Next Article in Journal
Acknowledgment to the Reviewers of Muscles in 2022
Next Article in Special Issue
Pathological Sequelae Associated with Skeletal Muscle Atrophy and Histopathology in G93A*SOD1 Mice
Previous Article in Journal / Special Issue
Muscle Activation during the Squat Performed in Different Ranges of Motion by Women
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Muscles
Volume 2
Issue 1
10.3390/muscles2010003
muscles-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Effects of ATP on Time Parameters of Contractility of Rats’ Slow and Fast Skeletal Muscles in Normal and Hypothermic Conditions

by
Adel E. Khairullin
1,2,*,
Sergey N. Grishin
3,
Azat I. Gabdrahmanov
4 and
Ayrat U. Ziganshin
4
1
Department of Biochemistry, Kazan State Medical University, 420012 Kazan, Russia
2
Research Laboratory of Mechanobiology, Kazan Federal University, 420008 Kazan, Russia
3
Department of Medicinal Physics, Kazan State Medical University, 420012 Kazan, Russia
4
Department of Pharmacology, Kazan State Medical University, 420012 Kazan, Russia
*
Author to whom correspondence should be addressed.
Muscles 2023, 2(1), 23-35; https://doi.org/10.3390/muscles2010003
Submission received: 15 December 2022 / Revised: 8 January 2023 / Accepted: 9 January 2023 / Published: 12 January 2023
(This article belongs to the Special Issue Feature Papers in Muscles)
Browse Figures
Review Reports Versions Notes

Abstract

:
We have previously shown that hypothermia leads to an increase in the synaptic modulating effects of ATP but not of adenosine in several different animal skeletal muscles. In this paper, we studied the effect of ATP on the amplitude–time parameters of single and tetanic contractions of rats’ isolated fast (1) and slow (2) muscles at different temperatures. We found that when muscles were stimulated by the electrical field (0.1 Hz, 0.5 ms, 10 V), with a decrease in the bath temperature from 37 °C to 14 °C (3), there was an increase in the half-relaxation time of the slow muscle (m. soleus), but not of the fast muscle (m. EDL). Similar effects were observed using a carbachol-induced contraction technique, which suggests the postsynaptic (4) nature of the expansion of the contractile response of the slow muscle induced by ATP (5). To confirm the postsynaptic nature of the observed phenomenon, experiments were performed at a high calcium level (7.2 mM), in which the presynaptic effects of ATP were shown to be offset. We found that the hypercalcium condition did not significantly change the effects of ATP on the measured parameters in both muscles. To record muscle tetanic contractions, we gradually increased the frequency of electrical impulses with the increment of 2.5 Hz to achieve the fusion frequencies of 12.5 Hz for m. soleus and 17.5 Hz for m. EDL at normal temperatures. ATP (100 μM) did not change the fusion frequency for both muscles at a normal temperature but decreased this parameter for the slow muscle to 5 Hz at 14 °C without affecting that for the fast muscle. We conclude that ATP potentiates a hypothermia-induced increase in the half-relaxation time of the contraction of rats’ slow, but not fast, skeletal muscles by acting on postsynaptic P2 receptors (6).

1. Introduction

Ambient temperature is constantly changing and affects many body functions [1,2,3,4,5]. The daily fluctuations in the body temperature of warm-blooded animals do not exceed 3 °C (usually 0.5–1.0 °C) [6,7], and the influence of seasonal variation in environmental temperature is largely offset. Maintaining body temperature in certain values provides mammals with the ability to move and perform motor activity in a wide range of environmental temperature conditions [2].
It is known that in the absence of significant temperature fluctuations of internal organs of warm-blooded animals, peripheral parts of their bodies can experience large changes in temperature [8,9]. Thus, the peripheral skeletal muscles retain the ability to contract even when their temperature decreases significantly. According to modern concepts, the strength of skeletal muscle contraction and the rate of contraction and relaxation tend to increase with increasing temperature [10,11,12,13,14]. This was observed, for example, during physical exertion, when an increase in muscle temperature by several degrees was recorded [15,16,17]. However, the above-mentioned works did not pay much attention to the types of skeletal muscles studied. Several types of skeletal muscle fibers are distinguished, of which “slow” and “fast” are mentioned in all classifications [18,19,20]. “Slow” muscles ensure posture maintenance, while “fast” muscles perform fine movements. There is no doubt that these muscles are designed to respond differently to temperature changes, which is observed in practice [1,5,13].
The vertebrate neuromuscular synapse is known to be the best-studied cholinergic synapse. Acetylcholine (ACh) is the main neurotransmitter in the motor unit of the somatic nervous system [21,22,23]. However, embryonic myocytes also initially express receptors to purines, GABA, glutamate and glycine, as well as to ACh; in the process of development the expression of ACh receptors becomes predominant [24,25]. However, the purinergic synaptic modulation remains functionally important [26,27,28].
We have previously shown that in the neuromuscular synapse of frog phasic muscles, ATP inhibits mediator release by activating P2Y12 receptors [29,30,31]. Our further studies covered a wide range of motor unit types of different laboratory animals [32,33,34,35]. We found that the effects of ATP on the amplitude of the contractile responses of different muscles are mostly pronounced under hypothermic conditions. However, a contribution of ATP to the modulation of the temporal parameters of the contractile activity of “slow” and “fast” muscles in rodents under hypothermia has never been reported.

2. Results

2.1. Influence of Temperature on the Time Parameters of Single Contractile Responses of m. soleus and m. EDL Induced by EFS

Averaged over 18 experiments, m. soleus contractions at 37 °C showed the following characteristics: contraction force 2.61 ± 0.07 g, contraction time 0.081 ± 0.008 s, and half-relaxation time 0.092 ± 0.007 s. With a decreasing temperature, there was an increase in both the contraction force and half-relaxation time of m. soleus. Thus, at 14 °C, the m. soleus half-relaxation time reached 0.120 ± 0.009 s (n = 8; p = 0.012; Figure 1A).
At the physiological temperature (37 °C), the contraction force of the m. EDL was 748.3 ± 38.9 mg, the contraction time was 0.057 ± 0.003 s, and the half-relaxation time was 0.067 ± 0.005 s. When the temperature was lowered to 14 °C, the measured parameters did not change significantly (n = 8; Figure 1B).

2.2. Effect of ATP and Suramin on Temporal Parameters of Single Contractile Responses of m. soleus and m. EDL Induced by EFS in Normal and Hypothermic Conditions

ATP at a concentration of 100 μM at 37 °C did not significantly modify the parameters of EFS-evoked contractions of m. soleus: 105.2 ± 4.9% of initial values (n = 18, p = 0.473; Figure 2A) and 102.7 ± 6.1% (n = 18, p = 0.952; Figure 2B) for m. EDL.
When the temperature of the m. soleus incubation solution decreased, the effect of exogenous ATP was manifested by an increase in the half-relaxation time at 14 °C. Thus, at this temperature, the ATP action was 147.9 ± 5.1% (n = 18, p = 0.029, Figure 2A) of the averaged value of this parameter without ATP. The action of ATP on m. EDL with a decrease in temperature to 14 °C was 109.9 ± 4.7% (n = 18, p = 0.637, Figure 2B).
The modulating effect of 100 μM of ATP and temperature on both muscles at each of the temperatures studied was prevented by a non-selective P2 receptor antagonist suramin (100 μM, Figure 2A,B).

2.3. Effect of ATP at High Ca2+ Concentration

When the concentration of extracellular calcium was increased to 7.2 mM, ATP at a concentration of 100 µM at 37 °C did not significantly modify half-relaxation times of m. soleus and m. EDL, which were 105.5 ± 5.1% (n = 14, p = 0.486) and 102.9 ± 5.6% of the baseline values (n = 14, p = 0.759), respectively.
When the temperature decreased, the effect of exogenous ATP was manifested by an increase in m. soleus half-relaxation time. At 14 °C, in the presence of ATP, the half-relaxation time of this muscle was 149.5 ± 5.7% (n = 12, p = 0.022; Figure 3A), compared with the value without ATP at 37 °C. In m. EDL, ATP caused no significant changes: at 14 °C, ATP increased the half-relaxation time to 112.9 ± 4.6% (n = 12, p = 0.824; Figure 3B) of the value of this parameter without ATP at 37 °C. The addition of suramin at a concentration of 100 µM abolished the modulating effects of ATP and temperature in both muscles in each of the temperature regimes studied (Figure 3A,B).

2.4. Effect of ATP on the Tetanic Contractile Responses of m. soleus and m. EDL Evoked by Electrical Stimulation in Normal and Hypothermic Conditions

To record “smooth” tetanic contractions, the electrical pulse frequency was gradually increased, starting from 2.5 Hz with the increment of 2.5 Hz until single contractile responses were obtained (fusion frequency). At a normal temperature, this was observed at a frequency of 12.5 Hz for m. soleus and 17.5 Hz for m. EDL (Figure 4).
In general, ATP and suramin showed effects on the tetanic contractions of both rat skeletal muscles similar to the respective effects of these agents on the force of single-muscle contractions under the same conditions. These data are summarized in Table 1.
A decrease in the bath temperature led to a decrease in the fusion frequency of tetanic muscle contractions in m. soleus, but not in m. EDL (see Table 2). ATP at a concentration of 100 μM further decreased the fusion frequency of tetanic contractions on m. soleus upon hypothermia. However, on m. EDL, these effects were not evident.

2.5. Influence of Temperature on the Timing of Single Contractile Responses of m. soleus and m. EDL Induced by Carbachol

The submaximal concentration of carbachol-induced contractions of the m. soleus was 8 × 10−4 M, and for the rat m. EDL, it was 2 × 10−4 M. We found that at 20 min intervals between contractions, the muscle preparations were able to develop identical isometric contractions throughout the experiment (2–4 h).
At the physiological temperature (37 °C), the contraction parameters of m. soleus averaged over 18 experiments were as follows: contraction force 0.68 ± 0.08 g, contraction time 13.18 ± 0.61 s, and half-relaxation time 15.05 ± 0.74 s. For m. EDL, the contraction force was 187.2 ± 9.9 mg, the contraction time was 8.24 ± 0.43 s, and the half-relaxation time was 11.09 ± 0.68 s. With decreasing temperature, there was an increase in the half-relaxation time of m. soleus; at 14 °C, it was 20.31 ± 0.82 s (n = 10; p = 0.027; Figure 5A). The half-relaxation time of m. EDL did not significantly change with the decreasing temperature and was 12.08 ± 0.71 s at 14 °C (n = 10; p = 0.341; Figure 5B).

2.6. Effect of ATP and Suramin on Temporal Parameters of Single Contractile Responses of m. soleus and m. EDL Induced by Carbachol in Normal and Hypothermic Conditions

ATP at a concentration of 100 μM at 37 °C did not significantly modify the temporal parameters of carbachol-induced contractions of m. soleus: 106.1 ± 5.5% of baseline values (n = 15, p = 0.516; Figure 6A), and 103.8 ± 5.3% (n = 15, p = 0.713; Figure 6B) for m. EDL.
When the temperature of the m. soleus washing solution decreased, the effect of exogenous ATP at a concentration of 100 μM was manifested by an increase in the half-relaxation time at 14 °C. Thus, at this temperature, the action of 100 µM of ATP was 153.9 ± 6.4% (n = 9, p = 0.018, Figure 6A) of the averaged value of this parameter before ATP delivery. The effect of ATP on m. EDL with a decrease in temperature to 14 °C was 113.5 ± 5.3% (n = 9, p = 0.582, Figure 6B).
The modulating effect of ATP and temperature on both muscles at each of the temperature regimes studied was abolished by suramin, a non-selective P2-receptor antagonist (Figure 6A,B).

3. Discussion

It has long been known that a change in temperature has a dramatic effect on the nature of limb muscular activity. One of the earliest available scientific papers on the subject [36] begins with the following phrase: “It is well known that the contractile act is less prolonged in time at higher temperature than at lower temperature, but the effect of temperature on the mechanics of muscle contractility remains unclear”. This question remains almost just as unclear at present [37,38]. At the same time, if a muscle is stimulated directly, a change in temperature does not have such an effect. So, the cause of the discussed phenomenon is synaptic.
It was believed that changes in neuro-muscular conductivity at low temperature can be due to the dysfunction of enzyme systems [39,40] or processes of energy production and transfer [41,42]. However, it was found that the contribution of the temperature sensitivity of metabolic processes in muscle fibers cannot justify huge changes in the character of a contraction of the entire muscle organ during temperature changes [43].
Now, it has become clear that such dramatic changes in contractile responses under hypothermia are due to the involvement of ATP, a modulator of synaptic transmission.
Responses mediated by P2 receptors are temperature-dependent [44,45]. This was first established on smooth muscles [46], and later, on frog skeletal muscles [47].
In comparative experiments involving hypothermia, we further investigated the pre- and postsynaptic effects of ATP on the amplitude parameters of single contractile responses of fast and slow skeletal muscles in warm-blooded animals [31,32,33,34]. In experiments on rat muscles, it was found that ATP has negative presynaptic modulating effects in the neuromuscular junction of fast and slow muscles and postsynaptic effects in fast muscles. As for the postsynaptic effect in slow muscles, a facilitating effect of ATP on the amplitudes of contractile responses was recorded, which was most pronounced under hypothermia conditions (14 °C) [31].
In the experiments presented in this paper, a decrease in temperature led to an increase in the half-relaxation time of the rats’ slow muscle (m. soleus) but not the fast (m. EDL). Carbachol-induced contractions were used to reveal the mechanism, and similar effects were observed, suggesting the postsynaptic nature of the expansion of the contractile response of slow muscles under the influence of ATP.
Although temperature reduction significantly reduces the production of ACh in myoneural synapses, it has been shown on rat diaphragm preparations that contractions of mixed muscles are maintained and facilitated by the inhibition of the enzymatic breakdown of the mediator and the hypersensitivity of postsynaptic cholinoreceptors [48]. Similarly, in our previous experiments on slow muscle preparations, the amplitudes of contractions of rat m. soleus muscles increased during hypothermia, regardless of whether it was caused by the direct (carbachol) or indirect (electrical stimulation) activation of postsynaptic receptors [31]. We hypothesize that these effects are mainly due to the increased sensitivity of nicotinic receptors under hypothermia. A decrease in the activity of the mediator-degrading enzyme is probably less important here, as carbachol is less actively hydrolyzed by cholinesterase.
The nicotinic receptor has been found to contain ATP-binding centers [49,50]. ATP has also been found to increase the open state time and the frequency of opening of ACh-activated ion channels in embryonic muscles [51,52]. There is evidence that ATP may also exhibit a potentiating effect in mature muscles [53,54].
It has also previously been found that the inhibition of acetylcholinesterase slows down the single endplate current, indicating a postsynaptic potentiating effect. In this situation, exogenous ATP acts on current decay similarly to exogenous ACh, which can also cause the deceleration of synaptic signal decay [53].
To record “smooth” tetanic contractions, we increased the frequency of electrical impulses to 12.5 Hz for m. soleus and to 17.5 Hz for m. EDL. ATP at the reference temperatures (37, 26, and 14 °C) was found to show effects on the temporal parameters of tetanic contractions. A decrease in the rate of slow muscle fusion was observed, but not fast muscle fusion in the presence of ATP. To confirm the postsynaptic nature of the observed phenomenon in slow muscle, experiments were performed under conditions of elevated calcium (7.5 mM), which have been shown [29] to offset the presynaptic effects of ATP.
The anterior front of the smooth tetanus of both muscles recorded under in vitro conditions was of a ‘classical’ shape: it had a constant increase in strength around the ‘plateau’ phase [55].
On the other hand, in the series with smooth tetanus of both muscles used, we obtained the effects of purine agents similar to those observed in experiments with single-muscle contractions. This allowed us to fully correlate the results of the key series of experiments on electrically induced single-muscle contractions and carbacholine-induced ‘patterns’ similar in nature to tetanus [55].
We propose that the strong facilitatory postsynaptic effect exhibited by ATP, masking the weaker presynaptic effect, with decreasing temperature, allows the performance of basic locomotion even in animals subjected to deep chilling. There is recently published data on the performance of pronounced movements by the flounder muscle in animals even in the hibernation state, comparable to those observed in active individuals [54].
In the experimental results presented here, suramin prevented all changes in the amplitude–time parameters of the contraction of the rats’ soleus muscles observed during temperature reduction. Thus, neither the strength of contraction nor the time of half-relaxation of the studied muscles changed in the presence of this substance. Suramin eliminated the effect of both ATP itself and, partially, hypothermia. The trypanocidal drug suramin has a wide range of pharmacological effects [56], including the non-selective inhibition of P2 receptors [57] and the suppression of several families of ecto-nucleotidases [58,59]. In our experiments, it not only counteracted the effects of ATP on the contractile parameters of rat muscles but also prevented hypothermia-dependent changes in contractility—regardless of the type of stimulation. This may imply that, as in other organs [60], there is a natural mechanism in warm-blooded skeletal muscles by which P2 receptors mediate temperature changes that become more prominent at low temperatures and which are almost completely inhibited by suramin.
So, why is the post-synaptic effect of ATP on the expansion of the contractile response evident in the synapse of the slow muscle? It is known that the synaptic area is twice as large in the m. soleus than in the m. EDL [61].
The possibility of reciprocal shifts of ion channels floating freely in the lipid phase of the chemoexcitable cell membrane due to the ampere interaction of the currents flowing through them is also known [62]. Although these forces are extremely weak, according to simulations, in the absence of thermal motion and long-term synaptic activity, they could lead to changes in the spatial interposition of ion channels. Ampere forces under hypothermia can initiate the clustering of acetylcholine-activated receptor–channel complexes in regions of the postsynaptic membrane located opposite the active zones of the presynaptic membrane, or in other words, opposite the sites of mediator quantum release. Additionally, it is in the slow muscle that this occurs preferentially in the larger area of the synapse.
Based on the above data, we suggest that the temperature-sensitive tonic effects of endogenous ATP on the force and half-relaxation time of contraction underlie the phenomenology of changes in muscle responses during temperature reduction.

4. Materials and Methods

4.1. Animals and Surgery

The studies were carried out on neuromuscular preparations of white male laboratory rats weighing 140–180 g, which were kept in groups of 3–5 individuals with water and food ad libitum. A total of 108 rats were used in these studies. The animals were anaesthetized via the intraperitoneal administration of sodium ethaminal at a dose of 40 mg/kg, exsanguinated, and m. soleus and m. EDL were isolated on both hind limbs. The isolated muscles were fixed vertically with one end fixed and another attached to a mechanical activity sensor and immersed in 10 mL baths filled with Krebs solution of the following composition (in mM): NaCl 118.0, KCl 4.75, CaCl2 2.5, NaHCO3 24.8, KH2PO4 1.18, MgSO4·7H2O 1.18, glucose 11, pH = 7.4, t = 37 ± 0.5 °C. The thermostat maintained the set point temperature. Muscles were strained with an initial load of 1 g, then left at rest for 30 min to get used to the environmental condition.

4.2. Single Contractions Induced by Electrical Field Stimulation

Electrical field stimulation (EFS) was performed by stimulating the nerve stump, which was placed in a suction-electrode of the original design. A Digitimer MultiStim D330 stimulator (UK) was used for stimulation. Muscle contractions were induced by stimulation with rectangular pulses of 0.1 Hz frequencies, 0.5 ms lengths, and 10 V amplitudes for 2 min. The contraction parameters were recorded with a Linton FSG-01 isometric mechanical activity sensor (UK), and the analog signal was digitized and processed using a Biopack MP100WSW data acquisition system (USA). The average value of parameters of all contractions obtained during 2 min (12 responses) was processed as one result. Parameters of contractile responses were calculated in % relative to initial results obtained at the beginning of the experiment.
After 30 min of tissue fixation, control stimulation of the muscle was performed twice at 5 min intervals, and after ensuring the stability of the contractile responses, experimental procedures were started.
After the initial control responses of the muscle were recorded, ATP (100 µM) was added to a bath, and the contractile responses of the muscle induced by EFS were evaluated after 10 min. After washout, the tissue was incubated with suramin (100 µM) for 20 min, followed by the addition of ATP (100 µM) for 10 min, and the contractile responses were recorded again.
The contractile properties of isolated neuromuscular preparations were studied according to three parameters, which allowed a sufficiently complete reflection of the functional activity of the studied skeletal muscles: contraction time, half-relaxation time (both in seconds), and contraction force (in g), which were determined by analyzing the contraction curve of the studied muscle (Figure 7).

4.3. Contractions Induced by High-Frequency Electrical Field Stimulation

To record “smooth” tetanic contractions, the frequency of EFS impulses was gradually increased with the increment of 2.5 Hz to achieve the fusion frequency. Muscle stimulation was performed in short bursts of pulses for 7 s. At these frequencies, single-muscle contractions of the corresponding muscles were not distinguished, i.e., “smooth” tetanus was observed [54]. The mean value of the contraction force was defined as the average amplitude point of the plateau phase in 2 min, and the force of the contraction was determined in milligrams. All data obtained were calculated in % relative to the initial results obtained at the beginning of the experiment at 37 °C.
In the control experiments, the tissue was incubated with suramin (100 µM) for 20 min, and the muscle responses to EFS were recorded. In each series of the experiments, the effects of the agonists and antagonists were also evaluated in the presence of d-tubocurarine, a nicotinic cholinoblocker, at a concentration of 10 µM.

4.4. Carbachol-Induced Contractions

The contractile responses were induced by adding submaximal concentrations of carbachol to the bath. Experiments were carried out to determine the concentration dependence of carbachol on the test tissue. The submaximal concentration of carbachol was calculated to give 70% of the maximum possible contraction force (usually 3–10 µM). Based on the experiments performed, contractile characteristics (contraction force, contraction time, and half-relaxation time) were obtained under different temperature conditions in the presence of ATP (100 µM) and suramin (100 µM). The mean value of contraction force was treated as a single measurement.

4.5. Assessment of the Temperature Dependency of Rat Skeletal Muscle Contraction

The effect of temperature on the contraction parameters of m. soleus and m. EDL was evaluated in experiments with both EFS and carbachol application initially at 37 °C. The temperature was then decreased to 26 °C and 14 °C. At each temperature condition, ATP (100 M) was applied, and the contractile responses of the muscle were evaluated after 10 min of application. The tissue was then incubated with suramin (100 µM) for 20 min, followed by the addition of ATP (100 µM). The temperature of the solution was controlled with a TE-8A water pump (Techne, UK), and a rapid decrease in the temperature of the liquid in the water pump was performed by adding ice.

4.6. Experiments in Hypercalcium Environment

In separate series of the experiments with EFS, the muscle responses to ATP and suramin at different temperature conditions were recorded first in normal Krebs solution and then in a solution with an elevated calcium ion concentration, 7.2 mM.

4.7. Data Analysis

Mechano-myographic experiments on m. soleus and m. EDL rats were analyzed using ANOVA. A P level of less than 0.05 was taken as significant. Experimental data are presented as mean ± standard error of the mean (n is the number of neuromuscular preparations for the mechano-miographic experiments).

Author Contributions

Conceptualization, A.E.K. and S.N.G.; methodology, A.E.K.; software, A.I.G.; validation, A.E.K. and A.I.G.; formal analysis, A.U.Z.; investigation, A.E.K.; resources, A.U.Z.; data curation, A.I.G.; writing—original draft preparation, A.E.K. and S.N.G.; writing—review and editing, A.U.Z.; visualization, A.E.K.; supervision, A.U.Z.; project administration, A.U.Z.; funding acquisition, A.U.Z. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Kazan State Medical University, grant number 2/22-5; partly funded by Kazan Federal University Strategic Academic Leadership Program (PRIORITY-2030).

Institutional Review Board Statement

The animal study protocol was approved by the Ethics Committee of Kazan State Medical University (protocol code 106/4, from 14 December 2021).

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Angilletta, M.J., Jr. Thermal adaptation. In A Theoretical and Empirical Synthesis; Oxford University Press: Oxford, UK, 2009. [Google Scholar]
  2. James, R.S. A review of the thermal sensitivity of the mechanics of vertebrate skeletal muscle. J. Comp. Physiol. B 2013, 183, 723–733. [Google Scholar] [CrossRef]
  3. Castellani, J.W.; Tipton, M.J. Cold Stress Effects on Exposure Tolerance and Exercise Performance. Compr. Physiol. 2015, 6, 443–469. [Google Scholar] [PubMed]
  4. Bennett, A.F. Thermal dependence of locomotor capacity. Am. J. Physiol. 1990, 259, 253–258. [Google Scholar] [CrossRef] [PubMed]
  5. Racinais, S.; Oksa, J. Temperature and neuromuscular function. Scand. J. Med. Sci. Sport. 2010, 20, 1–18. [Google Scholar] [CrossRef]
  6. Refinetti, R. Amplitude of the daily rhythm of body temperature in eleven mammalian species. J. Therm. Biol. 1999, 24, 477–481. [Google Scholar] [CrossRef]
  7. Wooden, K.M.; Walsberg, G.E. Body temperature and locomotor capacity in a heterothermic rodent. J. Exp. Biol. 2004, 207, 41–46. [Google Scholar] [CrossRef] [Green Version]
  8. Ducharme, M.B.; Van Helder, W.P.; Radomski, M.W. Tissue temperature profile in the human forearm during thermal stress at thermal stability. J. Appl. Physiol. 1991, 71, 1973–1978. [Google Scholar] [CrossRef]
  9. Ranatunga, K.W. Temperature dependence of mechanical power output in mammalian skeletal muscle. Exp. Physiol. 1998, 83, 371–376. [Google Scholar] [CrossRef] [Green Version]
  10. Bennett, A.F. Thermal dependence of muscle function. Am. J. Physiol. 1984, 247, 217–229. [Google Scholar] [CrossRef] [Green Version]
  11. Rall, J.A.; Woledge, R.C. Influence of temperature on mechanics and energetics of muscle contraction. Am. J. Physiol. 1990, 259, 197–203. [Google Scholar] [CrossRef]
  12. Marsh, R.L. Jumping ability of anurans. In Comparative Vertebrate Exercise Physiology; Jones, J.H., Ed.; Academic Press: San Diego, CA, USA, 1994; pp. 51–111. [Google Scholar]
  13. Syme, D.A. Functional properties of skeletal muscle. In Fish Physiology: Fish Biomechanics, Series; Shadwick, R.E., Lauder, G.V., Randall, D.J., Farrell, A.P., Eds.; Academic Press: Cambridge, MA, USA; Elsevier: Amsterdam, The Netherlands, 2006; Volume 23, pp. 179–240. [Google Scholar]
  14. Seebacher, F.; James, R.S. Plasticity of muscle function in a thermoregulating ectotherm (Crocodylusporosus): Biomechanics and metabolism. Am. J. Physiol. 2008, 294, 1024–1032. [Google Scholar]
  15. Saltin, B.; Gagge, A.P.; Stolwijk, J.A. Muscle temperature during submaximal exercise in man. J. Appl. Physiol. 1968, 25, 679–688. [Google Scholar] [CrossRef] [PubMed]
  16. Kenny, G.P.; Reardon, F.D.; Zaleski, W.; Reardon, M.L.; Haman, F.; Ducharm, M.B. Muscle temperature transients before, during, and after exercise measured using an intramuscular multisensor probe. J. Appl. Physiol. 2003, 94, 2350–2357. [Google Scholar] [CrossRef] [Green Version]
  17. Yaicharoen, P.; Wallman, K.; Morton, A.; Bishop, D. The effect of warm-up on intermittent sprint performance and selected thermoregulatory parameters. J. Sci. Med. Sport. 2012, 15, 451–456. [Google Scholar] [CrossRef]
  18. Huxley, A.F. Muscle. Annu. Rev. Physiol. 1964, 26, 131–152. [Google Scholar] [CrossRef]
  19. Rowlerson, A.M.; Spurway, N.C. Histochemical and immunohistochemical properties of skeletal muscle fibres from Rana and Xenopus. Histochem. J. 1988, 20, 657–673. [Google Scholar] [CrossRef]
  20. Grishin, S.N.; Ziganshin, A.U. Synaptic organization of tonic motor units in vertebrates. Biochem. Mosc. Suppl. Ser. A Membr. Cell Biol. 2015, 9, 13–20. [Google Scholar] [CrossRef]
  21. Jimsheleishvili, S.; Marwaha, K.; Sherman, A.l. Physiology, Neuromuscular Transmission; StatPearls Publishing: Treasure Island, FL, USA, 2020. [Google Scholar]
  22. Mukund, K.; Subramaniam, S. Skeletal muscle: A review of molecular structure and function, in health and disease. Wiley Interdiscip. Rev. Syst. Biol. Med. 2020, 12, 1462. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Pasnoor, M.; Dimachkie, M.M. Approach to Muscle and Neuromuscular Junction Disorders. Continuum 2019, 25, 1536–1563. [Google Scholar] [CrossRef]
  24. Apergis-Schoute, J.; Burnstock, G.; Nusbaum, M.P.; Parker, D.; Morales, M.A.; Trudeau, L.E.; Svensson, E. Editorial: Neuronal Ca-transmission. Front. Neural. Circuits 2019, 13, 19. [Google Scholar] [CrossRef]
  25. Svensson, E.; Apergis-Schoute, J.; Burnstock, G.; Nusbaum, M.P.; Parker, D.; Schiöth, H.B. General principles of neuronal co-transmission: Insights from multiple model systems. Front. Neural. Circuits 2019, 21, 117. [Google Scholar] [CrossRef] [PubMed]
  26. Burnstock, G.; Dale, N. Purinergic signalling during development and ageing. Purinergic. Signal 2015, 11, 277–305. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Fulle, S. Purinergic signalling during myogenesis: A role for adenosine and its receptors. Acta Physiol. 2015, 214, 436–439. [Google Scholar] [CrossRef]
  28. Sokolova, E.M.; Grishin, S.N.; Shakirzyanova, A.V.; Talantova, M.V.; Giniatullin, R.A. Distinct receptors and different transduction mechanisms for ATP and adenosine at the frog motor nerve endings. Eur. J. Neurosci. 2003, 18, 1254–1264. [Google Scholar] [CrossRef]
  29. Burnstock, G.; Arnett, T.R.; Orriss, I.R. Purinergic signalling in the musculoskeletal system. Purinergic. Signal 2013, 9, 541–572. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  30. Grishin, S.; Shakirzyanova, A.; Giniatullin, A.; Afzalov, R.; Giniatullin, R. Mechanisms of ATP action on motor nerve terminals at the frog neuromuscular junction. Eur. J. Neurosci. 2005, 21, 1271–1279. [Google Scholar] [CrossRef]
  31. Grishin, S.N.; Ziganshin, A.U. The role of purines in neuromuscular transmission. Biol. Membr. 2013, 30, 243–252. [Google Scholar]
  32. Ziganshin, A.U.; Khairullin, A.E.; Zobov, V.V.; Ziganshina, L.E.; Gabdrakhmanov, A.I.; Ziganshin, B.A.; Grishin, S.N. Effects of ATP and adenosine on contraction amplitude of rat soleus muscle at different temperatures. Muscle Nerve 2017, 55, 417–423. [Google Scholar] [CrossRef]
  33. Ziganshin, A.U.; Khairullin, A.E.; Teplov, A.Y.; Gabdrakhmanov, A.I.; Ziganshina, L.E.; Hoyle, C.H.V.; Ziganshin, B.A.; Grishin, S.N. The effects of ATP on the contractions of rat and mouse fast skeletal muscle. Muscle Nerve 2019, 59, 509–516. [Google Scholar] [CrossRef] [PubMed]
  34. Khairullin, A.E.; Teplov, A.Y.; Grishin, S.N.; Farkhutdinov, A.M.; Ziganshin, A.U. The thermal sensitivity of purinergic modulation of contractile activity of locomotor and respiratory muscles in mice. Biophysics 2019, 64, 812–817. [Google Scholar] [CrossRef]
  35. Khairullin, A.E.; Ziganshin, A.U.; Grishin, S.N. Effect of hypothermia on purinergic synaptic modulation in the rat diaphragm. Biophysics 2020, 65, 1003–1008. [Google Scholar] [CrossRef]
  36. Rutkove, S.B.; Kothari, M.J.; Shefner, J.M. Nerve, muscle, and neuromuscular junction electrophysiology at high temperature. Muscle Nerve 1997, 20, 431–436. [Google Scholar] [CrossRef]
  37. Ferretti, G. Cold and muscle performance. Int. J. Sport. Med. 1992, 1, 185–187. [Google Scholar] [CrossRef]
  38. Cowan, K.J.; Storey, K.B. Freeze-thaw effects on metabolic enzymes in wood frog organs. Cryobiology 2001, 43, 32–45. [Google Scholar] [CrossRef]
  39. MacDonald, J.A.; Storey, K.B. Protein phosphatase type-1 from skeletal muscle of the freeze-tolerant wood frog. Comp. Biochem. Physiol. B Biochem. Mol. Biol. 2002, 131, 27–36. [Google Scholar] [CrossRef]
  40. Boutilier, R.G.; St-Pierre, J. Adaptive plasticity of skeletal muscle energetics in hibernating frogs: Mitochondrial proton leak during metabolic depression. J. Exp. Biol. 2002, 15, 2287–2296. [Google Scholar] [CrossRef] [PubMed]
  41. Mantovani, M.; Heglund, N.C.; Cavagna, G.A. Energy transfer during stress relaxation of contracting frog muscle fibres. J. Physiol. 2001, 537, 923–939. [Google Scholar] [CrossRef]
  42. Nyitrai, M.; Rossi, R.; Adamek, N.; Pellegrino, M.A.; Bottinelli, R.; Geeves, M.A. What limits the velocity of fast-skeletal muscle contraction in mammals? J. Mol. Biol. 2006, 355, 432–442. [Google Scholar] [CrossRef]
  43. Saitongdee, P.; Becker, D.L.; Milner, P.; Knight, G.E.; Burnstock, G. Levels of gap junction proteins in coronary arterioles and aorta of hamsters exposed to the cold and during hibernation and arousal. J. Histochem. Cytochem. 2004, 52, 603–615. [Google Scholar] [CrossRef] [Green Version]
  44. Wallace, A.; Knight, G.E.; Cowen, T.; Burnstock, G. Changes in purinergicsignalling in developing and ageing rat tail artery: Importance for temperature control. Neuropharmacology 2006, 50, 191–208. [Google Scholar] [CrossRef]
  45. Ziganshin, A.U.; Rychkov, A.V.; Ziganshina, L.E.; Burnstock, G. Temperature dependency of P2 receptor-mediated responses. Eur. J. Pharmacol. 2002, 456, 107–114. [Google Scholar] [CrossRef] [PubMed]
  46. Ziganshin, A.U.; Kamaliev, R.R.; Grishin, S.N.; Ziganshina, L.E.; Zefirov, A.L.; Burnstock, G. The influence of hypothermia on P2 receptor-mediated responses of frog skeletal muscle. Eur. J. Pharmacol. 2005, 21, 187–193. [Google Scholar] [CrossRef]
  47. Foldes, F.F.; Kuze, S.; Vizi, E.S.; Deery, A. The influence of temperature on neuromuscular performance. J. Neural. Transm. 1978, 43, 27–45. [Google Scholar] [CrossRef] [PubMed]
  48. Carlson, B.J.; Raftery, M.A. Specific binding of ATP to extracellular sites on Torpedo acetylcholine receptor. Biochem 1993, 32, 7329–7333. [Google Scholar] [CrossRef] [PubMed]
  49. Giniatullin, R.A.; Sokolova, E.M. Modulating role of ATP in the neuromuscular junction. Russ. J. Physiol. 1998, 84, 1132–1138. [Google Scholar]
  50. Fu, W.M. Potentiation by ATP of the postsynaptic acetylcholine response at developing neuromuscular synapses in Xenopus cell cultures. J. Physiol. 1994, 477, 449–458. [Google Scholar] [CrossRef]
  51. Fu, W.M. Regulatory role of ATP at developing neuromuscular junctions. Prog. Neurobiol 1995, 47, 31–44. [Google Scholar] [CrossRef]
  52. Lu, Z.; Smith, D.O. Adenosine 5′-triphosphate increases acetyltholine channel-opening frequency in rat skeletal muscle. J. Physiol. 1991, 436, 45–56. [Google Scholar] [CrossRef]
  53. Ziganshin, A.U.; Khairullin, A.E.; Hoyle, C.H.V.; Grishin, S.N. Modulatory Roles of ATP and Adenosine in Cholinergic Neuromuscular Transmission. Int. J. Mol. Sci. 2020, 21, 6423. [Google Scholar] [CrossRef]
  54. Riley, D.A.; Van Dyke, J.M.; Vogel, V.; Curry, B.D.; Bain, J.L.W.; Schuett, R.; Costill, D.L.; Trappe, T.; Minchev, K.; Trappe, S. Soleus muscle stability in wild hibernating black bears. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2018, 315, 369–379. [Google Scholar] [CrossRef] [Green Version]
  55. Eshpay, R.A.; Khairullin, A.E.; Karimova, R.G.; Nurieva, L.R.; Rizvanov, A.A.; Mukhamedyarov, M.A.; Ziganshin, A.U.; Grishin, S.N. Parameters of single and summated contractions of skeletal muscles in vivo and in vitro. Genes Cells 2015, 10, 123–126. [Google Scholar]
  56. McGeary, R.P.; Bennett, A.J.; Tran, Q.B.; Cosgrove, K.L.; Ross, B.P. Suramin: Clinical uses and structure-activity relationships. Mini Rev. Med. Chem. 2008, 8, 1384–1394. [Google Scholar] [CrossRef] [PubMed]
  57. Lambrecht, G.; Braun, K.; Damer, M.; Ganso, M.; Hildebrandt, C.; Ullmann, H.; Kassack, M.U.; Nickel, P. Structure-activity relationships of suramin and pyridoxal-5′-phosphate derivatives as P2 receptor antagonists. Curr. Pharm. Des. 2002, 8, 2371–2399. [Google Scholar] [CrossRef] [PubMed]
  58. Savegnago, L.; Nogueira, C.W.; Fachinetto, R.; Rocha, J.B. Characterization of ATP and ADP hydrolysis activity in rat gastric mucosa. Cell Biol. Int. 2005, 29, 559–566. [Google Scholar] [CrossRef] [PubMed]
  59. Kiffer-Moreira, T.; Fernandes Sampaio, M.E.; Alviano, D.S.; Axelband, F.; Cesar, G.V.; Cosentino-Gomes, D.; Rodrigues, M.L.; Nimrichter, L.; Vieyra, A.; Alviano, C.S.; et al. Biochemical characterization of an ecto-ATP diphosphohydrolase activity in Candida parapsilosis and its possible role in adenosine acquisition and pathogenesis. FEMS Yeast Res. 2010, 10, 735–746. [Google Scholar] [CrossRef] [Green Version]
  60. Salgado, A.I.; Cunha, R.A.; Ribeiro, J.A. Facilitation by P(2) receptor activation of acetylcholine release from rat motor nerve terminals: Interaction with presynaptic nicotinic receptors. Brain Res. 2000, 877, 245–250. [Google Scholar] [CrossRef]
  61. Fahim, M.A.; Holley, J.A.; Robbins, N. Topographic comparison of neuromuscular junctions in mouse slow and fast twitch muscles. Neuroscience 1984, 13, 227–235. [Google Scholar] [CrossRef]
  62. Larionov, I.; Larionov, A.L.; Nikolsky, E.E. Can the ampere forces be a factor of the ion channels’ lateral mobility? Mathematical modeling. Biol. Membr. 2018, 35, 3–15. [Google Scholar]
Muscles 02 00003 g001 550
Figure 1. Records of single contractile responses of rat m. soleus (A) and m. EDL (B) induced by electrical field stimulation at different temperatures.
Figure 1. Records of single contractile responses of rat m. soleus (A) and m. EDL (B) induced by electrical field stimulation at different temperatures.
Muscles 02 00003 g001
Muscles 02 00003 g002 550
Figure 2. Effect of ATP (100 µM) and suramin (100 µM) on the half-relaxation time of m. soleus (A) and m. EDL (B) at different temperature regimes (n = 12–18). # p < 0.05 from the effect at 37 °C, * p < 0.05 from control.
Figure 2. Effect of ATP (100 µM) and suramin (100 µM) on the half-relaxation time of m. soleus (A) and m. EDL (B) at different temperature regimes (n = 12–18). # p < 0.05 from the effect at 37 °C, * p < 0.05 from control.
Muscles 02 00003 g002
Muscles 02 00003 g003 550
Figure 3. Effects of ATP (100 µM) and suramin (100 µM) on the half-relaxation time of electrical-stimulation-induced contraction of m. soleus (A) and m. EDL (B) at an elevated Ca2+ concentration (7.2 mM) under different temperature regimes. n = 8–14. # p < 0.05 from the effect at 37 °C, * p < 0.05 from control.
Figure 3. Effects of ATP (100 µM) and suramin (100 µM) on the half-relaxation time of electrical-stimulation-induced contraction of m. soleus (A) and m. EDL (B) at an elevated Ca2+ concentration (7.2 mM) under different temperature regimes. n = 8–14. # p < 0.05 from the effect at 37 °C, * p < 0.05 from control.
Muscles 02 00003 g003
Muscles 02 00003 g004 550
Figure 4. Records of contractions of m. soleus (A) and m. EDL (B) at different stimulation frequencies at 37 °C.
Figure 4. Records of contractions of m. soleus (A) and m. EDL (B) at different stimulation frequencies at 37 °C.
Muscles 02 00003 g004
Muscles 02 00003 g005 550
Figure 5. View of single contractile responses of m. soleus (A) and m. EDL (B) induced by carbachol stimulation at different temperatures.
Figure 5. View of single contractile responses of m. soleus (A) and m. EDL (B) induced by carbachol stimulation at different temperatures.
Muscles 02 00003 g005
Muscles 02 00003 g006 550
Figure 6. Effect of ATP on the half-relaxation time of m. soleus (A) and m. EDL (B) induced by carbachol under different temperature regimes. n = 9- 15. # p < 0.05 from the effect at 37 °C, * p < 0.05 from the control.
Figure 6. Effect of ATP on the half-relaxation time of m. soleus (A) and m. EDL (B) induced by carbachol under different temperature regimes. n = 9- 15. # p < 0.05 from the effect at 37 °C, * p < 0.05 from the control.
Muscles 02 00003 g006
Muscles 02 00003 g007 550
Figure 7. Schematic diagram of recording contractile parameters. CF—contraction force, LP—latency period, CT—contraction time, RT—relaxation time, RT/2—half-relaxation time.
Figure 7. Schematic diagram of recording contractile parameters. CF—contraction force, LP—latency period, CT—contraction time, RT—relaxation time, RT/2—half-relaxation time.
Muscles 02 00003 g007
Table
Table 1. Effect of ATP (100 µM) and suramin (100 µM) on the contraction force of the tetanic contraction (in %) of m. soleus (A) and m. EDL (B) under different temperature regimes (n = 8). * p < 0.05 from the effect at 37 °C, # p < 0.05 from control).
Table 1. Effect of ATP (100 µM) and suramin (100 µM) on the contraction force of the tetanic contraction (in %) of m. soleus (A) and m. EDL (B) under different temperature regimes (n = 8). * p < 0.05 from the effect at 37 °C, # p < 0.05 from control).
MusclesSubstancesTemperature
37 °C26 °C14 °C
m. soleusControl100112 ± 7.1153 ± 5.9 *
ATP69 ± 8.0 #82 ± 7.7 #157 ± 9.5 *
suramin + ATP103 ± 5.795 ± 6.4107 ± 6.8 #
m. EDLControl10079 ± 5.864 ± 7.2 *
ATP86 ± 5.5 #58 ± 7.9 #43 ± 6.2 *#
suramin + ATP98 ± 7.197 ± 8.594 ± 9.1 #
Table
Table 2. Effect of temperature on the fusion frequency of tetanic muscle contractions (in Hz) in control and with application of ATP and suramin at a concentration of 100 µM. n = 12.
Table 2. Effect of temperature on the fusion frequency of tetanic muscle contractions (in Hz) in control and with application of ATP and suramin at a concentration of 100 µM. n = 12.
MusclesSubstances37 °C26 °C14 °C
m. soleusControl12.5107.5
ATP12.57.55
suramin12.51010
suramin + ATP12.5107.5
m. EDLControl17.517.515
ATP17.517.515
suramin17.517.515
suramin + ATP17.517.515
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Khairullin, A.E.; Grishin, S.N.; Gabdrahmanov, A.I.; Ziganshin, A.U. Effects of ATP on Time Parameters of Contractility of Rats’ Slow and Fast Skeletal Muscles in Normal and Hypothermic Conditions. Muscles 2023, 2, 23-35. https://doi.org/10.3390/muscles2010003

AMA Style

Khairullin AE, Grishin SN, Gabdrahmanov AI, Ziganshin AU. Effects of ATP on Time Parameters of Contractility of Rats’ Slow and Fast Skeletal Muscles in Normal and Hypothermic Conditions. Muscles. 2023; 2(1):23-35. https://doi.org/10.3390/muscles2010003

Chicago/Turabian Style

Khairullin, Adel E., Sergey N. Grishin, Azat I. Gabdrahmanov, and Ayrat U. Ziganshin. 2023. "Effects of ATP on Time Parameters of Contractility of Rats’ Slow and Fast Skeletal Muscles in Normal and Hypothermic Conditions" Muscles 2, no. 1: 23-35. https://doi.org/10.3390/muscles2010003

Article Metrics

Back to TopTop