle to ATP hydrolysis ratio in muscle fiber systems may not be coupled with a one-to-one ratio. In order to investigate these findings, Huxley's sliding filament crossbridge muscle model coupled with parallel and series elastic components was simulated to examine the behavior of the crossbridge energy utilization and force-time integral vs time. Crossbridge (CB) energy utilization was determined by considering the ATP hydrolysis for the crossbridge cycling, and this CB energy was compared with the force-length energy in a contraction. This CB energy was calculated in both isometric and isotonic contractions as a function of contraction time and compared to the force-time integral. Simulation results demonstrated that the ratio of the force-time integral to CB energy varies strongly throughout the cardiac cycle for both isometric and isotonic cases, as has been observed experimentally. Simulations also showed that using the force-length energy component of energy vs the CB energy gave a better correlation between the total energetic predictions and the force-time integral, agreeing with recent finding that the crossbridge cycle to ATP hydrolysis ratio may not be coupled one-to-one, especially at lower force levels.
Assuntos
Metabolismo Energético/fisiologia , Modelos Cardiovasculares , Contração Miocárdica/fisiologia , Miocárdio/metabolismo , Músculos Papilares/metabolismo , Músculos Papilares/fisiologia , Actinas/metabolismo , Trifosfato de Adenosina/metabolismo , Animais , Metabolismo Basal/fisiologia , Cálcio/metabolismo , Simulação por Computador , Cães , Elasticidade , Frequência Cardíaca/fisiologia , Hidrólise , Contração Isométrica/fisiologia , Contração Isotônica/fisiologia , Miofibrilas/metabolismo , Miofibrilas/fisiologia , Miofibrilas/ultraestrutura , Miosinas/metabolismo , Consumo de Oxigênio/fisiologia , Músculos Papilares/ultraestrutura , Sarcômeros/metabolismo , Sarcômeros/fisiologia , Sarcômeros/ultraestruturaRESUMO
UNLABELLED: The contractile behaviour of demembranized atrial and ventricular myocardium of 7 patients transplanted for end-stage heart failure (ESHF) was analyzed. Atrial muscle specimens of patients undergoing coronary artery bypass surgery (n = 9) and pig papillary muscle were used as reference preparations (n = 9). Extreme care was taken for dissection and mounting the muscle fibres (0.3 x 6 mm) in order to keep the passive series compliance small. Calcium sensitivity, cross-bridge cycling rate (estimated by the force-clamping technique and calculation of the shortening velocity at zero load [Vmax]) and isometric force development were measured. Analysis on light- and electronmicroscopic level was carried out. RESULTS: 1) Calcium sensitivity was not altered in ESHF patients; 2) the velocity of the force generating process (cross-bridge cycling rate) was normal in ventricular and reduced in atrial ESHF myocardium, 3) maximum isometric force development was reduced in ventricular, but not in atrial myocardium of ESHF patients, and 4) Vmax was significantly reduced in ventricular and atrial ESHF myocardium (p < 0.0001). Perimysial and endomysial fibrosis was present in ventricular, not in atrial myocardium of ESHF patients. CONCLUSION: A normal cross-bridge cycling rate in left-ventricular ESHF myocardium combined with a decreased capability of muscle shortening indicates the presence of a resistance against shortening localized either on the cross-bridge level or/and due to intra- and pericellular fibrosis. Left-ventricular contractile dysfunction in patients with end-stage heart failure may be related to a normal contractile apparatus contracting within an abnormal intracellular or interstitial environment.
Assuntos
Cardiomiopatia Dilatada/fisiopatologia , Coração/fisiopatologia , Contração Miocárdica/fisiologia , Animais , Cálcio/fisiologia , Estudos de Casos e Controles , Doença das Coronárias/fisiopatologia , Feminino , Humanos , Técnicas In Vitro , Contração Isométrica/fisiologia , Contração Isotônica/fisiologia , Masculino , Microscopia Eletrônica , Pessoa de Meia-Idade , Miocárdio/ultraestrutura , Músculos Papilares/fisiologia , Músculos Papilares/fisiopatologia , Músculos Papilares/ultraestrutura , SuínosRESUMO
To clarify the full picture of the connectin (titin) filament network in situ, we selectively removed actin and myosin filaments from cardiac muscle fibers by gelsolin and potassium acetate treatment, respectively, and observed the residual elastic filament network by deep-etch replica electron microscopy. In the A bands, elastic filaments of uniform diameter (6-7 nm) projecting from the M line ran parallel, and extended into the I bands. At the junction line in the I bands, which may correspond to the N2 line in skeletal muscle, individual elastic filaments branched into two or more thinner strands, which repeatedly joined and branched to reach the Z line. Considering that cardiac muscle lacks nebulin, it is very likely that these elastic filaments were composed predominantly of connectin molecules; indeed, anti-connectin monoclonal antibody specifically stained these elastic filaments. Further, striations of approximately 4 nm, characteristic of isolated connectin molecules, were also observed in the elastic filaments. Taking recent analyses of the structure of isolated connectin molecules into consideration, we concluded that individual connectin molecules stretched between the M and Z lines and that each elastic filament consisted of laterally-associated connectin molecules. Close comparison of these images with the replica images of intact and S1-decorated sarcomeres led us to conclude that, in intact sarcomeres, the elastic filaments were laterally associated with myosin and actin filaments in the A and I bands, respectively. Interestingly, it was shown that the elastic property of connectin filaments was not restricted by their lateral association with actin filaments in intact sarcomeres. Finally, we have proposed a new structural model of the cardiac muscle sarcomere that includes connectin filaments.
Assuntos
Citoesqueleto de Actina/ultraestrutura , Actinas/fisiologia , Miosinas/fisiologia , Músculos Papilares/ultraestrutura , Sarcômeros/ultraestrutura , Actinas/isolamento & purificação , Animais , Anticorpos Monoclonais , Elasticidade , Eletroforese em Gel de Poliacrilamida , Técnica de Congelamento e Réplica , Immunoblotting , Microscopia Eletrônica , Microscopia Imunoeletrônica , Modelos Estruturais , Miosinas/isolamento & purificação , CoelhosRESUMO
The authors carried out ultrastructural studies of the myocardial sections from inbred Wistar rats in the course of acute experimental poisoning with ethylene glycol. It was shown that slight mitochondrial swelling with clearing of the matrix, myofibrillar edema with decreased electron density of the sarcoplasma and widening of channels of the smooth intraplasmatic reticulum were visible as early as at 12 hours after intoxication with no changes in light microscopy. The changes were located mainly in the subendocardial layer of the ventricles and papillary muscles. At later stages of the experimental ultrastructural changes markedly progressed. Mitochondrial swelling enhanced with destruction of mitochondrial crests, myelin-like figures formed, myofibrillar necrosis and contraction bands developed and segmental or complete dissection of the intercalated disk edges appeared. The chages were scattered all over the myocardium predominating in the subendocardial layer and papillary muscles.
Assuntos
Modelos Animais de Doenças , Etilenoglicóis/intoxicação , Mitocôndrias Cardíacas/efeitos dos fármacos , Miocárdio/ultraestrutura , Miofibrilas/efeitos dos fármacos , Músculos Papilares/efeitos dos fármacos , Doença Aguda , Animais , Feminino , Masculino , Microscopia Eletrônica , Mitocôndrias Cardíacas/ultraestrutura , Dilatação Mitocondrial/efeitos dos fármacos , Miofibrilas/ultraestrutura , Músculos Papilares/ultraestrutura , Ratos , Ratos Wistar , Fatores de TempoRESUMO
The heat generated by right ventricular papillary muscles of rabbits was measured after adenosine triphosphate (ATP) splitting by the contractile proteins was chemically inhibited. This tension-independent heat (TIH) (1 mJ/g wet weight) was used to calculate the total calcium (Ca) cycled in a muscle twitch by assuming that 87% of TIH was due to Ca2+ transport by the sarcoplasmic reticulum with a coupling ratio of 2 Ca2+/ATP split; the enthalpy of creatine phosphate hydrolysis buffering ATP was taken as -34 KJ/mol. The estimated Ca turnover per muscle twitch at 21 degrees C, 0.2 Hz pacing rate, and 2.5 mM Ca in the Krebs solution was approximately equal to 50 nmol/g wet weight. There was a tight positive correlation between TIH and mechanical activation during steady-state measurements but no correlation during the sharp increase in mechanical activation (treppe) when stimulation was resumed after a rest period. It is suggested that while total Ca cycling remains unchanged during the initial period of tension treppe, the free Ca2+ transient and mechanical activation increase sharply due to resaturation of high affinity Ca2+ buffers, other than troponin C, depleted of Ca2+ during the rest period.
Assuntos
Cálcio/farmacocinética , Contração Miocárdica/fisiologia , Músculos Papilares/fisiologia , Citoesqueleto de Actina/enzimologia , Citoesqueleto de Actina/metabolismo , Trifosfato de Adenosina/farmacocinética , Animais , ATPases Transportadoras de Cálcio/farmacocinética , Estimulação Elétrica , Temperatura Alta , Músculos Papilares/metabolismo , Músculos Papilares/ultraestrutura , Coelhos , Retículo Sarcoplasmático/enzimologia , Retículo Sarcoplasmático/metabolismoRESUMO
The mechanism of twitch prolongation of hypoxic myocardium after reoxygenation was studied before and after interventions that affect cellular cyclic nucleotide levels, subcellular calcium handling, or oxygen-derived free radical production/survival. Right ventricular ferret papillary muscles were subjected to two 20-minute periods of hypoxia, each followed by 1 hour of reoxygenation. The first sequence of hypoxia/reoxygenation was done without intervention. Before the second sequence, the pharmacological agent under study was added to the superfusate or the superfusate calcium concentration was increased from 2.5 to 8 mM. Time from peak to 80% decline in twitch tension was measured in the presence and absence of each intervention immediately before each period of hypoxia and after reoxygenation at maximal twitch prolongation. Interventions that affect Ca2+ flux across the sarcolemma (verapamil and 8 mM [Ca2+]o) or agents that affect oxygen free radical production/survival (dimethyl sulfoxide and allopurinol) did not affect twitch prolongation. Pharmacological agents that increase cyclic AMP levels (forskolin and milrinone) or those that inhibit mitochondrial activity (oligomycin B and ruthenium red) attenuated twitch prolongation. Pharmacological agents that decrease cyclic AMP levels (carbachol) or inhibit function of the sarcoplasmic reticulum (ryanodine) augmented twitch prolongation. The effect of mitochondrial inhibitors on intracellular calcium handling during hypoxia and reoxygenation was examined using muscles loaded with the bioluminescent calcium indicator aequorin. Mitochondrial inhibitors abbreviated the calcium transient and maximal twitch prolongation after hypoxia. We conclude that alterations in sarcoplasmic reticulum and mitochondria calcium handling contribute to the prolonged relaxation seen upon reoxygenation of hypoxic myocardium.
Assuntos
Cálcio/metabolismo , Cardiomiopatias/metabolismo , Hipóxia/metabolismo , Mitocôndrias Cardíacas/metabolismo , Consumo de Oxigênio , Retículo Sarcoplasmático/metabolismo , Animais , Cálcio/fisiologia , AMP Cíclico/metabolismo , Furões , Radicais Livres , Masculino , Mitocôndrias Cardíacas/efeitos dos fármacos , Mitocôndrias Cardíacas/fisiologia , Contração Miocárdica , Oxigênio/metabolismo , Músculos Papilares/metabolismo , Músculos Papilares/ultraestrutura , Fatores de TempoRESUMO
Myocardial ischemic injury results in altered membrane integrity, energy depletion, and electrolyte shifts leading to accumulation of intracellular Ca. However, analysis of the direct effects of Ca accumulation is complicated by other concomitant cellular changes produced by ischemia. The purpose of this study was to examine the effects of Ca loading in rat papillary muscles produced by Na+-K+ pump inhibition in oxygenated K+-free buffer. Changes in contractile characteristics, high energy phosphate, and elemental concentrations of subcellular compartments were measured. Electron probe X-ray microanalysis was used to assess elemental concentrations in cryosections. After 3 h of Na+-K+ pump inhibition, resting tension (RT) increased to 164% and developed tension (DT) fell to 16.8% of control values. One hour after return to complete buffer, RT and DT partially recovered but remained significantly different from the 180 to 240-min values for the control muscles. Electron probe X-ray microanalysis showed increases in cytoplasmic and mitochondrial Na and Ca and a decrease in K during Na+-K+ pump inhibition. Mitochondrial Ca was greater than 100-fold greater than Ca in control mitochondria. Morphologically, the majority of cells showed ultrastructural damage. The mean ATP level was 20% of control. After 1 h of recovery, the cells appeared more heterogeneous, and the mean mitochondrial Ca decreased, whereas mean cytoplasmic Ca increased. Further statistical analysis showed a bimodal distribution for Na, Ca, K, Mg, and Cl, which coincided with the morphologically mixed population of cells. This suggests that replacement of extracellular K+ was associated with restored electrolyte gradients in some cells and the persistent or further alteration of electrolytes in others. These results suggest that variable Ca accumulation and associated ATP depletion without the compounding effects of ischemia lead to cell injury similar to reperfusion injury reported in ischemic myocardium.
Assuntos
Contração Miocárdica , Músculos Papilares/fisiologia , Canais de Potássio/fisiologia , Canais de Sódio/fisiologia , Trifosfato de Adenosina/metabolismo , Animais , Eletrólitos/metabolismo , Microanálise por Sonda Eletrônica , Feminino , Microscopia Eletrônica de Varredura , Músculos Papilares/citologia , Músculos Papilares/ultraestrutura , Ratos , Ratos EndogâmicosRESUMO
Biopsy material of the hypertrophied human papillary muscle has been processed according to various electron microscopical techniques in order to study the mitochondrial ultrastructure and the association between mitochondria and sarcoplasmic reticulum (SR). En bloc staining with a Cu-Pb citrate solution resulted in specifically contrasted mitochondrial and sarcotubular membranes, characterized by numerous, discrete, electron-dense particles. The differences in staining patterns between the perinuclear mitochondria and their subsarcolemmal and interfibrillar counterparts suggest differences in chemical properties and/or metabolic activities. The selectively contrasted mitochondrial particles may represent a conglomerate of extrinsic and intrinsic respiratory enzymes and other membrane-associated proteins, while the majority of the electron-dense particles of the sarcotubular membrane may represent positively stained Ca2+-pumps. Ultrastructural findings in the present study strongly indicate that the slender mitochondrial projections represent an initial stage in a process leading to the formation of large and pleomorphic mitochondria. Intimate contact between adjacent mitochondria as well as between mitochondria and SR are documented. In the contact regions some of the specifically contrasted particles of the adjacent membranes had fused with each other. It is suggested that these particles represent membrane-bound transport proteins providing a system for inter-organelle exchange of metabolites and/or ions.
Assuntos
Cardiomegalia/patologia , Mitocôndrias Cardíacas/ultraestrutura , Músculos Papilares/ultraestrutura , Retículo Sarcoplasmático/ultraestrutura , Adulto , Humanos , Microscopia Eletrônica , Coloração e RotulagemRESUMO
Morphometric data on left ventricular papillary muscle structures have been determined in tumor-induced malnutrition and related to the maximum activities of key enzymes for energy production in the whole myocardium. Adult, nongrowing mice with a syngeneic sarcoma were used to represent a condition of cancer associated host tissue wasting. Hearts from mice 11 days after tumor implantation showed atrophy and a significantly reduced amount of myofibrillar, soluble, and collagen proteins than hearts from control animals. The cross-sectional area of myocardial cells was 33% smaller in tumor-bearing mice (p less than 0.025), but the total number of capillaries and the residual interstitial volume were similar in the two groups. The total number of subcellular structures per cell, such as mitochondria, myofibrils, and myosin filaments per myofiber, were significantly lower in the tumor-bearing animals (p less than 0.025). Conversely, the proportion of myofibrils was higher (p less than 0.05) in tumor-bearing animals while the proportion of mitochondria was lower. Maximum activities (Vmax) of selected regulatory key enzymes for energy production (glycogenolytic, glycolytic, and mitochondrial) were not significantly altered in hearts from tumor-bearing mice. The results support the conclusion that myocardial functional capacity is better preserved than overall structural components would imply in tumor-host associated malnutrition, which is probably secondary to deprived food intake. Teleologically, this may be a means by which functional deterioration of the heart is minimized during the induction of malnutrition.
Assuntos
Metabolismo Energético , Miocárdio/ultraestrutura , Distúrbios Nutricionais/etiologia , Sarcoma Experimental/complicações , Animais , Caquexia/etiologia , Caquexia/metabolismo , Caquexia/patologia , Feminino , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Microscopia Eletrônica , Mitocôndrias Cardíacas/enzimologia , Mitocôndrias Cardíacas/metabolismo , Mitocôndrias Cardíacas/ultraestrutura , Miocárdio/enzimologia , Distúrbios Nutricionais/metabolismo , Distúrbios Nutricionais/patologia , Músculos Papilares/enzimologia , Músculos Papilares/ultraestrutura , Sarcoma Experimental/metabolismoRESUMO
Anatomically and biochemically distinct populations of cardiac mitochondria have been isolated from a number of animal species. The physiologic differences between subsarcolemmal (SS) and interfibrillar (IF) mitochondria, coupled with their different location within the cytomatrix, have led to speculation about possible specificities of function within the myocardial cell. To date, these two mitochondrial subpopulations have not been demonstrated in human cardiac tissue. Subsarcolemmal and interfibrillar cardiac mitochondria were isolated from papillary muscle removed from five patients undergoing mitral valve replacement surgery. Mitochondrial respiratory activity was determined polarographically. IF mitochondria had significantly higher state 3 (ADP-dependent) rates of respiration then SS mitochondria (116.7 +/- 7.1 versus 86.5 +/- 8.3 ng atoms or oxygen per minute per milligram mitochondrial protein; P less than 0.05 [mean +/- SE]). These data agree with similar studies performed in other animal species and support the concept of distinct subpopulations of mitochondria within the human myocardial cell.