American Journal of Physiology最新文献

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Calcium transients in single fibers of low-frequency stimulated fast-twitch muscle of rat. 低频刺激大鼠快缩肌单纤维钙瞬变。
American Journal of Physiology Pub Date : 1999-12-01 DOI: 10.1152/ajpcell.1999.277.6.C1122
S Carroll, P Nicotera, D Pette
{"title":"Calcium transients in single fibers of low-frequency stimulated fast-twitch muscle of rat.","authors":"S Carroll,&nbsp;P Nicotera,&nbsp;D Pette","doi":"10.1152/ajpcell.1999.277.6.C1122","DOIUrl":"https://doi.org/10.1152/ajpcell.1999.277.6.C1122","url":null,"abstract":"<p><p>Ca(2+) transients were investigated in single fibers isolated from rat extensor digitorum longus muscles exposed to chronic low-frequency stimulation for different time periods up to 10 days. Approximately 2.5-fold increases in resting Ca(2+) concentration ([Ca(2+)]) were observed 2 h after stimulation onset and persisted throughout the stimulation period. The elevated [Ca(2+)] levels were in the range characteristic of slow-twitch fibers from soleus muscle. In addition, we noticed a transitory elevation of the integral [Ca(2+)] per pulse with a maximum ( approximately 5-fold) after 1 day. Steep decreases in rate constant of [Ca(2+)] decay could be explained by an immediate impairment of Ca(2+) uptake and, with longer stimulation periods, by an additional loss of cytosolic Ca(2+) binding capacity resulting from a decay in parvalbumin content. A partial recovery of the rate constant of [Ca(2+)] decay in 10-day stimulated muscle could be explained by an increasing mitochondrial contribution to Ca(2+) sequestration.</p>","PeriodicalId":7590,"journal":{"name":"American Journal of Physiology","volume":"277 6","pages":"C1122-9"},"PeriodicalIF":0.0,"publicationDate":"1999-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1152/ajpcell.1999.277.6.C1122","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21458680","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 64
Effect of high-altitude acclimation on NEFA turnover and lipid utilization during exercise in rats. 高原驯化对运动大鼠NEFA代谢和脂质利用的影响。
American Journal of Physiology Pub Date : 1999-12-01 DOI: 10.1152/ajpendo.1999.277.6.E1095
G B McClelland, P W Hochachka, J M Weber
{"title":"Effect of high-altitude acclimation on NEFA turnover and lipid utilization during exercise in rats.","authors":"G B McClelland,&nbsp;P W Hochachka,&nbsp;J M Weber","doi":"10.1152/ajpendo.1999.277.6.E1095","DOIUrl":"https://doi.org/10.1152/ajpendo.1999.277.6.E1095","url":null,"abstract":"<p><p>Relative exercise intensity (or %maximum O(2) consumption, VO(2 max)) controls fuel selection at sea level (SL) and after high-altitude acclimation (HA) in rats. In this context we used indirect calorimetry, [1-(14)C]palmitate infusions, and muscle triacylglycerol (TAG) measurements to determine 1) total lipid oxidation, 2) the relationship between circulatory nonesterified fatty acid (NEFA) flux and concentration, and 3) muscle TAG depletion after exercise in HA-acclimated rats. Aerobic capacity is decreased in trained rats after 10 wk of acclimation. Both SL and HA showed the same relative use of lipids at 60% [62 +/- 5% (HA) and 61 +/- 3% (SL) of O(2) consumption (VO(2))] and 80% [46 +/- 6% (HA) and 47 +/- 5% (SL) of VO(2)] of their respective VO(2 max). At 60% VO(2 max), plasma [NEFA] were higher in HA, but rate of appearance was essentially the same in both groups (at 30 min, 38 +/- 9 vs. 49 +/- 6 micromol. kg(-1). min(-1) in HA and SL, respectively). At this intensity SL showed no significant decrease in muscle TAG, but in HA it decreased by 64% in soleus and by 90% in red gastrocnemius. We conclude that 1) the relative contributions of total lipid are the same in SL and HA, contrary to differences in [NEFA], because the relationship between flux rate and [NEFA] is modified after acclimation, and 2) muscle TAG may play a more important role at HA.</p>","PeriodicalId":7590,"journal":{"name":"American Journal of Physiology","volume":"277 6","pages":"E1095-102"},"PeriodicalIF":0.0,"publicationDate":"1999-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1152/ajpendo.1999.277.6.E1095","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21457771","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 33
Novel method to estimate ventricular contractility using intraventricular pulse wave velocity. 利用室内脉搏波速度估计心室收缩力的新方法。
American Journal of Physiology Pub Date : 1999-12-01 DOI: 10.1152/ajpheart.1999.277.6.H2409
T Shishido, M Sugimachi, O Kawaguchi, H Miyano, T Kawada, W Matsuura, Y Ikeda, K Sunagawa
{"title":"Novel method to estimate ventricular contractility using intraventricular pulse wave velocity.","authors":"T Shishido,&nbsp;M Sugimachi,&nbsp;O Kawaguchi,&nbsp;H Miyano,&nbsp;T Kawada,&nbsp;W Matsuura,&nbsp;Y Ikeda,&nbsp;K Sunagawa","doi":"10.1152/ajpheart.1999.277.6.H2409","DOIUrl":"https://doi.org/10.1152/ajpheart.1999.277.6.H2409","url":null,"abstract":"<p><p>We developed a novel technique for estimating ventricular contractility using intraventricular pulse wave velocity (PWV). In eight isolated, cross-circulated canine hearts, we used a fast servo pump to inject a volume pulse into the base of the left ventricular chamber at late diastole and at late systole. We measured the transit time of the volume pulse wave as it traversed the distance from base to apex and calculated the intraventricular PWV. The intraventricular PWV increased from diastole (2.3 +/- 0.4 m/s) to systole (11.7 +/- 2.4 m/s, P < 0.0001 vs. diastole). The square of the intraventricular PWV at late systole correlated linearly with the left ventricular end-systolic elastance (r = 0.939, P < 0.0001) and with the end-systolic Young's modulus (r = 0.901, P < 0.0001). Moreover, the intraventricular PWV was insensitive to preload. We conclude that the intraventricular PWV at late systole reflects left ventricular end-systolic elastance reasonably well. The fact that estimation of PWV does not require volume measurement or load manipulation makes this technique an attractive means of assessing ventricular contractility.</p>","PeriodicalId":7590,"journal":{"name":"American Journal of Physiology","volume":"277 6","pages":"H2409-15"},"PeriodicalIF":0.0,"publicationDate":"1999-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1152/ajpheart.1999.277.6.H2409","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21457777","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 9
S-T segment voltage during sequential coronary occlusions is an unreliable marker of preconditioning. 序贯冠状动脉闭塞时S-T段电压是一个不可靠的预适应指标。
American Journal of Physiology Pub Date : 1999-12-01 DOI: 10.1152/ajpheart.1999.277.6.H2435
M Birincioglu, X M Yang, S D Critz, M V Cohen, J M Downey
{"title":"S-T segment voltage during sequential coronary occlusions is an unreliable marker of preconditioning.","authors":"M Birincioglu,&nbsp;X M Yang,&nbsp;S D Critz,&nbsp;M V Cohen,&nbsp;J M Downey","doi":"10.1152/ajpheart.1999.277.6.H2435","DOIUrl":"https://doi.org/10.1152/ajpheart.1999.277.6.H2435","url":null,"abstract":"<p><p>During coronary angioplasty, a stair-step decrease in peak S-T segment elevation from the first to the second coronary occlusion has been assumed to indicate a preconditioning (PC) effect. This association was evaluated with myocardial electrograms in rabbits, which revealed that two sequential 5-min coronary occlusions resulted in a marked decrease in the area under the S-T segment voltage-time curve (P < 0.05) with no change during a third occlusion. Pretreatment with either 5-hydroxydecanoate, a mitochondrial ATP-sensitive potassium (K(ATP)) channel blocker, or anisomycin, an activator of stress-activated protein kinases, had no effect on the stair-step decline in the S-T segment voltage between the first two occlusions. HMR-1883, a potent closer of sarcolemmal K(ATP) channels, abolished changes in S-T segment elevation after brief coronary occlusions but had no effect on the infarct-sparing property of the two preconditioning 5-min occlusions. Interestingly, HMR-1883 blocked myocardial protection from diazoxide, raising doubt that the latter opens only mitochondrial channels. Therefore, myocardial protection and S-T segment changes during ischemia are dissociated. These data suggest that it is the mitochondrial K(ATP) channel that protects the myocardium, and it is the sarcolemmal channel that is responsible for changes in S-T elevation. Therefore, it cannot always be inferred that changes in S-T segment elevation reflect the state of myocardial protection.</p>","PeriodicalId":7590,"journal":{"name":"American Journal of Physiology","volume":"277 6","pages":"H2435-41"},"PeriodicalIF":0.0,"publicationDate":"1999-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1152/ajpheart.1999.277.6.H2435","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21457781","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 47
Prostaglandins buffer ANG II-mediated increases in cytosolic calcium in preglomerular VSMC. 前列腺素缓冲angii介导的肾小球前VSMC中胞质钙的增加。
American Journal of Physiology Pub Date : 1999-12-01 DOI: 10.1152/ajprenal.1999.277.6.F850
K E Purdy, W J Arendshorst
{"title":"Prostaglandins buffer ANG II-mediated increases in cytosolic calcium in preglomerular VSMC.","authors":"K E Purdy,&nbsp;W J Arendshorst","doi":"10.1152/ajprenal.1999.277.6.F850","DOIUrl":"https://doi.org/10.1152/ajprenal.1999.277.6.F850","url":null,"abstract":"<p><p>In order to exert an appropriate biological effect, the action of the vasoconstrictive hormone angiotensin II (ANG II) is modulated by vasoactive factors such as prostaglandins PGE2 and PGI2. The present study investigates whether prostaglandins alter ANG II-mediated increases in cytosolic calcium concentration ([Ca2+]i) in vascular smooth muscle cells (VSMC) isolated from rat renal preglomerular arterioles. [Ca2+]i was assessed using the calcium-sensitive dye fura 2 and a microscope-based photometer system. ANG II (10(-7) M) caused a biphasic, time-dependent [Ca2+]i response: an initial peak increase from 52 +/- 7 to 264 +/- 25 nM, followed by a sustained plateau of 95 +/- 9 nM in cultured VSMC. Coadministration of PGE2 or PGI2 or synthetic mimetics caused dose-dependent decreases in the peak [Ca2+]i response to ANG II, with attenuation of 40-50%. This degree of inhibition was even more pronounced in individual freshly isolated preglomerular VSMC. Increasing cAMP levels in cultured VSMC, by using either a cell-permeable analog or inhibiting phosphodiesterase activity, mirrored the antagonistic effects of prostaglandins on ANG II-stimulated increases in [Ca2+]i. Radioimmunoassays demonstrate that ANG II (10(-7) M) stimulates production of PGI2 and PGE2; the stable prostacyclin metabolite 6-keto-PGF(1alpha) was released in 10-fold greater concentrations than PGE(2.) Indomethacin blockade of prostaglandin production potentiated both the peak (264 to 337 +/- 26 nM) and sustained [Ca2+]i responses (95 to 181 +/- 22 nM) to ANG II. When prostaglandin analogs were added during indomethacin treatment, the ANG II response was restored to the typical pattern. In conclusion, we demonstrate that modulation of intracellular calcium levels is one mechanism by which prostaglandins can buffer ANG II-mediated constriction in renal preglomerular VSMC. PGI2 is more potent than PGE2 in this regard.</p>","PeriodicalId":7590,"journal":{"name":"American Journal of Physiology","volume":"277 6","pages":"F850-8"},"PeriodicalIF":0.0,"publicationDate":"1999-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1152/ajprenal.1999.277.6.F850","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21457790","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 34
Intramyocardial vascular volume distribution studied by synchrotron radiation-excited X-ray fluorescence. 同步辐射激发x射线荧光研究心内血管容积分布。
American Journal of Physiology Pub Date : 1999-12-01 DOI: 10.1152/ajpheart.1999.277.6.H2353
Y Nakajima, N Akizuki, Y Kimura, H Kohguchi, A Tanaka, M Chujo, N Hattan, Y Shinozaki, A Iida, S Handa, H Nakazawa, H Mori
{"title":"Intramyocardial vascular volume distribution studied by synchrotron radiation-excited X-ray fluorescence.","authors":"Y Nakajima,&nbsp;N Akizuki,&nbsp;Y Kimura,&nbsp;H Kohguchi,&nbsp;A Tanaka,&nbsp;M Chujo,&nbsp;N Hattan,&nbsp;Y Shinozaki,&nbsp;A Iida,&nbsp;S Handa,&nbsp;H Nakazawa,&nbsp;H Mori","doi":"10.1152/ajpheart.1999.277.6.H2353","DOIUrl":"https://doi.org/10.1152/ajpheart.1999.277.6.H2353","url":null,"abstract":"<p><p>We evaluated the vascular volume distribution with fine resolution (0.1-1.3 mg myocardial tissue) in the sagittal plane of the left ventricle by using the microsphere filling method in 21 dogs. The coronary arterial volume density in the sagittal plane did not exhibit normal distribution and was characterized by variability among the outer-to-inner layers and within the layers (+2SD/-2SD > 80 times), and the median values in the layers ranged from 4.7 to 22. 9 nl/mg myocardial tissue. The fractal analysis of vascular volume revealed a self-similar nature with a fractal dimension (D value) similar to that of flow distribution (1.20 +/- 0.05 and 1.24 +/- 0. 09 for vascular volume and flow distribution, respectively) and had a more marked variability than the flow. The correlation of the regional vascular volume between adjacent regions decreased as the distance increased. However, the correlation coefficients in the endocardial-to-epicardial direction were significantly higher than those in the anterior-to-posterior direction (P < 0.05 by paired t-test). In conclusion, we determined intramyocardial vascular volume density in the sagittal plane, and the distribution revealed considerable variability, self-similarity, and asymmetry in the correlation among the adjacent regions. These observations could be related to the characteristics of the intramural coronary vascular network.</p>","PeriodicalId":7590,"journal":{"name":"American Journal of Physiology","volume":"277 6","pages":"H2353-62"},"PeriodicalIF":0.0,"publicationDate":"1999-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1152/ajpheart.1999.277.6.H2353","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21457874","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Mechanisms by which insulin, associated or not with glucose, may inhibit hepatic glucose production in the rat. 胰岛素(与葡萄糖相关或不相关)抑制大鼠肝脏葡萄糖生成的机制。
American Journal of Physiology Pub Date : 1999-12-01 DOI: 10.1152/ajpendo.1999.277.6.E984
L Guignot, G Mithieux
{"title":"Mechanisms by which insulin, associated or not with glucose, may inhibit hepatic glucose production in the rat.","authors":"L Guignot,&nbsp;G Mithieux","doi":"10.1152/ajpendo.1999.277.6.E984","DOIUrl":"https://doi.org/10.1152/ajpendo.1999.277.6.E984","url":null,"abstract":"<p><p>We investigated the intrahepatic mechanisms by which insulin, associated or not with hyperglycemia, may inhibit hepatic glucose production (HGP) in the rat. After a hyperinsulinemic euglycemic clamp in postabsorptive (PA) anesthetized rats, the 70% inhibition of HGP could be explained by a dramatic decrease in the glucose 6-phosphate (G-6-P) concentration, whereas the glucose-6-phosphatase (G-6-Pase) and glucokinase (GK) activities were unchanged. Under hyperinsulinemic hyperglycemic condition, the GK flux was increased. The G-6-P concentration was not or only weakly decreased. The inhibition of HGP involved a significant 25% inhibition of the G-6-Pase activity. Under similar conditions in fasted rats, the GK flux was very low. The suppression of G-6-Pase and HGP did not occur, despite plasma insulin and glucose concentrations similar to those in PA rats. Therefore, 1) insulin suppresses HGP in euglycemia by solely decreasing the G-6-P concentration; 2) when combining both hyperinsulinemia and hyperglycemia, the suppression of HGP involves the inhibition of the G-6-Pase activity; and 3) a sustained glucose-phosphorylation flux might be a crucial determinant in the inhibition of G-6-Pase and of HGP.</p>","PeriodicalId":7590,"journal":{"name":"American Journal of Physiology","volume":"277 6","pages":"E984-9"},"PeriodicalIF":0.0,"publicationDate":"1999-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1152/ajpendo.1999.277.6.E984","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21458509","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 57
Restricted fetal growth and the response to dietary cholesterol in the guinea pig. 豚鼠胎儿生长受限及对膳食胆固醇的反应。
American Journal of Physiology Pub Date : 1999-12-01 DOI: 10.1152/ajpregu.1999.277.6.R1675
K L Kind, P M Clifton, A I Katsman, M Tsiounis, J S Robinson, J A Owens
{"title":"Restricted fetal growth and the response to dietary cholesterol in the guinea pig.","authors":"K L Kind,&nbsp;P M Clifton,&nbsp;A I Katsman,&nbsp;M Tsiounis,&nbsp;J S Robinson,&nbsp;J A Owens","doi":"10.1152/ajpregu.1999.277.6.R1675","DOIUrl":"https://doi.org/10.1152/ajpregu.1999.277.6.R1675","url":null,"abstract":"<p><p>Epidemiological studies suggest that retarded growth before birth is associated with increased plasma total and low-density lipoprotein (LDL) cholesterol concentrations in adult life. Thus perturbations of prenatal growth may permanently alter cholesterol metabolism. To determine directly whether restriction of prenatal nutrition and growth alters postnatal cholesterol homeostasis, the plasma cholesterol response to cholesterol feeding (0.25% cholesterol) was examined in adult guinea pig offspring of ad libitum-fed or moderately undernourished mothers. Maternal undernutrition (85% ad libitum intake throughout pregnancy) reduced birth weight (-13%). Plasma total cholesterol was higher prior to and following 6 wk cholesterol feeding in male offspring of undernourished mothers compared with male offspring of ad libitum-fed mothers (P < 0.05). The influence of birth weight on cholesterol metabolism was examined by dividing the offspring into those whose birth weight was above (high) or below (low) the median birth weight. Plasma total cholesterol concentrations prior to cholesterol feeding did not differ with size at birth, but plasma total and LDL cholesterol were 31 and 34% higher, respectively, following cholesterol feeding in low- compared with high-birth weight males (P < 0.02). The response to cholesterol feeding in female offspring was not altered by variable maternal nutrition or size at birth. Covariate analysis showed that the effect of maternal undernutrition on adult cholesterol metabolism could be partly accounted for by alterations in prenatal growth. In conclusion, maternal undernutrition and small size at birth permanently alter postnatal cholesterol homeostasis in the male guinea pig.</p>","PeriodicalId":7590,"journal":{"name":"American Journal of Physiology","volume":"277 6","pages":"R1675-82"},"PeriodicalIF":0.0,"publicationDate":"1999-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1152/ajpregu.1999.277.6.R1675","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21458525","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 100
Effects of modest anemia on systemic and coronary circulation of septic sheep. 中度贫血对脓毒性绵羊全身循环和冠状动脉循环的影响。
American Journal of Physiology Pub Date : 1999-12-01 DOI: 10.1152/ajpheart.1999.277.6.H2195
F Bloos, C M Martin, C G Ellis, W J Sibbald
{"title":"Effects of modest anemia on systemic and coronary circulation of septic sheep.","authors":"F Bloos,&nbsp;C M Martin,&nbsp;C G Ellis,&nbsp;W J Sibbald","doi":"10.1152/ajpheart.1999.277.6.H2195","DOIUrl":"https://doi.org/10.1152/ajpheart.1999.277.6.H2195","url":null,"abstract":"<p><p>Although a lower transfusion trigger is generally recommended, little evidence is available about the physiological mechanisms of mild anemia in diseases with an imbalance between O2 supply and O2 demand such as sepsis. This study was undertaken to describe the systemic and coronary metabolic O2 reserve in an awake sheep model of hyperdynamic sepsis comparing two different hemoglobin levels. Twenty-four hours after sheep were rendered septic by cecal ligation and perforation (CLP), blood transfusion (n = 7, hemoglobin = 120 g/l) and isovolemic hemodilution (n = 8, hemoglobin = 70 g/l), respectively, were performed. Another 24 h later, we measured hemodynamics, organ blood flows, and systemic and myocardial O2 metabolism variables at baseline and through four stages of progressive hypoxia. Maximum coronary blood flow was 766.3 +/- 87.4 ml. min(-1). 100 g(-1) in hemodiluted sheep group versus 422.7 +/- 53.7 ml. min(-1). 100 g(-1) in the transfused sheep (P < 0.01). Myocardial O2 extraction was higher in the transfusion group (P = 0.03) throughout the whole hypoxia trial. In the hemodilution group, coronary blood flow increased more per increase in myocardial O(2) uptake than in transfused sheep (P < 0.01). This was accompanied by a lower left ventricular epicardial-to-endocardial flow ratio in hemodiluted sheep (1.13 +/- 0.07) than in transfused sheep (1.34 +/- 0.02, P < 0.05). We conclude that the lower coronary blood flow and greater myocardial O2 extraction in transfused septic sheep preserves transmyocardial O2 metabolism better in comparison to hemodiluted sheep.</p>","PeriodicalId":7590,"journal":{"name":"American Journal of Physiology","volume":"277 6","pages":"H2195-204"},"PeriodicalIF":0.0,"publicationDate":"1999-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1152/ajpheart.1999.277.6.H2195","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21458555","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Functional role of ionic regulation of Na+/Ca2+ exchange assessed in transgenic mouse hearts. 离子调控在转基因小鼠心脏中Na+/Ca2+交换的功能作用
American Journal of Physiology Pub Date : 1999-12-01 DOI: 10.1152/ajpheart.1999.277.6.H2212
K Maxwell, J Scott, A Omelchenko, A Lukas, L Lu, Y Lu, M Hnatowich, K D Philipson, L V Hryshko
{"title":"Functional role of ionic regulation of Na+/Ca2+ exchange assessed in transgenic mouse hearts.","authors":"K Maxwell,&nbsp;J Scott,&nbsp;A Omelchenko,&nbsp;A Lukas,&nbsp;L Lu,&nbsp;Y Lu,&nbsp;M Hnatowich,&nbsp;K D Philipson,&nbsp;L V Hryshko","doi":"10.1152/ajpheart.1999.277.6.H2212","DOIUrl":"https://doi.org/10.1152/ajpheart.1999.277.6.H2212","url":null,"abstract":"<p><p>Na+/Ca2+ exchange is the primary mechanism mediating Ca2+ efflux from cardiac myocytes during diastole and, thus, can prominently influence contractile force. In addition to transporting Na+ and Ca2+, the exchanger is also regulated by these ions. Although structure-function studies have identified protein regions of the exchanger subserving these regulatory processes, their physiological importance is unknown. In this study, we examined the electrophysiological and mechanical consequences of cardiospecific overexpression of the canine cardiac exchanger NCX1.1 and a deletion mutant of NCX1.1 (Delta680-685), devoid of intracellular Na+ (Na+i)- and Ca2+ (Ca2+i)- dependent regulatory properties, in transgenic mice. Using the giant excised patch-clamp technique, normal ionic regulation was observed in membrane patches from cardiomyocytes isolated from control and transgenic mice overexpressing NCX1.1. In contrast, ionic regulation was nearly abolished in mice overexpressing Delta680-685, indicating that the native regulatory processes could be overwhelmed by expression of the transgene. To address the physiological consequences of ionic regulation of the Na+/Ca2+ exchanger, we examined postrest force development in papillary muscles from NCX1.1 and Delta680-685 transgenic mice. Postrest potentiation was found to be substantially greater in Delta680-685 than in NCX1.1 transgenic mice, supporting the notion that ionic regulation of Na+/Ca2+ exchange plays a significant functional role in cardiac contractile properties.</p>","PeriodicalId":7590,"journal":{"name":"American Journal of Physiology","volume":"277 6","pages":"H2212-21"},"PeriodicalIF":0.0,"publicationDate":"1999-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1152/ajpheart.1999.277.6.H2212","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21458557","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 25
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