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Blockade of purinergic 2 receptors attenuates the mechanoreceptor component of the exercise pressor reflex

Division of Cardiovascular Medicine, University of California Davis, Davis, California; and Penn State Heart & Vascular Institute, Pennsylvania State University College of Medicine, Hershey, Pennsylvania

Submitted 27 June 2007 ; accepted in final form 28 August 2007

	ABSTRACT

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The finding that pyridoxalphosphate-6-azophenyl-2,4-disulfonic acid (PPADS), a P2 antagonist, attenuated the pressor response to calcaneal tendon stretch, a purely mechanical stimulus, raises the possibility that P2 receptors sensitize mechanoreceptors to static contraction of the triceps surae muscles. The mechanical component of the exercise pressor reflex, which is evoked by static contraction, can be assessed by measuring renal sympathetic nerve activity during the first 2–5 s of this maneuver. During this period of time, group III mechanoreceptors often discharge explosively in response to the sudden tension developed at the onset of contraction. In decerebrated cats, we, therefore, examined the effect of PPADS (10 mg/kg) injected into the popliteal artery on the renal sympathetic and pressor responses to contraction and stretch. We found that PPADS significantly attenuated the renal sympathetic response to contraction, with the effect starting 2 s after its onset and continuing throughout its 60-s period. PPADS also significantly attenuated the renal sympathetic nerve response to stretch, but did so after a latency of 10 s. Our findings lead us to conclude that P2 receptors sensitize group III muscle afferents to contraction. The difference in the onset latency between the PPADS-induced attenuation of the renal sympathetic response to contraction and the renal sympathetic response to stretch is probably due to the sensitivities of different populations of group III afferents to ATP released during contraction and stretch.

group III muscle afferents; group IV muscle afferents; ATP; cats; renal sympathetic nerve activity; neural control of the circulation

The afferent arm of the exercise pressor reflex is comprised of group III fibers, many of which are mechanically sensitive, and group IV fibers, many of which are metabolically sensitive (15, 26). Group IV afferents as well as group III afferents conducting impulses at <4 m/s are stimulated by P2 receptor agonists, whereas group III afferents conducting impulses at 4 m/s or more are not stimulated by these agonists (9, 35). These findings raise the possibility that P2 receptors stimulate metabolically sensitive thin fiber afferents but have no effect on the discharge of mechanically sensitive thin fiber afferents.

Recent studies, however, have shown that PPADS, a P2 receptor antagonist, attenuated the pressor response to stretch, a maneuver that stimulates mechanoreceptors but has little effect on the discharge of metaboreceptors (10). Stretch, however, has been shown to stimulate different populations of group III mechanoreceptors than did static contraction, the stimulus that evokes the exercise pressor reflex (12). Consequently, the finding that PPADS attenuates the pressor response to muscle stretch may not be applicable to the mechanoreceptor component of the exercise pressor reflex.

The mechanical component of the exercise pressor reflex is assessed during the first 2–5 s of static contraction, because group III mechanoreceptors often discharge explosively in response to the sudden tension developed during the first seconds of contraction (15). Moreover, metaboreceptors respond minimally to contraction during the first 2–5 s of its onset (15, 16). Arterial blood pressure is not a useful index of the mechanical component of the exercise pressor reflex because vascular smooth muscle has a slow time constant, making it uncertain whether mechanoreceptors were responsible for any increase in arterial pressure. In contrast, renal sympathetic nerve activity is a useful index of this component because it responds within the first 2–5 s of static contraction (17, 43). In the studies to be described, we have determined the effect of P2 receptor blockade in the triceps surae muscles on the renal sympathetic nerve response to static contraction in decerebrated cats. For purposes of comparison, we have also determined the effect of this blockade on the renal sympathetic nerve response to stretch.

	METHODS

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General. All procedures were reviewed and approved by both the Institutional Care and Use Committees of the University of California, Davis, and the Pennsylvania State University College of Medicine. Adult cats of either sex (n = 15; 3.3 ± 0.5 kg) were initially anesthetized with a mixture of 5% halothane and oxygen. The right jugular vein and common carotid artery were cannulated for the delivery of drugs and fluids and for the measurement of arterial blood pressure, respectively. The carotid arterial catheter was connected to a pressure transducer (model P23 XL, Statham) to monitor blood pressure. Heart rate was calculated beat-to-beat from the arterial pressure pulse by a Gould Biotach amplifier. The trachea was cannulated, and the lungs were ventilated mechanically (Harvard Apparatus). Arterial blood gases and pH were measured by an automated blood gas analyzer (model ABL-700, Radiometer). PCO₂ and arterial pH were maintained within normal range by either adjusting ventilation or intravenous administration of sodium bicarbonate (8.5%). A temperature probe was passed through the mouth to the stomach. Temperature was continuously monitored throughout each experiment and maintained at 37–38°C by a water-perfused heating pad.

The right common iliac artery and vein were isolated, and snares were placed around these vessels to trap the PPADS in the leg (see below). The right triceps surae muscles and tibial nerve were isolated. After the right popliteal artery was isolated for the injection of PPADS, the cat was placed in a Kopf stereotaxic and spinal unit. The calcaneal bone was cut, and its tendon was attached to a force transducer (model FT-10C, Grass) for measurement of the tension developed during stretch and static contraction of the right triceps surae muscles. The knee joint was sutured to a post to secure the right lower limb.

The cats were decerebrated at the mid-collicular level under halothane anesthesia. Just before the decerebration procedure, we tied off the left common carotid artery to reduce bleeding and injected dexamethasone (0.4 mg) intravenously to minimize brain edema. All neural tissue rostral to the mid-collicular section was removed, and the cranial vault was filled with agar. The lungs were then ventilated with room air.

The left renal nerve was exposed using a retroperitoneal approach while the cat was positioned in the Kopf stereotaxic frame and spinal unit. The nerve was suspended in a pool of warm (37°C) mineral oil and then cut; its central end was draped over a monopolar hook electrode attached in series with a high-impedance probe (model HIP 511, Grass) and then amplified (model P511, Grass). Renal sympathetic nerve activity (RSNA) was displayed on a storage oscilloscope (Hewlett-Packard) and made audible. The amplifier was filtered between 100 Hz and 3 kHz.

Experimental protocol. The effect of PPADS (10 mg/ kg) on the reflex pressor, cardioaccelerator, and renal sympathetic responses to static contraction and to stretch of the right triceps surae muscles and calcaneal tendon were determined. Static contraction is a combined mechanical and metabolic stimulus, whereas stretch is a pure mechanical stimulus. Both stimuli were applied for 60 s. Contraction of the triceps surae muscles was induced by electrical stimulation of the right tibial nerve (40 Hz, 25 µs, 1.5–2 times motor threshold); stretch was induced by turning a rack-and-pinion apparatus that was attached to the calcaneal tendon. Baseline tension was set at 0.3–0.5 kg. Attempts were made to match the tension-time index and peak developed tension caused by contraction with those caused by stretch. Arterial blood pressure, heart rate, and RSNA were recorded for 60 s before, during, and after static contraction or tendon stretch. These protocols were repeated 30 min after injection of PPADS (10 mg/ kg) into the right popliteal artery. Immediately before injecting PPADS, we tightened the snare placed around the right common iliac artery and vein. PPADS was then injected into the popliteal artery, and the snares were maintained for 15 min, after which they were released. The hind limb was freely perfused for another 15 min. At this point, the triceps surae muscles were contracted or stretched.

In a second series of experiments using three cats, we examined the possibility that PPADS injected into the popliteal artery circulated to the spinal cord or brain stem to attenuate the pressor and RSNA responses to contraction or stretch. We electrically stimulated (10 Hz; 1 ms; 0.7–1.3 mA; 60 s) the tibial nerve in cats paralyzed with vecuronium bromide (0.5 mg/kg iv) and measured the pressor and RSNA responses before and 30 min after injecting PPADS in the same manner as that described in the experiments in which the triceps surae muscles were either contracted or stretched. The dose of PPADS injected into the popliteal artery has been shown previously to abolish the reflex pressor response to injection of , -methylene ATP injected into the arterial supply of the triceps surae muscles (8). Renal postganglionic sympathetic activity was confirmed by intravenous injection of hexamethonium (10 mg/kg) at the end of data collection in each cat.

Data analysis. Mean arterial blood pressure, heart rate, and RSNA values are expressed as means ± SE. Baseline mean arterial blood pressure and heart rate were measured immediately before a maneuver, and peak mean arterial blood pressure and heart rate were measured during 60 s of tendon stretch and static muscle contraction. RSNA was rectified (Gould) and integrated, and 60-s values were used to compare the differences between baseline and the response to each maneuver. The integrated voltage found after hexamethonium injection was subtracted from the integrated RSNA values. In addition, the time course of the RSNA responses to static contraction and tendon stretch were analyzed at 2 s following the onset of each maneuver and then at each 5-s time point until the maneuver ended. Statistical comparisons were performed either with paired t-tests or two-way repeated-measures ANOVA. If significant main effects were found with an ANOVA, post hoc tests were performed with the Holm-Sidak method to determine significant differences between individual means. The criterion for statistical significance was P < 0.05.

	RESULTS

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PPADS (10 mg/ kg) injected into the popliteal artery attenuated the peak pressor responses to both static contraction and tendon stretch (Fig. 1). Likewise, PPADS attenuated the renal sympathetic nerve responses to both maneuvers when these responses were integrated over their 60-s duration (Fig. 2). Before PPADS injection, the cardioacceleratory responses to either static contraction or tendon stretch were modest, and PPADS injection had no significant effect on them (P > 0.05; Table 1). For both static contraction and tendon stretch, the TTIs were not significantly different from each other (P > 0.05) before and after PPADS injection (Table 2). In every experiment, RSNA was synchronous with the arterial pressure pulse and displayed an expiratory rhythm (Fig. 3). At the end of each experiment, intravenous injection of hexamethonium bromide (20 mg/kg) abolished the activity recorded from each renal nerve, confirming that the activity originated from sympathetic postganglionic fibers.

View larger version (11K): [in this window] [in a new window]   Fig. 1. Effect of pyridoxalphosphate-6-azophenyl-2,4-disulfonic acid (PPADS; 10 mg/kg) on the pressor responses to static contraction (top) and tendon stretch (bottom). Filled bars represent baseline (bs) mean arterial pressure (MAP), and open bars represent peak (pk) MAP in response to either contraction or stretch. Vertical brackets indicate standard errors, and asterisks indicate a significant difference (P < 0.05) between peak value and its corresponding baseline value. Horizontal brackets with asterisks represent significant difference between pressor response to either contraction or stretch before and after PPADS (P < 0.05).

View larger version (10K): [in this window] [in a new window]   Fig. 2. Effect of PPADS (10 mg/kg) on the renal sympathetic nerve responses to static contraction (top) and tendon stretch (bottom). Note that the renal sympathetic responses were integrated over the 60-s period of contraction or stretch. Open bars represent the increase in renal sympathetic nerve activity (RSNA) in response to either contraction or stretch before PPADS, and open bars represent increase in RSNA in response to either contraction or stretch after PPADS. Vertical brackets indicate standard errors, and asterisks indicate a significant difference (P < 0.05) between the increase in RSNA and its corresponding precontraction or prestretch value (P < 0.05). Horizontal brackets with asterisks represent significant difference between increase in RSNA to either contraction or stretch before and after PPADS (P < 0.05).

View larger version (38K): [in this window] [in a new window]   Fig. 3. PPADS (10 mg/kg) attenuates the renal sympathetic and pressor responses to static contraction. A: baseline RSNA and arterial blood pressure (BP) with the triceps surae muscles at rest (before PPADS). B: renal sympathetic and blood pressure responses to static contraction (before PPADS). C: baseline RSNA and arterial blood pressure with the triceps surae muscles at rest (after PPADS). D: renal sympathetic and blood pressure responses to static contraction (after PPADS). Horizontal bar represents 1 s. T, tension developed by the triceps surae muscles.

View larger version (22K): [in this window] [in a new window]   Fig. 4. Time course of the renal sympathetic nerve response to static contraction (top) and tendon stretch (bottom). Note that each maneuver lasted for 60 s. , Mean responses before PPADS (10 mg/kg) was injected into the popliteal artery; , mean responses after PPADS was injected. Vertical brackets are standard errors, and asterisk indicates a significant difference (P < 0.05) between before PPADS and after PPADS. Also note that RSNA is expressed as the percent change from its baseline value. Value at time 0 represents baseline and is expressed as 0% change in RSNA. Note that the first symbol after time 0 represents mean activity 2 s after the start of either static contraction or stretch. Subsequent symbols represent mean activity at 5-s intervals.

	DISCUSSION

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The most important finding from our experiments is that blockade of P2 receptors in skeletal muscle attenuated the rapid renal sympathetic nerve responses to static contraction. Specifically, the attenuation occurred after only 2 s of static contraction, and as a consequence can be attributed to a decrease in group III mechanoreceptor input. From a statistical standpoint, blockade of P2 receptors did not attenuate group III mechanoreceptor input to tendon stretch until the maneuver lasted 10 s. Nevertheless, blockade of P2 receptors did attenuate the overall RSNA response to tendon stretch as well as the responses at all but one time point after 10 s. As with contraction, these effects can only be attributed to a removal of group III mechanoreceptor input.

PPADS infused into the dorsal horn of cats has been shown to attenuate the exercise pressor reflex (6). This finding raised the possibility that, when PPADS was injected into the popliteal artery in our experiments, it traveled to the dorsal horn to exert its effects. To control for this possibility, we stimulated the tibial nerve in paralyzed cats before and after injecting PPADS into the popliteal artery. The injection procedure was identical to that used when the triceps surae muscles were contracted. We found that PPADS injection had no effect on the pressor, cardioaccelerator, or renal sympathetic nerve responses to electrical stimulation of the tibial nerve. These findings suggest that the attenuating effects of PPADS on the pressor and sympathetic responses to contraction and stretch were not caused by circulation of this purinergic antagonist to the spinal cord or brain stem.

The terminals of sympathetic postganglionic fibers (2) and the skeletal muscle cells (19) are the two most likely sources of ATP release in contracting skeletal muscle. Recently, Li et al. (19) found that neuromuscular blockade prevented ATP release into the skeletal muscle interstitium during stimulation of the ventral roots. In contrast, section of the dorsal roots, which prevented the contraction-induced reflex stimulation of sympathetic postganglionic fibers, had no effect on ATP release (19). In addition, Li et al. found that the interstitial concentrations of ATP increased linearly with developed tension in the contracting skeletal muscle.

P2 receptors have two subtypes: the P2X, which is a cation channel, and the P2Y, which is G-protein coupled (3). The available evidence suggests that PPADS does not clearly distinguish between the two P2 receptor subtypes in its blocking activity (18). PPADS, however, does not block P1 receptors (18). We note with interest that the P2X receptor agonist a, methylene ATP stimulated group IV muscle afferents as well as evoked a reflex pressor response when injected into the arterial supply of hind limb muscle (8, 9, 20). Presently, there is no information about the reflex effects evoked by P2Y receptor agonists when injected into the arterial supply of skeletal muscle, although there is a report that the P2Y_2,4 agonist, UTP, stimulated thin-fiber cutaneous afferents (42). Consequently, the relative roles played by P2X and P2Y receptors in evoking the ATP-induced muscle chemoreflex are an unresolved issue.

ATP, lactic acid, bradykinin, and arachidonic acid are produced by contracting skeletal muscle (19, 21, 36, 41). Lactic acid, bradykinin, and cyclooxygenase metabolites of arachidonic acid have been shown to sensitize group III afferents to static contraction and tendon stretch (27, 37, 38). In contrast, information is lacking about whether ATP sensitizes these thinly myelinated muscle afferents to these stimuli. Of interest is the fact that lactic acid, bradykinin, and cyclooxygenase metabolites of arachidonic acid have been found to stimulate directly some group III afferents with conduction velocities in the range of 10–30 m/s (27, 37, 38). In contrast, the ATP analog, , methylene ATP, had no effect on the discharge of group III afferents with conduction velocities over 4 m/s (9). Consequently, if electrophysiological evidence was found that P2 agonists sensitized group III afferents to contraction and stretch, as the reflex evidence suggests is the case, ATP would be the first substance that has this action without also stimulating these thin-fiber afferents when administered exogenously.

The validity of tendon stretch to determine the mechanical component of the exercise pressor reflex is an important issue. Tendon stretch is easy to perform, does not stimulate metabolism in the muscles, and evokes repeatable reflex pressor responses (40) that can be attenuated by gadolinium (11, 25, 39), an agent that blocks mechanogated channels. The problem with tendon stretch is that it does not stimulate the same population of group III muscle afferents as does static contraction (12), which is the defining stimulus for the exercise pressor reflex (30). Specifically, Hayes et al. (12) found that the group III afferents stimulated by tendon stretch conducted impulses, on average, at 16.7 ± 1.5 m/s (n = 14), whereas those stimulated by static contraction conducted impulses, on average at 11.6 ± 1.6 m/s (n = 18; P = 0.03).

Some parallels can be drawn between the responses of golgi tendon organs (i.e., group Ib) and group III afferents to contraction and stretch. Like Golgi tendon organs, some group III afferents respond vigorously to contraction, but only weakly if at all to stretch. Houk and Henneman (14) suggested that contractile elements in muscle, contributing to its elasticity, decreased the tension impinging onto Golgi tendon organs during stretch. This elastic factor was not present during contraction, thereby resulting in this stimulus to be more effective than stretch in stimulating group Ib afferents. If this situation is also found to exist for group III afferents, then the specific response of a group III afferent to contraction and stretch might depend on the orientation of its ending in the contractile elements of the muscle.

The findings by Hayes et al. in cats (12) need to be considered in conjunction with those by Coote and Perez-Gonzalez (4) who, in the same species, found that electrical stimulation of gastrocnemius muscle afferents conducting impulses at 15 m/s or more reflexly decreased sympathetic discharge, whereas electrical stimulation of gastrocnemius afferents conducting impulses at <15 m/s reflexively increased sympathetic discharge (4). The report by Coote and Perez-Gonzalez (4) might provide an electrophysiological basis for the fact that tendon stretch often evokes a smaller pressor response than does static contraction. Specifically, tendon stretch stimulated a population of group III muscle afferents, whose reflex effect was to decrease sympathetic activity; it also had little effect on the discharge of group IV muscle afferents, whose reflex effect was to increase sympathetic activity (15).

Our understanding about the role played by group III mechanoreceptors in the exercise pressor reflex in humans has been evolving. Originally, this role was thought to be small, if not nonexistent, because muscle sympathetic nerve activity did not increase for the first 30 s of static handgrip (24). Subsequently, signal averaging techniques showed that static quadriceps exercise increased muscle sympathetic nerve activity with an onset of only 4–6 s (13), a latency that suggested mechanoreceptor activation. In addition, group III mechanoreceptors have been implicated in the cardioaccelerator and renal vasoconstrictor responses to passive and actual exercise in healthy humans (7, 32–34). Recently, the role played by group III mechanoreceptors in evoking the renal vasoconstrictor component of the exercise pressor reflex has been shown to be even more important in heart failure than in health (28, 29, 31).

In summary, we have presented evidence that ATP release during static contraction plays a role in the reflex stimulation of renal sympathetic component of the exercise pressor reflex. The specific function of the contraction-induced RSNA is not clear and must be defined by measurements of renal function. These measurements should include renal vascular resistance, sodium excretion, and renin production (5).

	GRANTS

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This work was supported by National Institute of Arthritis and Musculoskeletal Diseases Grant no. AR051503.

	ACKNOWLEDGMENTS

 
We thank Yao Dong and Jennifer Probst for technical assistance.

	FOOTNOTES

 

Address for reprint requests and other correspondence: S. G. Hayes, Penn State Heart and Vascular Institute, 500 Univ. Drive, Mail Code H047, Hershey Medical Center, Hershey, PA 17033 (e-mail: shayes1{at}hmc.psu.edu)

The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

	REFERENCES

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1. Burnstock G. A basis for distinguishing two types of purinergic receptors. In: Cell Membrane Receptors for Drugs and Hormones: A Multidisciplinary Approach. New York: Raven, 1978, p. 107–118.
2. Burnstock G. Noradrenaline and ATP: cotransmitters and neuromodulators. J Physiol Pharmacol 46: 365–384, 1995.[Web of Science][Medline]
3. Burnstock G, Kennedy C. Is there a basis for distinguishing two types of P_2-purinoreceptor? Gen Pharmacol 16: 433–440, 1985.[Web of Science][Medline]
4. Coote JH, Pérez-González JF. The response of some sympathetic neurones to volleys in various afferent nerves. J Physiol 208: 261–278, 1970.[Abstract/Free Full Text]
5. DiBona GF, Kopp UC. Neural control of renal function. Physiol Rev 77: 75–197, 1997.[Abstract/Free Full Text]
6. Gao Z, Kehoe V, Sinoway LI, Li J. Spinal P2X receptor modulates reflex pressor response to activation of muscle afferents. Am J Physiol Heart Circ Physiol 288: H2238–H2243, 2005.[Abstract/Free Full Text]
7. Gladwell VF, Coote JH. Heart rate at the onset of muscle contraction and during passive muscle stretch in humans: a role for mechanoreceptors. J Physiol 540: 1095–1102, 2002.[Abstract/Free Full Text]
8. Hanna RL, Hayes SG, Kaufman MP. , -Methylene ATP elicits a reflex pressor response arising from muscle in decerebrate cats. J Appl Physiol 93: 834–841, 2002.[Abstract/Free Full Text]
9. Hanna RL, Kaufman MP. Activation of thin-fiber muscle afferents by a P2X agonist in cats. J Appl Physiol 96: 1166–1169, 2004.[Abstract/Free Full Text]
10. Hanna RL, Kaufman MP. Role played by purinergic receptors on muscle afferents in evoking the exercise pressor reflex. J Appl Physiol 94: 1437–1445, 2003.[Abstract/Free Full Text]
11. Hayes SG, Kaufman MP. Gadolinium attenuates exercise pressor reflex in cats. Am J Physiol Heart Circ Physiol 280: H2153–H2161, 2001.[Abstract/Free Full Text]
12. Hayes SG, Kindig AE, Kaufman MP. Comparison between the effect of static contraction and tendon stretch on the discharge of group III and IV muscle afferents. J Appl Physiol 99: 1891–1896. 2005.[Abstract/Free Full Text]
13. Herr M, Imadojemu V, Kunselman AR, Sinoway LI. Characteristics of the muscle mechanoreflex during quadriceps contraction in humans. J Appl Physiol 86: 767–772, 1999.[Abstract/Free Full Text]
14. Houk J, Henneman E. Responses of Golgi tendon organs to active contractions of the soleus muscle of the cat. J Neurophysiol 30: 466–481, 1967.[Free Full Text]
15. Kaufman MP, Longhurst JC, Rybicki KJ, Wallach JH, Mitchell JH. Effects of static muscular contraction on impulse activity of groups III and IV afferents in cats. J Appl Physiol 55: 105–112, 1983.[Abstract/Free Full Text]
16. Kaufman MP, Rybicki KJ, Waldrop TG, Ordway GA. Effect of ischemia on responses of group III and IV afferents to contraction. J Appl Physiol 57: 644–650, 1984.[Abstract/Free Full Text]
17. Kim JK, Hayes SG, Kindig AE, Kaufman MP. Thin-fiber mechanoreceptors reflexly increase renal sympathetic nerve activity during static contraction. Am J Physiol Heart Circ Physiol 292: H866–H873, 2007.[Abstract/Free Full Text]
18. Lambrecht G. Agonists and antagonists acting at P2X receptors: selectivity profiles and functional implications. Naunyn Schmiedebergs Arch Pharmacol 362: 340–350, 2000.[CrossRef][Web of Science][Medline]
19. Li J, King NC, Sinoway LI. ATP concentrations and muscle tension increase linearly with muscle contraction. J Appl Physiol 95: 577–583, 2003.[Abstract/Free Full Text]
20. Li J, Sinoway LI. ATP stimulates chemically sensitive and sensitizes mechanically sensitive afferents. Am J Physiol Heart Circ Physiol 283: H2636–H2643, 2002.[Abstract/Free Full Text]
21. MacLean DA, La Noue KF, Gray KS, Sinoway LI. Effects of hindlimb contraction on pressor and muscle interstitital metabolite responses in the cat. J Appl Physiol 85: 1583–1592, 1998.[Abstract/Free Full Text]
22. MacLean DA, Saltin B, Radegran G, Sinoway L. Femoral arterial injection of adenosine in humans elevates MSNA via central but not peripheral mechanisms. J Appl Physiol 83: 1045–1053, 1997.[Abstract/Free Full Text]
23. MacLean DA, Vickery LM, Sinoway L. Elevated interstitial adenosine concentrations do not activate the muscle reflex. Am J Physiol Heart Circ Physiol 280: H546–H553, 2001.[Abstract/Free Full Text]
24. Mark AL, Victor RG, Nerhed C, Wallin BG. Microneurographic studies of the mechanisms of sympathetic nerve responses to static exercise in humans. Circ Res 57: 461–469, 1985.[Abstract/Free Full Text]
25. Matsukawa K, Nakamoto T, Inomoto A. Gadolinium does not blunt the cardiovascular responses at the onset of voluntary static exercise in cats: a predominant role of central command. Am J Physiol Heart Circ Physiol 292: H121–H129, 2007.[Abstract/Free Full Text]
26. McCloskey DI, Mitchell JH. Reflex cardiovascular and respiratory responses originating in exercising muscle. J Physiol 224: 173–186, 1972.[Abstract/Free Full Text]
27. Mense S, Meyer H. Bradykinin-induced modulation of the response behaviour of different types of feline group III and IV muscle receptors. J Physiol 398: 49–63, 1988.[Abstract/Free Full Text]
28. Middlekauff HR, Chiu J, Hamilton MA, Fonarow GC, Maclellan WR, Hage A, Moriguchi J, Patel J. Muscle mechanoreceptor sensitivity in heart failure. Am J Physiol Heart Circ Physiol 287: H1937–H1943, 2004.[Abstract/Free Full Text]
29. Middlekauff HR, Niztsche EU, Hoh CK, Hamilton MA, Fonarow GC, Hage A, Moriguchi JD. Exaggerated muscle mechanoreflex control of reflex renal vasoconstriction in heart failure. J Appl Physiol 90: 1714–1719, 2001.[Abstract/Free Full Text]
30. Mitchell JH, Kaufman MP, Iwamoto GA. The exercise pressor reflex: its cardiovascular effects, afferent mechanisms, and central pathways. Annu Rev Physiol 45: 229–242, 1983.[CrossRef][Web of Science][Medline]
31. Momen A, Bower D, Boehmer J, Kunselman AR, Leuenberger UA, Sinoway LI. Renal blood flow in heart failure patients during exercise. Am J Physiol Heart Circ Physiol 287: H2834–H2839, 2004.[Abstract/Free Full Text]
32. Momen A, Leuenberger UA, Ray CA, Cha S, Handly B, Sinoway LI. Renal vascular responses to static handgrip: the role of the muscle mechanoreflex. Am J Physiol Heart Circ Physiol 285: H1247–H1253, 2003.[Abstract/Free Full Text]
33. Momen A, Thomas K, Blaha C, Gahremanpour A, Mansoor A, Leuenberger UA, Sinoway LI. Renal vasoconstrictor responses to static exercise during orthostatic stress in humans: effects of the muscle mechano- and the baroreflexes. J Physiol 573: 819–825, 2006.[Abstract/Free Full Text]
34. Ordway GA, Waldrop TG, Iwamoto GA, Gentile BJ. Hypothalamic influences on cardiovascular response of beagles to dynamic exercise. Am J Physiol Heart Circ Physiol 257: H1247–H1253, 1989.[Abstract/Free Full Text]
35. Reinöhl J, Hoheisel U, Unger T, Mense S. Adenosine triphosphate as a stimulant for nociceptive and non-nociceptive muscle group IV receptors in the rat. Neurosci Lett 338: 25–28, 2003.[CrossRef][Web of Science][Medline]
36. Rotto DM, Massey KD, Burton KP, Kaufman MP. Static contraction increases arachidonic acid levels in gastrocnemius muscles of cats. J Appl Physiol 66: 2721–2724, 1989.[Abstract/Free Full Text]
37. Rotto DM, Schultz HD, Longhurst JC, Kaufman MP. Sensitization of group III muscle afferents to static contraction by products of arachidonic acid metabolism. J Appl Physiol 68: 861–867, 1990.[Abstract/Free Full Text]
38. Sinoway LI, Hill JM, Pickar JG, Kaufman MP. Effects of contraction and lactic acid on the discharge of group III muscle afferents in cats. J Neurophysiol 69: 1053–1059, 1993.[Abstract/Free Full Text]
39. Smith SA, Mitchell JH, Naseem RH, Garry MG. Mechanoreflex mediates the exaggerated exercise pressor reflex in heart failure. Circulation 112: 2293–2300, 2005.[Abstract/Free Full Text]
40. Stebbins CL, Brown B, Levin D, Longhurst JC. Reflex effect of skeletal muscle mechanoreceptor stimulation on the cardiovascular system. J Appl Physiol 65: 1539–1547, 1988.[Abstract/Free Full Text]
41. Stebbins CL, Carretero OA, Mindroiu T, Longhurst JC. Bradykinin release from contracting skeletal muscle of the cat. J Appl Physiol 69: 1225–1230, 1990.[Abstract/Free Full Text]
42. Stucky CL, Medler KA, Molliver DC. The P2Y agonist UTP activates cutaneous afferent fibers. Pain 109: 36–44, 2004.[CrossRef][Web of Science][Medline]
43. Victor RG, Rotto DM, Pryor SL, Kaufman MP. Stimulation of renal sympathetic activity by static contraction: evidence for mechanoreceptor-induced reflexes from skeletal muscle. Circ Res 64: 592–599, 1989.[Abstract/Free Full Text]

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				J. L. McCord, S. G. Hayes, and M. P. Kaufman Acid-sensing ion and epithelial sodium channels do not contribute to the mechanoreceptor component of the exercise pressor reflex Am J Physiol Heart Circ Physiol, September 1, 2008; 295(3): H1017 - H1024. [Abstract] [Full Text] [PDF]

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