Simulated microgravity increases myogenic tone in rat cerebral arteries

Adaptation ofthe cerebral circulation to microgravity was investigated in rat middlecerebral arteries after 20 days of hindlimb unweighting (HU). Myogenicresponses were measured in isolated, pressurized arteries from HU andcontrol animals. Maximal passive lumen diameters, obtained in theabsence of extracellular Ca²⁺ plusEDTA, were not significantly different between groups (249 vs. 258 µm). In physiological salt solution, arteries from both HU andcontrol animals maintained a constant lumen diameter when subjected toincremental increases in transmural pressure (20-80 mmHg).However, the diameter of arteries from HU animals was significantly smaller than that of arteries from control animals at all pressures; this difference could be eliminated by exposure to the nitric oxidesynthase inhibitorN^G-nitro-L-argininemethyl ester. After HU treatment, transient distensibility of theartery wall in response to pressure was also significantly decreased,whereas the frequency and amplitude of vasomotion were increased. Thelatter changes were not affected byN^G-nitro-L-argininemethyl ester. Thus simulated microgravity increases cerebral arterymyogenic tone through both nitric oxide synthase-dependent and-independent mechanisms.

     

Vascular hyporesponsiveness in simulated microgravity: role of nitric oxide-dependent mechanisms.

Simulated microgravity depresses the ability of arteries to constrict to norepinephrine (NE). In the present study the role of nitric oxide-dependent mechanisms on the vascular hyporesponsiveness to NE was investigated in peripheral arteries of the rat after 20 days of hindlimb unweighting (HU). Blood vessels from control rats and rats subjected to HU (HU rats) were cut into 3-mm rings and mounted in tissue baths for the measurement of isometric contraction. Mechanical removal of the endothelium from carotid artery rings, but not from aorta or femoral artery rings, of HU rats restored the contractile response to NE toward control. A 10-fold increase in sensitivity to ACh was observed in phenylephrine-precontracted carotid artery rings from HU rats. In the presence of the nitric oxide synthase (NOS) substrate L-arginine, the inducible NOS inhibitor aminoguanidine (AG) restored the contractile responses to NE to control levels in the femoral, but not carotid, artery rings from HU rats. In vivo blood pressure measurements revealed that the peak blood pressure increase to NE was significantly greater in the control than in the HU rats, but that to AG was less than one-half in control compared with HU rats. These results indicate that the endothelial vasodilator mechanisms may be upregulated in the carotid artery, whereas the inducible NOS expression/activity may be increased in the femoral artery from HU rats. These HU-mediated changes could produce a sustained elevation of vascular nitric oxide levels that, in turn, could contribute to the vascular hyporesponsiveness to NE.     

Mechanism of the exercise hyperkalemia: an alternate hypothesis

Wasserman, Karlman, William W. Stringer, Richard Casaburi,and Yong-Yu Zhang. Mechanism of the exercisehyperkalemia: an alternate hypothesis. J. Appl.Physiol. 83(2): 631-643, 1997.A progressivehyperkalemia is observed as exercise intensity increases. The currentmost popular hypothesis for the hyperkalemia is that theNa⁺-K⁺pump cannot keep pace with the K⁺efflux from muscle during the depolarization-repolarization process ofthe sarcolemmal membrane during muscle contraction. In this report, wepresent data that suggest an alternate hypothesis to those previouslydescribed. Because phosphocreatine (PCr) is a highly dissociated acidand creatine is neutral at cell pH, the concentration of nondiffusibleanions decreases, and an alkaline reaction takes place when PCrhydrolyzes. This creates a state of cation(K⁺) excess andH⁺ depletion in the cell. Toexamine the balance of K⁺ andH⁺ for exercising muscle duringthe early period of exercise when PCr changes most rapidly, catheterswere inserted into the brachial artery and femoral vein (FV) in fivehealthy subjects who performed two 6-min cycle ergometer exercise testsat 40 and 85% of peak oxygen uptake. FV blood was sampled every 5 sduring the first 2 min, then every 30 s for the remaining 4 min ofexercise and the first 3 min of recovery, and then less frequently forthe next 12 min. Arterial sampling was every 30 s during exercise andsimultaneous with FV sampling during recovery. ArterialK⁺ concentration([K⁺]) increase laggedFV [K⁺]increase. The hyperkalemia observed during early exerciseresults from K⁺ release fromskeletal muscle. FV[K⁺] increased by 5 sof the start of exercise and followed the rate ofH⁺ loss from the FV blood for thefirst 30 s of exercise. FV lactate andNa⁺ kinetics differed fromK⁺ kinetics during exercise andrecovery. As predicted from the PCr hydrolysis reaction, the exercisinglimb took up H⁺ and releasedK⁺ at the start of exercise (first30 s) at both exercise intensities, resulting in a FV metabolicalkalosis. K⁺ release wasessentially complete by 3 min, the time at which oxygen uptake (and,presumably, PCr) reached its asymptote. These findings lead us tohypothesize that the early K⁺release by the cell takes place withH⁺ exchange and that the majormechanism for the exercise hyperkalemia is the reduction innondiffusible intracellular anions in the myocyte as PCr hydrolyzes.

     

Differential modulation of caffeine- and IP3-induced calcium release in cultured arterial tissue

To investigatethe Ca²⁺-dependent plasticity ofsarcoplasmic reticulum (SR) function in vascular smooth muscle,transient responses to agents releasing intracellularCa²⁺ by either ryanodine(caffeine) orD-myo-inositol1,4,5-trisphosphate [IP₃;produced in response to norepinephrine (NE),5-hydroxytryptamine (5-HT), arginine vasopressin (AVP)] receptorsin rat tail arterial rings were evaluated after 4 days of organculture. Force transients induced by all agents were increased comparedwith those induced in fresh rings. Stimulation by 10% FCSduring culture further potentiated the force andCa²⁺ responses to caffeine (20 mM)but not to NE (10 µM), 5-HT (10 µM), or AVP (0.1 µM). The effectwas persistent, and SR capacity was not altered after reversibledepletion of stores with cyclopiazonic acid. The effects of serum couldbe mimicked by culture in depolarizing medium (30 mMK⁺) and blocked by the additionof verapamil (1 µM) or EGTA (1 mM) to the medium, loweringintracellular Ca²⁺ concentration([Ca²⁺]_i)during culture. These results show that modulation of SR function canoccur in vitro by a mechanism dependent on long-term levels of basal[Ca²⁺]_iand involving ryanodine- but notIP₃ receptor-mediatedCa²⁺release.     

Different responsiveness of a variety of isolated dog arteries to prostaglandin D3

The addition of prostaglandin (PG) D₂ contracted helical strips of dog cerebral, coronary, renal and femoral arteries; the contraction was greatest in cerebral arteries. The contractile response of cerebral arteries was potentiated by aspirin and attenuated by polyphloretin phosphate. In the arterial strips contracted with PGF_2α, PGD₂ elicited a concetration-related relaxation; the relaxation was greatest in mesenteric arteries. In mesenteric arterial strips contracted with norepinephrine, a lesser degree of relaxation was induced, and in the K⁺-contracted arteries, only a contraction was induced. Treatment with PGD₂ attenuated the contractile responses of cerebral and mesentric arteries to PGF_2α or PGE₂; this inhibitory effect was approximately 10 times greater in mesenteric arteries. However, the response to serotonin (for cerebral arteries) or norepinephrine (for mesenteric) was unaffected. It may be concluded that the heterogeneity of response to PGD₂ of a variety of dog arteries is due to different contributions of vasoconstrictor and vasodilator mechanisms. PGD₂ appears top share the mechanism underlying arterial contraction with PGF_2α and PGE₂, and interferes with the effect of these PG's possibly on receptor sites.     

NAD(P)H oxidase inhibiting with apocynin improved vascular reactivity in tail-suspended hindlimb unweighting rat

Recent studies suggested that reactive oxygen species derived from nicotinamide adenine dinucleotide phosphate (NAD(P)H) oxidase is of functional importance in modulating vascular tone, and we have previously detected excessive superoxide production in tail-suspended hindlimb unweighting (HU) rat cerebral and carotid arteries. HU rat was a widely used model to simulate physiological effects on the vasculature. The present study tended to investigate whether NAD(P)H oxidase inhibition with apocynin influences vasoconstriction, endothelium-dependent relaxation, and nitrite/nitrate (NOx) content in HU rat cerebral and carotid arteries. Vascular contractile and dilate responses were assessed in a myograph organ bath. NOx content in cerebral and carotid arteries was measured. We found enhanced maximal contractile response and impaired endothelium-dependent relaxation in HU rat basilar (P < 0.01) and common carotid artery (P < 0.05); however, chronic treatment of apocynin (50 mg/kg/day) partially reversed abnormal vascular response. Furthermore, 21-day HU increased arterial NOx content (P < 0.01) in cerebral and carotid arteries compared with control rats; however, apocynin treatment restored it toward near-normal values. These data demonstrated that NAD(P)H oxidase-derived oxidative stress mediated abnormal vasoreactivity though nitric oxide mechanism in the settings of simulated microgravity.     

Contractile responsiveness of coronary arteries from exercise-trained rats

Parker, Janet L., Mildred L. Mattox, and M. Harold Laughlin.Contractile responsiveness of coronary arteries from exercise trained rats. J. Appl. Physiol. 83(2):434-443, 1997.The purpose of this study was to determine whetherexercise training alters vasomotor reactivity of rat coronary arteries.In vitro isometric microvessel techniques were used to evaluatevasomotor properties of proximal left anterior artery rings (1 ring peranimal) from exercise-trained rats (ET;n = 10) subjected to a 12-wk treadmill training protocol (32 m/min, 15% incline, 1 h/day, 5 days/wk) andcontrol rats (C; n = 6) restricted tocage activity. No differences in passive length-tension characteristicsor internal diameter (158 ± 9 and 166 ± 9 µm) were observedbetween vessesls of C and ET rats. Concentration-response curves toK⁺ (5-100 mM), prostaglandinF₂(10⁸-10⁴M), and norepinephrine(10⁸-10⁴)were unaltered (P > 0.05) incoronary rings from ET rats compared with C rats; however, lower valuesof the concentration producing 50% of the maximal contractile responsein rings from ET rats (P = 0.05)suggest that contractile sensitivity to norepinephrine wasenhanced. Vasorelaxation responses to sodium nitroprusside (10⁹-10⁴M) and adenosine(10⁹-10⁴M) were not different (P > 0.05)between vessels of C and ET rats. However, relaxation responses to theendothelium-dependent vasodilator acetylcholine (ACh;10¹⁰-10⁴M) were significantly blunted (P < 0.001) in coronary rings from ET animals; maximal ACh relaxationaveraged 90 ± 5 and 46 ± 12%, respectively, in vessels of Cand ET groups. In additional experiments, two coronary rings (proximaland distal) were isolated from each C(n = 7) and ET(n = 7) animal. Proximal coronaryartery rings from ET animals demonstrated decreased relaxationresponses to ACh; however, ACh-mediated relaxation of distal coronaryrings was not different between C and ET groups.N^G-monomethyl-L-arginine(inhibitor of nitric oxide synthase) blocked ACh relaxation of allrings. L-Arginine (substrate fornitric oxide synthase) did not improve the blunted ACh relaxation in proximal coronary artery rings from ET rats. These studies suggest thatexercise-training selectively decreases endothelium-dependent (ACh) butnot endothelium-independent (sodium nitroprusside) relaxation responsesof rat proximal coronary arteries; endothelium-dependent relaxation ofdistal coronary arteries is unaltered by training.

     

Selective mobilization of CD14(+)CD16(+) monocytes by exercise

Strenuous, anaerobic exercise leads to an increaseof leukocytes that are mobilized from the marginal pool. We haveanalyzed in human peripheral blood the effect of exercise on the number of CD14⁺CD16⁺ monocytes as determined bytwo-color immunofluorescence and flow cytometry. We show herein thatthis type of monocyte responds with a dramatic up to 4.8-fold increase.Mobilization does not occur after 1 min at 100 or 200 W but 1 min at400 W leads to a twofold increase of theCD14⁺CD16⁺ monocytes immediately afterexercise. The numbers remain high at 5 min and gradually decrease toreach the initial level at 20 min postexercise. After 20 min of rest,the CD14⁺CD16⁺ monocytes can be mobilized againby a second exercise. The CD14⁺CD16⁺ monocytesappear to be mobilized from the marginal pool where they preferentiallyhome because of a higher expression of adhesion molecules like CD11dand very late antigen-4. Exercise goes along with an increaseof catecholamines, and mobilization of theCD14⁺CD16⁺ monocytes can be substantiallyreduced by treatment of donors with the -adrenergic receptor blockerpropranolol. Mobilization of CD14⁺CD16⁺monocytes by a catecholamine-dependent mechanism may contribute to theincrease of these cells in various clinical conditions.

     

Pulmonary vasoconstrictor effects of prostacyclin in rats: potential role of thromboxane receptors

Zhao, Yi-Ju, Jian Wang, Mary L. Tod, Lewis J. Rubin, andXiao-Jian Yuan. Pulmonary vasoconstrictor effects of prostacyclin in rats: potential role of thromboxane receptors. J. Appl. Physiol. 81(6): 2595-2603, 1996.Endogenousprostacyclin (PGI₂; epoprostenol) is a potent endothelium-derived pulmonary vasodilator. However, theeffects of exogenous PGI₂ onisolated arteries could be either relaxant or contractile, depending onthe species and organ studied. The present study investigated thedistal pathways involved in thePGI₂-induced contraction in ratintrapulmonary artery (PA) and relaxation in lamb PA. When vessels wereprecontracted with 30 mM K⁺,PGI₂ (1 µM) induced relaxationin lamb PA but caused contraction in rat PA. Use of 30 mMK⁺, phenylephrine, serotonin,angiotensin II, or hypoxia to precontract the vessels did not alter thecontractile effect of PGI₂ in rat PA. Nevertheless, PGI₂ produced amild relaxation in rat PA precontracted by U-46619, a thromboxaneA₂(TxA₂)-receptor agonist, whereas the TxA₂-receptor blocker SQ-29548(0.1-0.5 µM) abolished the contractile response in rat PA. Thesedata suggest that PGI₂-induced contraction is mediated by activation ofTxA₂ receptors. ThePGI₂-induced modest relaxation inrat PA, which was only observed whenTxA₂ receptors were blocked bySQ-29548, suggests that thePGI₂-mediated vasorelaxant pathwayis diminished in these vessels. Simultaneous application of forskolin,an adenylate cyclase activator, and rolipram, a phosphodiesteraseinhibitor, caused similar relaxation in both rat and lamb PA. Thissuggests that the adenosine 3,5-cyclic monophosphate-dependent relaxing pathway is intact in rat PA and iscomparable to that in lamb PA. On the basis of these data, we concludethat the pathways responsible for the paradoxical effects ofPGI₂ on rat and lamb PA arelocated upstream of the adenosine 3,5-cyclicmonophosphate-dependent relaxing pathway and that a paucity ofPGI₂ receptors in rat PA may beresponsible.

     

Heat acclimation does not alter rat mesenteric artery response to norepinephrine

Previous studieshave shown that heat acclimation raises the temperature threshold forheat-induced splanchnic vasoconstriction in the rat (W. Haddad and M. Horowitz. Thermal Balance in Health and Disease,Advances in Pharmacological Sciences. Basel:Birkhauser, 1994, p. 203-208; M. Shochina, W. Haddad, U. Meiri,and M. Horo-witz. J. Therm. Biol.21: 289-295, 1996). We tested the hypothesis that heat acclimationalters splanchnic resistance artery sensitivity to norepinephrine (NE).Male Sprague-Dawley rats (n = 5) were acclimated to 35°C ambient temperature for 5-8 wk. Controlrats (n = 5) were maintained at22-23°C ambient temperature for 5-7 wk. Small mesentericartery segments (2- to 3-mm length, 100- to 340-µm ID) were isolated,cannulated at both ends, and pressurized to 50 mmHg. Artery luminaldiameter was measured in response to cumulative doses of NE(10⁹ to10⁵ M) by using videomicroscopy. NE dose response was measured at 37 and 43°C bathtemperatures. There were no differences in constriction responses to NEbetween acclimated and control rat arteries at either 37 or 43°C.We conclude that acclimation does not alter rat mesenteric arterysensitivity to NE.     

Exercise training enhances adrenergic constriction and dilation in the rat spinotrapezius muscle

Treadmill training increases functionalvasodilation in the rat spinotrapezius muscle, although there is noacute increase in blood flow and no increase in oxidative capacity. Toassess concurrent changes in vascular reactivity, we measured arterial diameters in the spinotrapezius muscle of sedentary (Sed) and treadmill-trained (Tr; 9-10 wk; terminal intensity 30 m/min,1.5° incline, for 90 min) rats during iontophoretic application of norepinephrine, epinephrine (Epi), andH⁺ (HCl) and during superfusionwith adenosine. Terminal-feed arteries and first-order arterioles in Trrats constricted more than those in Sed rats at the higher currentdoses of norepinephrine and Epi. In contrast, at low-current doses ofEpi, first- and second-order arterioles dilated in Tr but not in Sedrats. The vascular responses to HCl were highly variable, butsecond-order arterioles of Tr rats constricted more than those of Sedrats at intermediate-current doses. There were no significantdifferences between Sed and Tr rats in the vascular responses toadenosine. Both adrenergic vasodilation and vasoconstriction wereenhanced in the spinotrapezius muscle of Tr rats, and enhancedadrenergic vasodilation may contribute to increased functionalvasodilation. These observations further demonstrate vascularadaptations in "nontrained" skeletal muscle tissues.

     

Effects of hepatic portal infusion of deionized water on metabolic and hormonal responses to exercise in rats

The present study was conducted to investigatethe in vivo effects of an intrahepatic infusion of deionized waterduring exercise in rats. Adrenodemedullated male Sprague-Dawley ratswere continuously infused for 30 min either at rest or during treadmillexercise (26 m/min, 0% grade). Rats were randomly assigned to one ofthree infusion conditions (52 µl/min) with either deionized water(PW) or saline (PS; NaCl; 0.9%) via the hepatic portal vein ordeionized water through the jugular vein (JW). The exercise periodcaused a significant (P < 0.05)decrease in liver glycogen and relative liver water content andperipheral and portal blood glucose and insulin while increasingperipheral and portal glucagon andK⁺ plasma concentrations. Theseresponses, with the exception of K⁺, were not influenced by thedifferent types of infusions. The increase inK⁺ during exercise wassignificantly (P < 0.05) higher inJW rats than in the PW and PS groups. Both the infusion and exerciseprotocols did not significantly alter the liver weight-to-body weightratio, plasma osmolality, free fatty acids, -hydroxybutyrate,Na⁺,Cl, vasopressin, andcatecholamine concentrations. It is concluded that an hepatic portalinfusion of deionized water does not specifically alter the metabolicand hormonal responses to exercise in rats.

     

Vascular wall dysfunction in JCR:LA-cp rats: effects of age and insulin resistance

We tested thehypothesis that aging and insulin resistance interact to increasevascular dysfunction by comparing the function of isolated mesentericresistance arteries in obese, insulin-resistant JCR:LA-cp rats andlean, insulin-sensitive rats of the same strain at 3, 6, 9, and 12 moof age. The peak constrictor responses to norepinephrine,phenylephrine, and high potassium were elevated in arteries from obeserats. Responses to these agents increased with age in both obese andlean rats. An eicosanoid constrictor contributed substantially tovasoconstriction in the arteries from both lean and obese animals.Inhibition of nitric oxide synthase increased the vasoconstrictorresponse to norepinephrine in both obese and lean rats. This effectincreased with age in lean rats only. Vascular relaxation in responseto acetylcholine and sodium nitroprusside was impaired in the obeserats and did not alter with age. The results suggest that obeseJCR:LA-cp rats have enhanced maximal constriction, which originates inthe arterial smooth muscle and increases with age. There is evidencethat the ability of the arteries to compensate for the enhancedcontractility is impaired in obese rats, particularly with advanced age.

     

Acid-base regulation after maximal exercise testing in late gestation

Kemp, Justin G., Felicia A. Greer, and Larry A. Wolfe.Acid-base regulation after maximal exercise testing in late gestation. J. Appl. Physiol. 83(2):644-651, 1997.This study employed Stewart's physicochemicalapproach to quantify the effects of pregnancy and strenuous exercise onthe independent determinants of plasmaH⁺ concentration([H⁺]). Subjects werenine physically active pregnant women [mean gestational age = 33 ± 1 (SE) wk] and 14 age-matched nonpregnant controls. Venousblood samples and respiratory data were obtained at rest and during 15 min of recovery from a maximal cycle ergometer test that involved 20 W/min increases in work rate to exhaustion. Mean values for[H⁺],PCO₂, and total protein increased,whereas those for bicarbonate concentration([HCO₃]) and the strong ion difference ([SID]) decreased in the transition fromrest to maximal exercise within both groups. At rest and throughoutpostexercise recovery, the pregnant group exhibited significantly lowermean values for PCO₂,[HCO₃], and total protein,whereas [SID] was significantly lower at rest and early recovery from exercise.[H⁺] was also lower atall sampling times in the pregnant group, but this effect wassignificant only at rest. Our results support the hypothesis thatreduced PCO₂ and weak acidconcentration are important mechanisms to regulate plasma[H⁺] and to maintain aless acidic plasma environment at rest and after exercise in lategestation compared with the nonpregnant state. These effects areestablished in the resting state and appear to be maintained aftermaximal exertion.

     

Regulation of the epithelial Na+ channel by intracellular Na+

The hypothesis that the intracellularNa⁺ concentration([Na⁺]_i)is a regulator of the epithelialNa⁺ channel (ENaC) was tested withthe Xenopus oocyte expression systemby utilizing a dual-electrode voltage clamp.[Na⁺]_iaveraged 48.1 ± 2.2 meq (n = 27)and was estimated from the amiloride-sensitive reversal potential.[Na⁺]_iwas increased by direct injection of 27.6 nl of 0.25 or 0.5 MNa₂SO₄.Within minutes of injection,[Na⁺]_istabilized and remained elevated at 97.8 ± 6.5 meq(n = 9) and 64.9 ± 4.4 (n = 5) meq 30 min after theinitial injection of 0.5 and 0.25 MNa₂SO₄,respectively. This increase of[Na⁺]_icaused a biphasic inhibition of ENaC currents. In oocytes injected with0.5 MNa₂SO₄(n = 9), a rapid decrease of inwardamiloride-sensitive slope conductance(g_Na) to 0.681 ± 0.030 of control within the first 3 min and a secondary, slowerdecrease to 0.304 ± 0.043 of control at 30 min were observed.Similar but smaller inhibitions were also observed with the injectionof 0.25 MNa₂SO₄.Injection of isotonicK₂SO₄(70 mM) or isotonicK₂SO₄made hypertonic with sucrose (70 mMK₂SO₄-1.2M sucrose) was without effect. Injection of a 0.5 M concentration ofeitherK₂SO₄,N-methyl-D-glucamine (NMDG) sulfate, or 0.75 M NMDG gluconate resulted in a much smaller initial inhibition (<14%) and little or no secondary decrease. Thusincreases of[Na⁺]_ihave multiple specific inhibitory effects on ENaC that can betemporally separated into a rapid phase that was complete within 2-3 min and a delayed slow phase that was observed between 5 and 30 min.

     

Exercise training increases K+-channel contribution to regulation of coronary arterial tone

The present study examined whether regulation ofcoronary tone in conduit arteries (>1.0 mm ID) is altered by exercisetraining. Yucatan miniature swine were treadmill trained for 16-20wk (Ex) and compared with sedentary counterparts (Sed).Endothelium-denuded arterial rings were stretched to optimal length andallowed to equilibrate for 60 min. Inhibition of eitherCa²⁺-activated channels [1mM tetraethylammonium (TEA) or 10 nM iberiotoxin (IBTX)] orvoltage-dependent K⁺ channels[1 mM 4-aminopyridine (4-AP)] significantlyincreased resting tension in both groups; however, the effect of allK⁺-channel blockers was greater inEx. Addition of 1 mM sodium nitroprusside reduced resting tension inboth groups, confirming the presence of active basal tone; however,sodium nitroprusside-sensitive tone was increased approximately twofoldin Ex compared with Sed group. Perforated patch-clamp experiments onisolated smooth muscle cells demonstrated no effect of exercisetraining on whole cell TEA-sensitive, 4-AP-sensitive, or basalK⁺ current. Similarly, whereasTEA, 4-AP, and IBTX all decreased resting membrane potential, there wasno difference in depolarization between groups. The greater effect ofTEA on resting tension in Ex could be mimicked in Sed by addition ofthe Ca²⁺-channel agonist BAY K8644. In conclusion, the greater response toK⁺-channel blockers after exercisetraining is consistent with an increased contribution ofK⁺ channels to regulation of basaltone in conduit coronary arteries. The lack of an effect of training onK⁺ current characteristics ormembrane potential responses in isolated cells suggests that arequisite factor for enhancedK⁺-channel activation in arteriesfrom Ex, possibly stretch, is absent in isolated cells.

     

K+ supplementation increases muscle [Na+-K+-ATPase] and improves extrarenal K+ homeostasis in rats

Bundgaard, Henning, Thomas A. Schmidt, Jim S. Larsen, andKeld Kjeldsen. K⁺supplementation increases muscle[Na⁺-K⁺-ATPase]and improves extrarenal K⁺homeostasis in rats. J. Appl. Physiol.82(4): 1136-1144, 1997.Effects ofK⁺ supplementation (~200 mmolKCl/100 g chow) on plasma K⁺,K⁺ content, andNa⁺-K⁺-adeonsinetriphosphatase(ATPase) concentration([Na⁺-K⁺-ATPase])in skeletal muscles as well as on extrarenalK⁺ clearance were evaluated inrats. After 2 days of K⁺supplementation, hyperkalemia prevailed(K⁺-supplemented vs.weight-matched control animals) [5.1 ± 0.2 (SE) vs. 3.2 ± 0.1 mmol/l, P < 0.05, n = 5-6], and after 4 daysa significant increase in K⁺content was observed in gastrocnemius muscle (104 ± 2 vs. 97 ± 1 µmol/g wet wt, P < 0.05, n = 5-6). After 7 days ofK⁺ supplementation, a significantincrease in[³H]ouabain bindingsite concentration (344 ± 5 vs. 239 ± 8 pmol/g wet wt,P < 0.05, n = 4) was observed in gastrocnemiusmuscle. After 2 wk, increases in plasmaK⁺,K⁺ content, and[³H]ouabain bindingsite concentration in gastrocnemius muscle amounted to 40, 8, and 68%(P < 0.05) above values observed inweight-matched control animals, respectively. The latter change wasconfirmed by K⁺-dependentp-nitrophenyl phosphatase activitymeasurements. Fasting for 1 day reduced plasmaK⁺ andK⁺ content in gastrocnemius musclein rats that had been K⁺supplemented for 2 wk by 3.1 ± 0.3 mmol/l(P < 0.05, n = 5) and 15 ± 2 µmol/g wet wt(P < 0.05, n = 5), respectively. After induction of anesthesia, arterial plasma K⁺was measured during intravenous KCl infusion (0.75 mmolKCl · 100 g bodywt¹ · h¹).The K⁺-supplemented fasted groupdemonstrated a 42% (P < 0.05) lower plasma K⁺ rise, associated with asignificantly higher increase inK⁺ content in gastrocnemius muscleof 7 µmol/g wet wt (P < 0.05, n = 5) compared with their controlanimals. In conclusion, K⁺supplementation increases plasmaK⁺,K⁺ content, and[Na⁺-K⁺-ATPase]in skeletal muscles and improves extrarenalK⁺ clearance capacity.

     

Simulated microgravity upregulates an endothelial vasoconstrictor prostaglandin.

Endothelial nitric oxide contributes to the vascular hyporesponsiveness to norepinephrine (NE) observed in carotid arteries from rats exposed to simulated microgravity. The goal of the present study was to determine whether a cyclooxygenase product of arachidonic acid also influences vascular responsiveness in this setting. Microgravity was simulated in rats by hindlimb unweighting (HU). After 20 days of HU, carotid arteries were isolated from control and HU-treated rats, and vascular rings were mounted in tissue baths for the measurement of isometric contraction. Two cyclooxygenase inhibitors, indomethacin and ibuprofen, and the selective thromboxane A(2) prostanoid-receptor antagonist, SQ-29548, had no effect on the contraction to NE in control vessels but markedly reduced contraction to NE in HU vessels. When the endothelium was removed, indomethacin no longer had any effect on the NE-induced contraction in HU vessels. In endothelium-intact vessels in the presence of indomethacin, the addition of the nitric oxide synthase inhibitor, N(G)-L-nitro-arginine methyl ester, to the medium bathing HU vessels increased the contraction to NE to the level of that of the control vessels. These results indicate that HU treatment induced two endothelial changes in carotid artery that opposed each other. Nitric oxide activity was increased and was responsible for the vascular hyporesponsiveness to NE. The activity of a vasoconstrictor prostaglandin was also increased, and attenuated the vasodilating effect of nitric oxide.     

Simulated microgravity effects on the rat carotid and femoral arteries: role of contractile protein expression and mechanical properties of the vessel wall.

The goal of this study was to determine the effects of microgravity on myofilament protein expression and both passive and active length-force relationships in carotid and femoral arteries. Microgravity was simulated by 20-day hindlimb unweighting (HU) in Wistar male rats, and carotid and femoral artery segments were isolated from both HU and control (CTL) rats for Western blot and length-force analysis. Western blots revealed that HU significantly decreased myosin light chain-20 (MLC-20) protein levels in both carotid and femoral arteries and decreased myosin heavy chain (MHC) in femoral artery. alpha-Actin levels were not altered by HU treatment in either artery. Length-force analysis demonstrated that HU did not change either passive or active length-force relationships in the femoral artery. HU-treated arterial rings developed significantly less force to 100 mM K(+) than CTL, but optimal lengths were identical. In the carotid artery, length-active force curves were identical for both CTL and HU; however the length-passive force curve for HU-treated rings exhibited a steeper slope than CTL, suggesting decreased compliance of the artery wall. In conclusion, our data suggest that the HU-induced decreases in both MLC-20 and MHC in femoral artery are responsible for the decreased contraction to 100 mM K(+) in HU-treated femoral artery rings. In the carotid artery, the HU-induced decrease in vessel wall compliance may counter any decrease in contractility caused by the decreased MLC-20 levels.     

Epidermal growth factor increases lung liquid clearance in rat lungs

Epidermal growthfactor (EGF) has been reported to stimulate the proliferation ofepithelial cells and increase Na⁺flux andNa⁺-K⁺-ATPasefunction in alveolar epithelial cell monolayers. Increases inNa⁺-K⁺-ATPasein alveolar type II cells (AT2) have been associated with increasedactive Na⁺ transport and lungedema clearance across the rat alveolar epithelium in a model ofproliferative lung injury. Thus we tested whether administration ofaerosolized EGF to rat lungs would increase activeNa⁺ transport and lung liquidclearance. Sixteen adult Sprague-Dawley male rats were randomized tothree groups. To a group of six rats, an aerosol generated from 20 µgof EGF in saline was delivered to the lungs, to a second group of fiverats only aerosolized saline was delivered, and a third group of fiverats without treatment served as the control. Forty-eight hourspostaerosolization of rat lungs with EGF there was an ~40% increasein active Na⁺ transport and lungliquid clearance compared with control rats, in the absence of changesin²²Na⁺,[³H]mannitol, andalbumin permeabilities. TheNa⁺-K⁺-ATPaseactivity in AT2 cells harvested from these lungs was increased in ratsthat received aerosolized EGF compared with AT2 cells from both controlrats and rats receiving aerosolized saline. These results support thehypothesis that in vivo delivery of EGF aerosols upregulates alveolarepithelialNa⁺-K⁺-ATPaseand increases lung liquid clearance in rats.