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PubMedDate not supplied

A case of an infertile man with short-tailed spermatozoa.

Ejaculated spermatozoa from an infertile patient were examined by scanning and transmission electron microscopy. All spermatozoa had abnormalities in the tail region. The abnormalities were divided into three types: (a) spermatozoa with a spherical tail. The tail was larger than the head in volume. This type of abnormality accounted for about 60% of the population; (b) spermatozoa with a blunt tail. The tails were about 2 microns in diameter and about 7 microns in length. This type of abnormality accounted for about 30% of the population of an ejaculate; (c) spermatozoa without a tail. Some of these had only a rudimentary tail. About 10% of the population belonged to this type. In types A and B, all components of the tail, except for dynein arms, were observed, but they were severely disarranged. Biopsy specimens of the testes and of the nasal mucosa of this patient were also investigated. The testicular biopsy showed defects in manchette formation. Normal development of the manchette could not be observed. The nasal epithelium showed absence of the inner dynein arms in the cilia.

Adult↗
PubMedDate not supplied

Physiology of heat loss from an extremity: the tail of the rat.

1. Hooded, conscious, male, laboratory rats were subjected to an ambient dry bulb temperature cycle between 12 degrees C and 35 degrees C over a period of approximately 5.5 h. The same procedure was followed using rats in which the temperature surrounding the tail was held constant, and using dead rats. 2. Temperature of the ambient air, and the rectum, flank skin, tail base and tail tip were measured during each ambient temperature cycle. 3. In both living and dead rats, a hysteresis loop was demonstrated for the relationship between all body temperatures measured and ambient temperature. 4. The hysteresis loops for tail temperature differed between living and dead rats in such a way as to indicate that tail temperature began to increase, as a result of an active process, at approximately 30 degrees C, but this response ceased at a lower temperature. 5. The results on rats in which tail ambient temperature was held constant agreed with the preceeding observations. 6. Clear evidence of a counter-current heat exchange system in the vasculature of the rat's tail was not obtained. 7. It is concluded that the tail of the rat resembles an on/off controller in its mode of operation.

Animals↗
PubMed1994

Magnitude, origin, and implications of the discrepancy between blood ethanol concentrations of tail vein and arterial blood of the rat.

The rat is widely used as an animal model for experiments involving ethanol, and alcohol concentrations in blood obtained from the tail routinely are used to monitor ethanol exposure and metabolism. The present study demonstrates that during periods of rising and declining ethanol levels, the alcohol concentrations in tail vein blood lags far behind that of arterial, jugular, or femoral vein blood. As a result, tail vein ethanol concentrations markedly underestimate the concentration in arterial blood and rapidly perfused tissue during periods of increasing body ethanol, whereas the reverse is true as body ethanol declines. This discrepancy, which appeared to result from the low blood perfusion:tissue water ratio in the tail, disappeared when the tail was heated to 37 degrees C. Compared with arterial blood, alcohol measurements performed on tail vein blood yielded a much higher apparent Km for ethanol clearance and a somewhat lower estimate of ethanol reaching the peripheral circulation. We conclude that, for a variety of studies, analyses of arterialized blood from the heated tail should yield a more accurate and reproducible measure of ethanol exposure and/or metabolism than does the conventional collection from the unheated tail.

Alcohol Drinking↗
PubMed1996

Cosmetic tail docking of dogs.

The anatomy of the canine tail and its relationship to the physiological functions of the tail are described and the effect of tail docking on these is discussed. Current knowledge on the physiology and anatomy of pain is described with particular reference to cosmetic tail docking in the neonatal puppy. Recent advances in knowledge about pain and the changes in approach to pain management, refute the premise that 'puppies do not feel pain therefore tail docking is not inhumane' and also the premise that 'the pain and the effects of tail docking are insignificant.' Six criteria to test the 'necessity' to dock dogs are presented; this article shows that the reasons advanced for tail docking do not satisfy these criteria and so that docking dogs' tails cannot be justified.

Amputation, Surgical↗
PubMed2002

Thermoregulatory control of sympathetic fibres supplying the rat's tail.

We investigated the thermoregulatory responses of sympathetic fibres supplying the tail in urethane-anaesthetised rats. When skin and rectal temperatures were kept above 39 degrees C, tail sympathetic fibre activity was low or absent. When the trunk skin was cooled episodically by 2-7 degrees C by a water jacket, tail sympathetic activity increased in a graded fashion below a threshold skin temperature of 37.8 +/- 0.6 degrees C, whether or not core (rectal) temperature changed. Repeated cooling episodes lowered body core temperature by 1.3-3.1 degrees C, and this independently activated tail sympathetic fibre activity, in a graded fashion, below a threshold rectal temperature of 38.4 +/- 0.2 degrees C. Tail blood flow showed corresponding graded vasoconstrictor responses to skin and core cooling, albeit over a limited range. Tail sympathetic activity was more sensitive to core than to trunk skin cooling by a factor that varied widely (24-fold) between animals. Combined skin and core cooling gave additive or facilitatory responses near threshold but occlusive interactions with stronger stimuli. Unilateral warming of the preoptic area reversibly inhibited tail sympathetic activity. This was true for activity generated by either skin or core cooling. Single tail sympathetic units behaved homogeneously. Their sensitivity to trunk skin cooling was 0.3 +/- 0.08 spikes s(-1) degrees C(-1) and to core cooling was 2.2 +/- 0.5 spikes s(-1) degrees C(-1). Their maximum sustained firing rate in the cold was 1.82 +/- 0.35 spikes s(-1).

Adrenergic Fibers↗
PubMed2002

Programmed translational frameshift in the bacteriophage P2 FETUD tail gene operon.

The major structural components of the P2 contractile tail are encoded in the FETUD tail gene operon. The sequences of genes F(I) and F(II), encoding the major tail sheath and tail tube proteins, have been reported previously (L. M. Temple, S. L. Forsburg, R. Calendar, and G. E. Christie, Virology 181:353-358, 1991). Sequence analysis of the remainder of this operon and the locations of amber mutations Eam30, Tam5, Tam64, Tam215, Uam25, Uam77, Uam92, and Dam6 and missense mutation Ets55 identified the coding regions for genes E, T, U, and D, completing the sequence determination of the P2 genome. Inspection of the DNA sequence revealed a new open reading frame overlapping the end of the essential tail gene E. Lack of an apparent translation initiation site and identification of a putative sequence for a programmed translational frameshift within the E gene suggested that this new reading frame (E') might be translated as an extension of gene E, following a -1 translational frameshift. Complementation analysis demonstrated that E' was essential for P2 lytic growth. Analysis of fusion polypeptides verified that this reading frame was translated as a -1 frameshift extension of gpE, with a frequency of approximately 10%. The arrangement of these two genes within the tail gene cluster of phage P2 and their coupling via a translational frameshift appears to be conserved among P2-related phages. This arrangement shows a striking parallel to the organization in the tail gene cluster of phage lambda, despite a lack of amino acid sequence similarity between the tail gene products of these phage families.

Amino Acid Sequence↗
PubMed2004

Comparison of simultaneous measurement of mouse systolic arterial blood pressure by radiotelemetry and tail-cuff methods.

Radiotelemetry of mouse blood pressure accurately monitors systolic pressure, diastolic pressure, heart rate, and locomotor activity but requires surgical implantation. Noninvasive measurements of indirect systolic blood pressure have long been available for larger rodents and now are being reported more frequently for mice. This study compared mouse systolic arterial blood pressure measurements using implanted radiotelemetry pressure transducer with simultaneous tail-cuff measurements in the same unanesthetized mice. The pressure range for comparison was extended by inducing experimental hypertension or by observations of circadian elevations between 3 AM and 6 AM. Both trained and untrained tail-cuff operators used both instruments. Every effort was made to follow recommended manufacturer's instructions. With the initial flow-based tail-cuff instrument, we made 671 comparisons (89 sessions) and found the slope of the linear regression to be 0.118, suggesting poor agreement. In an independent assessment, 277 comparisons (35 sessions) of radiotelemetry measurements with the pulse based tail-cuff instrument were made. The slope of the linear regression of the simultaneous measurements of systolic pressures was 0.98, suggesting agreement. Bland-Altman analysis also supported our interpretation of the linear regression. Thus although reliable systolic pressure measurements are possible with either tail-cuff or radiotelemetry techniques, in our hands some tail-cuff instruments fail to accurately detect elevated blood pressures. These data, however, do not distinguish whether this instrument-specific tail-cuff failure was due to operator or instrument inadequacies. We strongly advise investigators to obtain an independent and simultaneous validation of tail-cuff determinations of mouse blood pressure before making critical genotyping determinations.

Animals↗
PubMed1984

Hemodynamics and interstitial fluid pressure in the rat tail.

Blood flow in the rat was measured during pentobarbital anesthesia by plethysmographic and thermometric techniques. Tail arterial and venous pressures (Pa and Pv) were measured by glass micropipettes and interstitial fluid pressure (PIF) by wick-in-needle technique. Large pressure gradients were measured along the tail, Pa decreasing and Pv increasing toward the tip. In the vasoconstricted tail, distal arterial and venous pressures (Pad and Pvd, respectively, 10 cm from the tail root) were 55 and 11% of aortic pressure (PA), while PIF was 0-2 mmHg. Plasma volume expansion increased blood flow by a factor of 10 to 35. Pad rose to 74% and Pvd to 20% of PA. PIF increased to 15 mmHg, in parallel with Pv. Venous stasis (cuff pressure 14.7 mmHg) increased PIF and Pv by 3.5 and 9 mmHg, respectively, while tail volume increased by 0.4 to 1.2%. In conclusion, the large flow increase induced by plasma volume expansion depends strongly on dilation of the tail artery, with two- to threefold increase in internal radius. Simultaneously the tail veins relax and expand. Subcutaneous tissue is compressed between the expanding vessels and the tight skin, and PIF increases almost sufficiently to prevent a rise in net capillary filtration pressure. This immediate edema-preventing mechanism is less efficient during venous stasis, which presumably does not induce "active" dilation of the tail vessels. Similar mechanisms probably exist in other "encapsulated" tissues.

Animals↗
PubMed1995

Motor neuronal control of tail-directed and head-directed siphon responses in Aplysia californica.

1. Cutaneous stimulation of opposite ends of the body causes qualitatively different siphon responses: tail stimulation causes flaring and backward bending (the siphon T response), whereas head stimulation causes constriction and slight anterior bending (the siphon H response). This paper characterizes the motor neuronal control of siphon T and siphon H responses. 2. The siphon response to tail nerve (p9) shock in a semi-intact preparation was indistinguishable from the siphon T response in intact or parapodectomized animals. Similarly, the siphon response to head nerve (c2) shock in this preparation was indistinguishable from the siphon H response in intact or parapodectomized animals. 3. Central siphon motor neurons (SMNs) were found to cause a wider variety of movements than previously reported. The movements produced by the LFSB cells strongly resemble the flaring response of the siphon to tail or tail nerve stimulation. The movements produced by RDS and LDS1 resemble components of the constricting response of the siphon to head or head nerve stimulation. 4. Among central SMNs, the LFSB cells show the strongest activation by posterior stimulation, whereas RDS and LDS1 show the strongest activation by anterior stimulation. The LFSA cells, which produce much weaker siphon constriction, are only activated slightly by posterior stimulation and are inhibited by anterior stimulation. Peripheral SMNs are inhibited by stimulation of head and tail nerves, and thus their activity does not directly contribute to siphon T and H responses. 5. Artificially activating central SMNs with the pattern of activity previously exhibited after tail or head nerve stimulation indicated the sufficiency of the LFSB cells for the siphon T response, and of RDS and LDS1 for the siphon H response. 6. Dramatic behavioral deficits produced by hyperpolarizing the LFSB cells during tail nerve stimulation, or by hyperpolarizing RDS and LDS1 during head nerve stimulation, indicated the necessity of these cells for the expression of directed siphon responses to tail or head stimulation, respectively. 7. Because of their apparent necessity and sufficiency for directional siphon responses to anterior and posterior stimulation, these few cells provide well-defined vantage points for studying neural mechanisms underlying the motor control and transformation of siphon responses. The four LFSB cells offer a special advantage for cellular analysis because they form a homogeneous functional unit in which any sampled LFSB cell can be used as a precise monitor of the total motor output underlying the siphon T response.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1993

Three cases with different types of short-tailed spermatozoa.

Short-tailed spermatozoa were found in 3 men attending our subfertility clinic. Light microscopy revealed basically normal sperm heads, but a short tail was found in 90% or more of the spermatozoa. Scanning and transmission electron-microscopic examinations of the ejaculate revealed several types of short-tailed spermatozoa. In one case, the majority of the spermatozoa had a short, thick tail. In another case, all the spermatozoa were short-tailed, although two different types could be distinguished. As in the first case some spermatozoa were short- and thick-tailed, whereas others possessed an incomplete neck and middle piece, and a short, thick principal piece. In the third case, an elongated middle piece and short principal piece were found in almost all the short-tailed spermatozoa. Our electron-microscopic study revealed that the type of short-tailed spermatozoa was different in each patient.

Adult↗
PubMed2005

Acoustic characteristics of underwater tail slaps used by Norwegian and Icelandic killer whales (Orcinus orca) to debilitate herring (Clupea harengus).

Norwegian killer whales debilitate prey by slapping their tails into herring schools. These underwater tail slaps produce a thud-like sound. It is unclear whether this sound is caused by cavitation and/or physical contact between herring and whale tail. Also the forces causing debilitation of the fish are not understood. Here we present an acoustic analysis of underwater tail slaps using a multi-channel wide (150 kHz) band recording system. Underwater tail slaps produced by Norwegian killer whales generated sounds consisting of multiple pulses with source levels of 186+/-5.4 dB (pp) re.1 microPa at 1 m (+/-1 s.d., N = 4). The -3 dB and 97% energy bandwidths were 36.8+/-22.5 kHz and 130.5+/-17.5 kHz (+/-1 s.d., N = 13), respectively, with a centre frequency of 46.1+/-22.3 kHz. The similarities between the acoustic properties of underwater tail slaps recorded from killer whales in Norway, and thud-like sounds recorded from killer whales in Iceland suggest that Norwegian and Icelandic killer whales use similar hunting techniques. The acoustic characteristics of sounds produced by underwater tail slaps were similar to the ones from other cavitation sound sources described in the literature, both in term of temporal and frequency features as well as in source level. We suggest that multiple factors generated by the tail slaps like particle fluctuations, turbulence, pressure changes and physical impact cause debilitation of herring.

Acoustics↗
PubMed2001

[Assessment of anti-tremorogenic drugs using nicotine-induced tail-tremor model and elucidation of the mechanism].

Repeated administration of nicotine causes a tremor only in the tail (tail-tremor) of rats. The tremor is accompanied with locomotor hyperactivity without rigidity and immobility of the whole body, suggesting the involvement of the mechanism associated with the movement. The tail-tremor induced by nicotine was suppressed by nicotinic acethylcholine (nACh) receptor antagonists, but not by muscarinic acethylcholine (mACh) receptor antagonists. Moreover, the tail-tremor was suppressed by beta-adrenoceptor antagonists and benzodizepines. The tremor at rest is observed only in Parkinson's disease, which is improved by the use of mACh receptor antagonists. An essential tremor is one of the typical tremor connected with the movement (postural tremor) and improved with beta-adrenoceptor antagonists. These findings and results suggest that the nicotine-induced tail-tremor is useful for the study of the essential tremor as an animal model. On the other hand, daily administration of nicotine resulted in an augmentation of the tail-tremor. The development of the tail-tremor was suppressed by nACh receptor antagonists, N-methyl-D-aspartate (NMDA) receptor antagonists and nitric oxide (NO) synthase inhibitors. These results suggest that central nACh receptors are essential for the onset and further development of the tail-tremor induced by repeated administration of nicotine, and that NO formation mediated by NMDA receptors is involved in the developmental mechanisms.

Adrenergic beta-Antagonists↗
PubMed2006

A sex difference in the cortisol response to tail docking and ACTH develops between 1 and 8 weeks of age in lambs.

It is important to understand factors that may influence responses to stress, as these factors may also influence vulnerability to pathologies that can develop when stress responses are excessive or prolonged. It is clear that, in adults, the sex of an individual can influence the cortisol response to stress in a stressor specific manner. Nevertheless, the stage of development at which these sex differences emerge is unknown. We tested the hypothesis that there are sex differences in the cortisol response to tail docking and ACTH in lambs of 1 and 8 weeks of age. We also established cortisol responses in males when tail docking was imposed alone and in combination with castration at these ages. In experiment 1, 1 and 8 week old male and female lambs were subjected to sham handling, tail docking or, in males, a combination of tail docking and castration. In experiment 2, we administered ACTH (1.0 IU/kg) to male and female lambs at 1 and 8 weeks of age. There were significant cortisol responses to all treatments at both ages. Sex differences in the cortisol responses to tail docking and ACTH developed between 1 and 8 weeks of age, with females having greater responses than males. The data suggest that the mechanism for the sex difference in response to tail docking may involve the adrenal glands. At both ages, in males, the cortisol response to the combined treatment of tail docking and castration was significantly greater than that for tail docking alone.

Adrenal Glands↗
PubMedDate not supplied

Coccygeal muscle injury in English Pointers (limber tail).

A condition colloquially referred to as "limber tail" and "cold tail" is familiar to people working with hunting dogs, primarily Pointers and Labrador Retrievers. The typical case consists of an adult dog that suddenly develops a flaccid tail. The tail either hangs down from the tail base or is held out horizontally for several inches from the tail base and then hangs straight down or at some degree below horizontal. Initially, the hair on the dorsal aspect of the proximal tail may be raised and dogs may resent palpation of the area 3-4 inches (8-10 cm) from the tail base. Most dogs recover spontaneously within a few days to weeks. Anecdotal reports suggest that anti-inflammatory drugs administered within 24 hours after onset hasten recovery. Less than one half of affected dogs experience a recurrence. Affected Pointers almost always have a history of prolonged cage transport, a hard workout the previous day, or exposure to cold or wet weather Most owners and trainers familiar with the condition do not seek veterinary assistance. In cases where people are not familiar with this disease, other conditions such as a fracture, spinal cord disease, impacted anal glands, or prostatic disease have been incorrectly diagnosed. We examined 4 affected Pointers and found evidence of coccygeal muscle damage, which included mild elevation of creatine kinase early after onset of clinical signs, needle electromyographic examination showing abnormal spontaneous discharges restricted to the coccygeal muscles several days after onset, and histopathologic evidence of muscle fiber damage. Specific muscle groups, namely the laterally positioned intertransversarius ventralis caudalis muscles, were affected most severely. Abnormal findings on thermography and scintigraphy further supported the diagnosis.

Animals↗
PubMed2006

Long tails affect swimming performance and habitat choice in the male guppy.

Sexual selection often favors male secondary sexual traits, although in some cases the elaborate traits incur costs to the males with respect to natural selection. Males of the guppy Poecilia reticulata have longer tails (caudal fins) than females, and the long tails contribute to the mating success of the males through female mate choice. We examined the effect of tail length on the swimming performance of male and female guppies. In a laboratory experiment, males with longer tails exhibited poorer swimming performance than those with shorter tails. However, this effect was not apparent in females. In addition, in a feral population, tail length of males was negatively correlated with water flow velocity in their microhabitats. Although body size of females was negatively correlated with water flow velocity in their microhabitats, tail length of females showed no significant correlation with degree of water flow. These results suggest that the long tail of male guppies incurs costs, such as a decrease in swimming performance, to the males with respect to natural selection and consequently limits their choice of habitats to those with slow water flow.

Animals↗
PubMed1999

The musculature of the mouse tail is characterized by metameric arrangements of bicipital muscles.

This is the first report, to our knowledge, of the full characterization of the musculature of the mouse tail. Bicipital muscles form a major part of the tail musculature. The tail tendons originate with fusiform muscle from the dorsal and ventral lumbo-sacro-coxal regions and are inserted into the coccygeal vertebrae (extrinsic muscles of the tail). Each coccygeal vertebra has short muscles that terminate on the adjacent vertebrae (intrinsic muscles of the tail). The short muscle and its corresponding tail tendon are joined, thereby forming a bicipital muscle that is inserted into the coccygeal process. A geographical correspondence is strictly maintained between the origin of the tendon in the lumbo-sacro-coxal region and the insertion of the bicipital muscle in the coccygeal vertebrae. In other words, the organization of the tail musculature is based upon repetitions of fusion between the extrinsic and intrinsic muscles at each coccygeal vertebral level. This design is referred to as the metameric arrangement of the bicipital muscles. The organization, arrangement and function of muscles in the tail have features in common with those muscles in the digits of the human extremities.

Anatomy, Artistic↗
PubMed1983

The effects of changes in the environmental temperature on the growth of tail bones in the mouse.

The tails of baby mice grow rapidly and independently of environmental temperature because they are kept warm by their mothers. After weaning, at approximately 3 weeks of age, tail growth is strictly related to environmental temperatures. During the first 2 weeks after weaning growth rates of 1.2-1.4 mm/day/tail were seen at 33 degrees and a maximum of 2.43 mm/day/tail was observed in one group kept at 36 degrees. Animals kept at 8 degrees or 4 degrees showed tail growth rates of 0.4 mm/day or less. However, the tails of animals transferred from either hot to cold or cold to hot during their first 2 weeks after weaning immediately grew at the same rate as those of animals kept in these conditions continuously, thus indicating that heat was acting directly on bone growth. The tails of animals kept continuously in the hot environment at 33 degrees completed their growth early so that their growth rate fell below that of controls after about 3 weeks of treatment (when they were 6-7 weeks old) and below that of "cold" animals after about 4 weeks (7-8 weeks old). The tails of the "control" and "cold" animals grew slowly for a very long time, 150-195 days. Even so, because of the very rapid early growth of tails in the hot environment, their final length was always greater than either the "control" or "cold" tails.

Aging↗
PubMed1997

Isolation of cDNA clones for genes that are expressed in the tail region of the ascidian tailbud embryo.

An ascidian tailbud embryo is comprised of the anterior trunk and posterior tail. We constructed cDNA libraries of the tail region and trunk region of the ascidian Halocynthia roretzi. The screening of the tail library by tail single-stranded cDNA minus the trunk library RNA as a probe, yielded cDNA clones for genes that are expressed in the tail epidermis, visceral ganglion, trunk lateral cells, muscle cells, and certain regions of the tail. Among them, a cDNA clone for a gene designated HrPost-1 is described in detail. HrPost-1 encodes a novel, possible secreted protein of 238 amino acids. The expression of the gene is zygotic. HrPost-1 transcript was first evident in the posterior B-line blastomeres including muscle cells and endodermal strand cells of the gastrula-stage embryo, and the expression in these regions disappeared by the early tailbud stage. Around neurulation, the HrPost-1 transcript appeared in epidermal cells of the posterior-most region of the embryo. As development proceeded, the gene expression spread anteriorly in the epidermal cells of the neurula and tailbud embryo, and thus at the early-to-mid tailbud stage, HrPost-1 expression appeared to define the boundary between the trunk and tail epidermis. These results suggest that, in addition to tissue-specific genes, the activities of a set of region-specific genes are associated with tail formation in the ascidian embryo.

Amino Acid Sequence↗