Protein differentiation of the superfast swimbladder muscle of the toadfish Opsanus tau

The superfast swimbladder muscle of Opsanus tau differs from the corresponding fast skeletal muscle not only by its well known much more developed sarcoplasmic reticulum but also by its two- to threefold higher parvalbumin contact and a genuine LC₂ myosin light chain.     

The ultrastructure of the swimbladder of the toadfish,Opsanus tau L.

Summary The anterior chamber of the swimbladder of the toadfish Opsanus tau L. is lined by a single layer of columnar gas gland cells, cuboidal cells that resemble gas gland cells but are located outside of the gas gland region, and squamous cells. Multilamellar bodies are numerous in the gas gland cells and the cuboidal cells and are present in smaller numbers in the squamous cells. Capillaries lie in the lamina propria directly below the epithelial lining. A thick continuous muscularis mucosae and a submucosa consisting of tightly packed cells, cell processes, and connective tissue may contribute to the impermeability to gases of the wall of the anterior chamber.The posterior chamber of the swimbladder is lined by a single type of squamous epithelial cell. Multilamellar bodies were occasionally observed in these cells also. Other types of cells frequently form a partial second layer between the epithelial lining and the basement lamina. A thin muscularis mucosae lies directly below the basement lamina and the capillaries of the posterior chamber are located in the submucosa. The tunica externa is a layer of dense connective tissue that surrounds both the anterior and posterior chambers. Collagen fibrils in the form of tactoids are present in this layer.Part of this work was submitted by S.M.M. in partial fulfillment of the requirements for the degree of Doctor of Philosophy, Biology Department, Boston University. S.M.M. is grateful for a National Science Foundation Traineeship.     

Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder

The mating call of the Atlantic toadfish is generated by bursts of high-frequency twitches of the superfast twitch fibers that surround the swimbladder. At 16°C, a calling period can last several hours, with individual 80–100-Hz calls lasting ∼500 ms interleaved with silent periods (intercall intervals) lasting ∼10 s. To understand the intracellular movements of Ca²⁺ during the intercall intervals, superfast fibers were microinjected with fluo-4, a high-affinity fluorescent Ca²⁺ indicator, and stimulated by trains of 40 action potentials at 83 Hz, which mimics fiber activity during calling. The fluo-4 fluorescence signal was measured during and after the stimulus trains; the signal was also simulated with a kinetic model of the underlying myoplasmic Ca²⁺ movements, including the binding and transport of Ca²⁺ by the sarcoplasmic reticulum (SR) Ca²⁺ pumps. The estimated total amount of Ca²⁺ released from the SR during a first stimulus train is ∼6.5 mM (concentration referred to the myoplasmic water volume). At 40 ms after cessation of stimulation, the myoplasmic free Ca²⁺ concentration ([Ca²⁺]) is below the threshold for force generation (∼3 µM), yet the estimated concentration of released Ca²⁺ remaining in the myoplasm (Δ[Ca_M]) is large, ∼5 mM, with ∼80% bound to parvalbumin. At 10 s after stimulation, [Ca²⁺] is ∼90 nM (three times the assumed resting level) and Δ[Ca_M] is ∼1.3 mM, with 97% bound to parvalbumin. Ca²⁺ movements during the intercall interval thus appear to be strongly influenced by (a) the accumulation of Ca²⁺ on parvalbumin and (b) the slow rate of Ca²⁺ pumping that ensues when parvalbumin lowers [Ca²⁺] near the resting level. With repetitive stimulus trains initiated at 10-s intervals, Ca²⁺ release and pumping come quickly into balance as a result of the stability (negative feedback) supplied by the increased rate of Ca²⁺ pumping at higher [Ca²⁺].     

Cytochemical study of the lamellar bodies in the swimbladder of the toadfish Opsanus tau L.

Summary The columnar epithelial cells of the gas gland in the swimbladder of the toadfish, Opsanus tau L., contain lamellar bodies that resemble the lamellar bodies found in epithelial cells of vertebrate lungs. Cytochemical assays indicate that swimbladder lamellar bodies are soluble in chloroform-methanol solution, react with tricomplex flocculation solution (indicating a phospholipid component), exhibit a positive reaction for cholesterol when exposed to digitonin, and contain acid phosphatase.The anterior chamber of the toadfish swimbladder is lined by an extracellular layer. Digitonin-cholesterol crystals are found in this layer when the swimbladder is treated with digitonin. A ruthenium red positive layer is also present in the anterior chamber of the toadfish swimbladder.The structure and cytochemistry of swimbladder lamellar bodies are compared with those of vertebrate lung lamellar bodies. Similarities between the extracellular layer in the swimbladder and the extracellular layer in lungs are also noted.Supported in part by a grant No 1 R23 HL 19593-01 from the National Institutes of Health     

Seasonal variation of sound production in the Lusitanian toadfish Halobatrachus didactylus

Seasonal variation of sound production, which includes boatwhistles, grunts, croaks and double croaks, was studied in the Lusitanian toadfish Halobatrachus didactylus . Boatwhistles were emitted during the mating season in contrast with the other sound types, which were emitted all year round.     

The amino acid sequence of the parvalbumin from the very fast swimbladder muscle of the toadfish (Opsanus tau)

1. The parvalbumin from the very fast striated muscle of the swimbladder of the toadfish (Opsanus tau) has been purified to homogeneity and its amino acid sequence has been completely elucidated. 2. The polypeptide chain is made of 109 residues, belongs to the beta group of parvalbumins and presents characteristics common to many other parvalbumins, i.e. a blocked N-terminal group, a cysteine and an arginine residue at positions 18 and 75 respectively and a quadruplet of acidic residues in the region 59-62.     

Cross-bridge blocker BTS permits direct measurement of SR Ca2+ pump ATP utilization in toadfish swimbladder muscle fibers

Because the major processes involved in muscle contraction require rapid utilization of ATP, measurement of ATP utilization can provide important insights into the mechanisms of contraction. It is necessary, however, to differentiate between the contribution made by cross-bridges and that of the sarcoplasmic reticulum (SR) Ca²⁺ pumps. Specific and potent SR Ca²⁺ pump blockers have been used in skinned fibers to permit direct measurement of cross-bridge ATP utilization. Up to now, there was no analogous cross-bridge blocker. Recently, N-benzyl-p-toluene sulfonamide (BTS) was found to suppress force generation at micromolar concentrations. We tested whether BTS could be used to block cross-bridge ATP utilization, thereby permitting direct measurement of SR Ca²⁺ pump ATP utilization in saponin-skinned fibers. At 25 µM, BTS virtually eliminates force and cross-bridge ATP utilization (both <4% of control value). By taking advantage of the toadfish swimbladder muscle's unique right shift in its force-Ca²⁺ concentration ([Ca²⁺]) relationship, we measured SR Ca²⁺ pump ATP utilization in the presence and absence of BTS. At 25 µM, BTS had no effect on SR pump ATP utilization. Hence, we used BTS to make some of the first direct measurements of ATP utilization of intact SR over a physiological range of [Ca²⁺]at 15°C. Curve fits to SR Ca²⁺ pump ATP utilization vs. pCa indicate that they have much lower Hill coefficients (1.49) than that describing cross-bridge force generation vs. pCa (5). Furthermore, we found that BTS also effectively eliminates force generation in bundles of intact swimbladder muscle, suggesting that it will be an important tool for studying integrated SR function during normal motor behavior. muscle energetics; skinned muscle fibers; sarcoplasmic reticulum calcium ion pumps; cross bridges     

O2-filled swimbladder employs monocarboxylate transporters for the generation of O2 by lactate-induced root effect hemoglobin

The swimbladder volume is regulated by O(2) transfer between the luminal space and the blood In the swimbladder, lactic acid generation by anaerobic glycolysis in the gas gland epithelial cells and its recycling through the rete mirabile bundles of countercurrent capillaries are essential for local blood acidification and oxygen liberation from hemoglobin by the "Root effect." While O(2) generation is critical for fish flotation, the molecular mechanism of the secretion and recycling of lactic acid in this critical process is not clear. To clarify molecules that are involved in the blood acidification and visualize the route of lactic acid movement, we analyzed the expression of 17 members of the H(+)/monocarboxylate transporter (MCT) family in the fugu genome and found that only MCT1b and MCT4b are highly expressed in the fugu swimbladder. Electrophysiological analyses demonstrated that MCT1b is a high-affinity lactate transporter whereas MCT4b is a low-affinity/high-conductance lactate transporter. Immunohistochemistry demonstrated that (i) MCT4b expresses in gas gland cells together with the glycolytic enzyme GAPDH at high level and mediate lactic acid secretion by gas gland cells, and (ii) MCT1b expresses in arterial, but not venous, capillary endothelial cells in rete mirabile and mediates recycling of lactic acid in the rete mirabile by solute-specific transcellular transport. These results clarified the mechanism of the blood acidification in the swimbladder by spatially organized two lactic acid transporters MCT4b and MCT1b.     

Hemodynamics-driven mathematical model of first and second heart sound generation

We propose a novel, two-degree of freedom mathematical model of mechanical vibrations of the heart that generates heart sounds in CircAdapt, a complete real-time model of the cardiovascular system. Heart sounds during rest, exercise, biventricular (BiVHF), left ventricular (LVHF) and right ventricular heart failure (RVHF) were simulated to examine model functionality in various conditions. Simulated and experimental heart sound components showed both qualitative and quantitative agreements in terms of heart sound morphology, frequency, and timing. Rate of left ventricular pressure (LV dp/dt_max) and first heart sound (S1) amplitude were proportional with exercise level. The relation of the second heart sound (S2) amplitude with exercise level was less significant. BiVHF resulted in amplitude reduction of S1. LVHF resulted in reverse splitting of S2 and an amplitude reduction of only the left-sided heart sound components, whereas RVHF resulted in a prolonged splitting of S2 and only a mild amplitude reduction of the right-sided heart sound components. In conclusion, our hemodynamics-driven mathematical model provides fast and realistic simulations of heart sounds under various conditions and may be helpful to find new indicators for diagnosis and prognosis of cardiac diseases.New & noteworthyTo the best of our knowledge, this is the first hemodynamic-based heart sound generation model embedded in a complete real-time computational model of the cardiovascular system. Simulated heart sounds are similar to experimental and clinical measurements, both quantitatively and qualitatively. Our model can be used to investigate the relationships between heart sound acoustic features and hemodynamic factors/anatomical parameters.     

Limits of gas secretion by the salting-out effect in the fish swimbladder rete

Summary The high dissolved gas tensions required for the secretion of gases into deep-sea fish swimbladders are thought to be produced in the rete mirabile by a countercurrent multiplication mechanism, the capacity of which is theoretically limited by the physical characteristics of the rete and by the magnitudes of minute gas solubility changes in the blood plasma. These gas solubility changes are presumably induced through the salting-out effect following the addition of lactic acid to rete venous blood as it circulates through the gas gland. In order to estimate the maximum swimbladder gas pressures attainable by this mechanism, the effects of lactic acid on N₂ and Ar solubilities in water were determined at 5 and 25°C with a new volumetric method. The results show that the salting-out effect with lactic acid is much smaller than with NaCl, and that the agreement between predicted and observed swimbladder gas pressures is more critically dependent on the physical properties of the rete vasculature than indicated by previous theoretical treatments. When augmented by the release of hemoglobin-bound O₂, the salting-out effect with lactic acid appears large enough to account for the production of even the highest swimbladder O₂ pressures, provided the rete characteristics lie within certain reasonable limits. However, successful theoretical explanation of observed swimbladder N₂ pressures in some deep-sea species will require rigorous attention to such theoretically neglected factors as dissolved gas backdiffusion along the rete and the unequal size and number of the rete arterial and venous capillaries.     

Immunoglobulin of the toadfish, Spheroides glaber

The major serum immunoglobulin of the toadfish, Spheroides glaber, was shown to be a tetrameric IgM-like molecule of probable structure (mu2L2)4. The tetrameric molecule could be dissociated, without reduction, into dimeric and monomeric forms. A low molecular weight immunoglobulin present at levels of about one twentieth of those of the high molecular weight IgM was detected in serum.     

New perspectives on mechanisms of sound generation in songbirds

The physical mechanisms of sound generation in the vocal organ, the syrinx, of songbirds have been investigated mostly with indirect methods. Recent direct endoscopic observation identified vibrations of the labia as the principal sound source. This model suggests sound generation in a pulse-tone mechanism similar to human phonation with the labia forming a pneumatic valve. The classical avian model proposed that vibrations of the thin medial tympaniform membranes are the primary sound generating mechanism. As a direct test of these two hypotheses we ablated the medial tympaniform membranes in two species (cardinal and zebra finch) and found that both were still able to phonate and sing without functional membranes. Small changes in song structure (harmonic emphasis, frequency control) occurred after medial tympaniform membrane ablation and suggest that the medial tympaniform membranes play a role in adjusting tension on the labia. Such a role is consistent with the fact that the medial tympaniform membranes are directly attached to the medial labia. There is no experimental support for a third hypothesis, proposing an aerodynamic model for generation of tonal sounds. Indirect tests (song in heliox atmosphere) as well as direct (labial vibration during tonal sound) measurements of syringeal vibrations support a vibration-based sound-generating mechanism even for tonal sounds.     

Sound production evoked by electrical stimulation of the forebrain in the oyster toadfish

In mammals, birds and amphibians the neural pathways controlling sound production descend from higher centers in the forebrain, whereas in fishes only brainstem and spinal centers have been explicitly implicated in sound production. We now report that electrical stimulation of the forebrain of the oyster toadfish (Opsanus tau) readily evokes both the agonistic grunt and the courtship boatwhistle. Boatwhistles are more realistic than ones previously evoked from lower centers. Positive stimulation sites are localized in the preoptic area (nucleus preopticus parvocellularis anterior) and the supracommissural nucleus of the ventral telencephalon, a likely homologue of the amygdala. Both sites contain gonadal steroid-concentrating neurons and play a central role in fish courtship behavior. Evoked sounds form a continuum from knock grunts, burst grunts, transition boatwhistles to complete boatwhistles; sound pressure level (SPL), fundamental frequency and duration increase consistently within the continuum. For all sound types, SPLs exhibit the smallest variation (coefficients of variation of 2.7 to 5.7%), fundamental frequency is intermediate (5 to 13%) and durations vary most widely (18 to 60%). Boatwhistles, with the smallest variation and greatest amplitude, are likely generated by a maximal output of the CNS and sonic muscles. Grunt SPLs however, vary over a range of 26 dB for all fish and by as much as 18 dB in an individual, suggesting recruitment of variable numbers of motor units despite electrical coupling within the sonic motor nucleus.Abbreviations AC anterior commissure - CNS central nervous system - DHT dihydrotestosterone - Dm medial nucleus of dorsal telenecphalon - DTAM dorsal tegmental area of medulla - E estrogen - HRP horseradish peroxidase - PM nucleus praeopticus magnocellularis - POA preoptic area - PPa nucleus praeopticus parvocellularis anterior - SMA sonic motor area - SMN sonic motor nucleus - SPL sound pressure level - T testosterone - VS supracommissural nucleus of ventral telencephalon - Vv ventral nucleus of ventral telencephalon     

Development of the respiratory swimbladder of Pangasius sutchi

The swimbladder of Pangusius sutchi first appears on the dorsal surface of the oesophagus at about 5 days after hatching. The swimbladder has double chambers when it is separated by a medial septum at 8–10 days. Alveoli start to develop and function in air-breathing at 12–14 days. Their number is increased by subdivision, and the respiratory portion grows towards the centre. Morphometric analysis shows that the swimbladder increases in respiratory surface, volume and surface area: volume ratio during development. On a histological basis, the development of the swimbladder is divided into three distinct periods: a blind tube, a double chamber and an alveolus period. It is characteristic that the flat epithelial cell arises from a primordial cuboidal cell and that a double capillary system is arranged in the interalveolar septa. Multilamellar bodies appear and a blood-air barrier is established when the swimbladder becomes functional.