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  • 1
    Online Resource
    Online Resource
    Sharjah :Bentham Science Publishers,
    Keywords: Spermatozoa. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (457 pages)
    Edition: 1st ed.
    ISBN: 9781681081281
    Language: English
    Note: Intro -- CONTENTS -- FOREWORD -- ACKNOWLEDGEMENTS -- DEDICATION -- List of Contributors -- ABOUT THE AUTHORS -- The Flagellar Mechanics of Spermatozoa and its Regulation -- INTRODUCTION -- 1. STRUCTURE, BIOCHEMICAL COMPOSITION AND BUILDING OF AN AXONEME -- 1-1. Structure -- 1-2. Biochemical Composition -- 1-3. The Structural and Biochemical Complexity of the Flagellar Axoneme -- 1-4. The Building of an Axoneme -- 2. BIOPHYSICAL PARAMETERS OF BEATING FLAGELLA THAT GOVERN SPERM MOTILITY -- 3. OPERATION OF A FLAGELLAR MICROMOTOR -- 3-1. Cilia and Flagella Use Similar Elements for Their Functioning -- 3-2. Notion of Sliding -- 3-3. Bending Engendered by the Sliding -- 3-4. Regulation Responsible of Alternative Movement -- 3-5. Enzymological and Structural Data on the Flagellar Micro-Motor -- 3-6. Need for a Resistance to Sliding -- 4. OPERATIONAL MODELS -- 4-1. Presentation of the Main Models -- 4-2. Wave Propagation -- 4-2-1. Curvature-controlled Model -- 4-2-2. Sliding-controlled Switching Model -- 4-3. Predictions on the Mechanism for Regulation of Waves and Its Consequences -- 5. INTERNAL VERSUS EXTERNAL REGULATION OF AXONEMAL ACTIVITY -- 5-1. Internal Regulation -- 5-2. Regulatory Complexes in the Axoneme -- 5-3. External Regulation -- 5-4. Initiation of Flagella Activity: Biochemical Aspects -- 5-5. Mechanisms Underlying Motility Maturation and Activation Events -- 5-6. Initiation of Flagella Activity: Phenomenological Aspects -- 6. ENERGETIC ASPECTS -- 6-1. Source and use of Energy: Biochemical Aspects -- 6-2. Force, Power and Energy in the Flagellum: Mechanical Aspects -- 7. EVOLUTIONARY CONSIDERATIONS ON THE AXONEMAL ORGANELLE AND ON THE SPERM GUIDANCE MECHANISMS -- 8. CONCLUSIONS ABOUT SPERM MOTILITY AND ITS ACTIVATION -- CONFLICT OF INTEREST -- ACKNOWLEDGEMENTS -- NOTIFICATION -- REFERENCES -- Sea Urchin Sperm Chemotaxis -- 1. INTRODUCTION. , 2. GAMETE COMMUNICATION, SENSING OF SPATIAL CUES -- 2.1. Sperm-Activating Peptides and the Taxonomy of Echinoids -- 2.2. SAP Receptors and the Membrane-Associated Guanylate Cyclase -- 2.3. Gradient Detection Constraints -- 3. SIGNALING -- 4. CA2+ SIGNALS AND FLAGELLAR DYNAMICS -- 5. CURRENT EFFORTS OF MODELING TO UNDERSTAND CHEMOTAXIS -- 5.1. Modeling Focused on Signaling -- 5.2. Modelling Focused on Sperm Chemotactic Movement -- 5.3. Efforts for Comprehensive Modelling -- PERSPECTIVES -- CONFLICT OF INTEREST -- ACKNOWLEDGEMENTS -- REFERENCES -- Sperm Chemotaxis in Urochordates -- INTRODUCTION -- FEATURES OF ASCIDIAN SPERM CHEMOTAXIS -- SPECIFICITY OF ASCIDIAN SPERM CHEMOTAXIS -- SIGNALING OF SPERM CHEMOTAXIS -- Sperm Attractants -- Receptor of Sperm Attractants -- Species Specificity of Sperm Chemotaxis Revisited: Discussion on the Molecular Basis of Specificity -- Sperm Attractants Induce Ca2+ Bursts in the Spermatozoa -- CONTROL OF SPERM FLAGELLAR MOVEMENT DURING CHEMOTAXIS -- [Ca2+]i Controls Sperm Flagellar Movement -- Molecular Components of the Axonemes in Ascidian Sperm -- Calaxin is a Ca2+-sensor Protein of Outer Arm Dynein -- Calaxin Drives Sperm Chemotaxis by Propagating Flagellar Asymmetric Waveform -- CONCLUSIONS -- CONFLICT OF INTEREST -- ACKNOWLEDGEMENTS -- REFERENCES -- Sperm Motility Initiation in Pacific Herring -- INTRODUCTION -- Herring Sperm Motility: Molecules that Initiate Motility -- Herring Sperm Motility: Extracellular Ion Requirements -- Initiation of Motility in Pacific Herring Sperm in the Estuary -- Signal Transduction Events Associated with Sperm Activation -- Motility Changes and Facilitation of Micropyle Entry via Increases in [Ca2+]i -- CONFLICT OF INTEREST -- ACKNOWLEDGEMENTS -- REFERENCES -- Sperm Guidance in Other Animals and Phylla (Such as Other Fish, Jelly-Fish, or Amphibian) -- INTRODUCTION. , 1. IN JELLY FISH: HYDROMEDUSAE AND SIPHONOPHORES -- In Hydromedusae -- In Another Example, Siphonophores -- 2. ECHINODERMS -- 3. IN FISHES -- 4. IN CORALS -- 5. IN AMPHIBIANS -- 6. IN HYDROIDS -- 7. IN UROCHORDATES -- 8. IN INSECTS -- 9. IN NEMATODES -- 10. IN MOLLUSKS -- 11. IN SQUIDS -- 12. ADDITIONAL SPERM GUIDANCE DEVICES -- 13. PHYSICOTAXIS -- 14. AN INTERMEDIATE SITUATION WHERE EXTERNAL GUIDANCE AND INTERNAL FERTILIZATION PROCESSES ARE COMBINED -- 15. SITUATION OF SPERMATOZOA IN THE PLANTS PHYLLUM -- 16. OTHER EXAMPLES OF CELL GUIDANCE: PHOTOTAXIS, GEOTAXIS -- 17. THE ACROSOMAL FILAMENT: AN ANCHORING DEVICE USED IN SOME SPECIES AS A CLEVER GUIDANCE SYSTEM FOR THE SPERMATOZOON -- 18. THE ULTIMATE MEETING STEP: MALE PRONUCLEUS GUIDED BY FEMALE PRIOR TO UNION IN THE ZYGOTE -- 19. CONCLUSIONS -- NOTIFICATION -- CONFLICT OF INTEREST -- ACKNOWLEDGEMENTS -- REFERENCES -- Mammalian Sperm Guidance - An Overview -- CONFLICT OF INTEREST -- ACKNOWLEDGEMENTS -- REFERENCES -- Sperm Chemotaxis in Mammals -- INTRODUCTION -- FEATURES OF MAMMAL SPERM CHEMOTAXIS -- METHODS OF STUDYING SPERM CHEMOTAXIS IN MAMMALS -- Methods of Studying Sperm Chemotaxis -- Sperm Accumulation Assay -- Sperm Directionality Assay -- Microfluidic Assay -- Experimental Conditions -- CHEMOATTRACTANTS AND THEIR PRESUMPTIVE BIOLOGICAL SOURCES -- Biological Sources of Attractants -- Follicular Fluid -- Oviductal Fluid -- Cumulus-oocyte Complex -- Chemoattractants -- N- formyl Methyl Peptides -- Atrial Natriuretic Peptide (ANP) -- Chemokines -- Progesterone -- Nitric Oxide -- Odorants -- Cyclic Nucleotides -- Allurin -- Attractants of Unknown Identity -- MOLECULAR MECHANISM OF SPERM CHEMOTAXIS -- BIOLOGICAL FUNCTION OF SPERM CHEMOTAXIS -- CONCLUDING REMARKS -- CONFLICT OF INTEREST -- ACKNOWLEDGEMENTS -- ABBREVIATIONS -- REFERENCES -- Mammalian Sperm Behavior During Thermotaxis. , INTRODUCTION -- KINETIC RESPONSE OF HUMAN SPERMATOZOA TO A TEMPER-ATURE SHIFT -- FLAGELLAR RESPONSE AND DIRECTIONAL CHANGES IN SPERM SWIMMING -- HYPERACTIVATION IN HUMAN SPERM -- TEMPERATURE SENSING IN THERMOTAXIS -- A MODEL OF SPERM BEHAVIOR IN A SPATIAL TEMPERATURE GRADIENT DURING THERMOTAXIS -- CONFLICT OF INTEREST -- ACKNOWLEDGEMENTS -- REFERENCES -- Modelling Spermatozoan Swimming: Its Capabilities and Limitations for Contributing to the Understanding of Sperm Guidance -- 1. INTRODUCTION -- 2. AN OVERVIEW OF SPERM MODELLING -- 2.1. The Fundamental Mechanics of Swimming -- 2.1.1. Navier-Stokes Equations. A Qualitative Summary -- 2.1.2. The Mechanical Mechanism of Sperm Swimming -- 2.1.3. Quantitative Analysis -- 2.2. Further Theories -- 2.2.1. Multiscale Models, Featuring Intra-flagellar Dynamics -- 3. GUIDANCE CUES -- 3.1. Chemotaxis -- 3.2. Thigmotaxis -- 3.3. Rheotaxis -- 3.4. Thermotaxis -- 3.5. Other Guidance Cues -- 3.5.1. Viscotaxis -- 3.5.2. Advection in Fast Flow -- 4. LINKING INDIVIDUAL GUIDANCE TO POPULATION SCALE BEHAVIOUR -- CONCLUDING REMARKS -- CONFLICT OF INTEREST -- ACKNOWLEDGEMENTS -- REFERENCES -- Sperm Guidance: Comparison with Motility Regulation in Bikont Species -- INTRODUCTION -- 1. FLAGELLAR REGULATION IN SPERM CHEMOTAXIS -- 1-1. Pattern of Flagellar Movement in Chemotaxis -- 1-2. Molecular Mechanisms of Transient Change in Sperm Flagellar Waveform -- 2- FLAGELLAR MOVEMENTS: ANIMAL SPERM VS. BIKONT SPECIES -- 3. PHOTO-RESPONSE IN THE GREEN ALGA CHLAMYDOMONAS (ARCHAEPLASTIDA) -- 3-1. Phototaxis in Chlamydomonas -- 3-2. Flagellar Movements During Phototaxis in Chlamydomonas -- 3-3. Conversion of Flagellar Symmetry/Asymmetry by Ca2+ in Photophobic Response -- 4. UNEQUAL REGULATION OF TWO FLAGELLA IN BROWN ALGAE (STRAMENOPILES) -- 5. REGULATION OF TWO DISTINCT FLAGELLA IN DINOFLAGELLATES (ALVEOLATA). , 6. FLAGELLAR MOTILITY IN OTHER ALGAL SPECIES -- 6-1. Prasinophytes -- 6-2. Haptophytes -- 6-3. Diatoms -- 7. CILIARY RESPONSE AND CA2+ REGULATION IN CILIATES (ALVEOLATA) -- 7-1. Paramecium -- 7-2. Tetrahymena -- 8. MODULATION OF FLAGELLAR MOVEMENT IN TRYPANOSOMA AND EUGLENA (EXCAVATA) -- 8-1. Trypanosoma -- 8-2. Euglena -- 9. OVERALL CONSIDERATIONS: EVOLUTIONARY POINT OF VIEW ON CILIARY AND FLAGELLAR MOTILITY -- CONFLICT OF INTEREST -- ACKNOWLEDGEMENTS -- REFERENCES -- Sperm Guidance: Chemotactic Features Common to Sperm in Various Species -- INTRODUCTION -- 1. THE KEY ROLES OF CA2+ IONS, CAMP AND PROTEIN PHOSPHORYLATION -- 2. RELATIONSHIP BETWEEN "SPERM GUIDANCE" DEFINITIONS AND METHODOLOGIES EMPLOYED TO DEMONSTRATE IT -- 3. TENTATIVE DISTINCTION BETWEEN ACTIVATION AND ATTRACTION MECHANISMS -- 4. MAIN LAWS GOVERNING SPERM CHEMOTAXIS? -- 5. EFFICIENCY OF CHEMOTAXIS -- 6. WHY ADDITIONAL SPERM GUIDANCE DEVICES? -- NOTIFICATION -- CONFLICT OF INTEREST -- ACKNOWLEDGEMENTS -- REFERENCES -- Conclusions on Sperm Guidance Features -- REFERENCES -- Appendix -- SUBJECT INDEX.
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  • 2
    ISSN: 1365-2109
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Determination of semen quality is necessary to understand the basic biochemical processes occurring during motility of sperm and during fertilization to evaluate the reproductive ability of different fish species and to create an optimal environment for storage of spermatozoa; in this regard less information is available for Acipenseridae compared with Cyprinidae and Salmonidae. The aim of the present study is to determine chemical composition and osmolality of seminal fluid and their relationship with sperm motility in Acipenser persicus. The results obtained show that sodium (Na+), chloride (Cl−) and potassium (K+) were predominant ions in the seminal plasma and the average of osmolality of seminal plasma was 82.56 mOsm kg−1. The higher chemical contents and osmolality compared with other sturgeon species reveal species-specific characteristics and high secretory activity of spermatic duct in A. persicus. Significant positive correlations were observed between osmolality-Cl−, Na+-osmolality and Na+–Cl− (P〈0.05, P〈0.001 and P〈0.05 respectively). But statistically significant correlation was not observed between seminal plasma parameters and sperm motility. Probably, the Na+ and Cl− are the main electrolytes playing a major role in maintaining the osmolality of the seminal plasma and the viability of the spermatozoa in vivo.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Aquaculture research 36 (2005), S. 0 
    ISSN: 1365-2109
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: The motility and fertilizing ability of the Persian sturgeon, Acipenser persicus, spermatozoa were investigated. Optimum ionic content (Na+, K+, Ca2+ and Mg2+) and pH of activation solution as well as the optimum dilution rate were determined. The results show optimum motility characteristics of spermatozoa in buffered solutions containing 25, 0.2, 3 and 10 mM L−1 Na+, K+, Ca2+ and Mg2+, respectively, at dilution rate 1:50 and pH 8.0. To test the fertilizing ability of sperm, two buffered saline solutions were used as activation solution of sperm motility. The present study indicated (1) spermatozoa motility is one of key factors that influence on fertilizing ability of sperm, (2) a high fertilizing ability of sperm is obtained after dilution in saline solutions rather than in freshwater and (3) a maximum fertilization rate occurs in buffered saline solution containing 0.2 mM L−1 K+. There is also a good correlation between biochemical characteristics of seminal plasma and fertilizing ability of sperm.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-5133
    Keywords: Sperm biology ; Sperm movement ; Sperm diluent ; Marine fish
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Synopsis Turbot sperm motility is observed using dark field microscopy and stroboscopic illumination combined with video recording. Sperm motility is triggered by dilution of spermatozoa in sea water or in non ionic media (glucose or saccharose), presenting osmotic pressure ranging from 300 to 2100 mOsmol. The percentage of motile spermatozoa reaches 100% under conditions of osmotic pressure of 300 to 1100 mOsmol and pH close to 8.0. In full sea water, glucose or saccharose solutions an agglutination of spermatozoa is observed; this is prevented by addition of bovine serum albumin (5 mg ml−1). Immediately after transfer in activation solutions, 100% spermatozoa are motile in most samples freshly stripped. This percentage drops suddenly between 15 and 30% after 70 to 100 sec. The beat frequency remains at a constant value of 50 Hz during 40 s post activation and then drops suddenly between 15 and 30 Hz. The spermatozoa velocity is about 200 micrometers s−1 during 30 to 40 s and then declines to a stable value of 100 micrometers s−1 at 50 s post activation. After 1.20 mn, more and more spermatozoa become motionless. The minimum calculated and averaged distance covered during 1.20 min, is about 12 mm. The high performances of turbot spermatozoa motility are interpreted as a compensatory mechanism for the low sperm production.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 6 (1986), S. 225-228 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 20 (1991), S. 55-68 
    ISSN: 0886-1544
    Keywords: motility ; spermatozoa ; calcium ; potassium ; pH ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The movement of live trout spermatozoa is very brief (25 sec at 20°C) and conditions have been developed to get synchronous initiation of sperm motility which allowed quantification of the major parameters of sperm movement during the motility phase.Recorded flagellar beat frequencies decreased steadily from values of 55 Hz at the beginning to 20 Hz at the end of the motility phase. Sperm forward velocities followed a similar pattern from 250 to 20 μm.sec-1 in the same conditions and the diameters of sperm trajectories were reduced from 370 to 40 μm. Thus none of the characteristics of sperm movement was constant during the motile phase which ended abruptly by a straightening of the flagella.The decrease in flagellar beat frequencies and sperm velocities are much greater than what could be extrapolated from the decrease of intracellular ATP (Christen R. et al: Eur. J. Biochem, 166:667-671, 1987) or from measurements of ATP-dependence of reactivated sperm velocities (Okuno M. and Morisawa N.: In Biological Functions of Microtubules and Related Structures. New York: Academic Press, pp. 151-162, 1982). Therefore, the cessation of flagellar beating at 25 sec is not directly the result of the low concentration of intracellular ATP.The decrease in the diameters of sperm trajectories which occurred during the first part of the motility phase was correlated with [Ca]i measurements (Cosson M.P. et al, Cell Motil. Cytoskeleton, 14:424-434, 1989). The effect of Ca2+ at the axonemal level does not indicates that Ca2+ influx is previous to flagellar beating but rather suggests a classical Ca2+ regulation of the flagellar assymetry.The short duration of the motility phase and the characteristics of sperm movement were very similar in various conditions (high external K+, low pH media) where increased external Ca2+ or divalent ions were shown to overcome K+ and H+ inhibition of sperm motility, both conditions which have been shown to depolarize the plasma membrane potential (Gatti J.L. et al: J. Cell Physiol., 143:546-554, 1990).The present study of the parameters of sperm movement suggests that once motility is initiated, a defined set of axonemal events will take place whatever the external conditions.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0886-1544
    Keywords: trout ; spermatozoa ; ATP ; cAMP ; axoneme ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Live trout spermatozoa initiate flagellar motility for only a short period (30 sec at 18°C) during which their mean beat frequency decreases steadily from 60 to 20 Hz. Motility then stops abruptly. Investigations of the activation of movement in demembranated sperm points to cyclic-AMP being necessary for reactivation (half effect at 0.5μm) in some conditions. cAMP acts mainly by increasing the percentage of motile cells and not the beat frequency (BF) of the flagellar axoneme. Dibutyryl cAMP does not initiate movement or prolong motility of live sperm.The initiation of movement of demembranted trout sperm was investigated in various incubation conditions relative to previous phases of in vivo movement and to ATP concentration. In the absence of cAMP and in the presence of ATP lower than 25 μM, all sperm celi models were active with BF up to 15-20 Hz whatever their previous physiological condition. In contrast, at ATP concentrations above 100 μM, the fraction of active spermatozoa decreased proportionally but the BF of the active ones increased so that, at 1 mM ATP up to 20 μM restored activity to 100% sperm models with a similar BF of 65 Hz.At ATP concentrations higher than 25 μM, cAMP was necessary in a concentration dependent manner in the reactivation, but not in the demembranation meduim. This dependence was found to be unrelated to a previous in vivo phase of movement. The antagonistic effects of ATP vs. cAMP were tested at various concentrations of both nucleotides: the apparent affinity for cAMP, measured as the concentration restoring movement of 50% cell models, was decreased from 15 nM at 0.1 mM ATP to 0.5 μM at 1 mM ATP; conversely, the affinity for ATP, measured as the concentration giving rise to the half maximal beat frequency, was not significautly affected when the concentration of cAMP was raised to 0.5 mM. Preincubation with phosphodiesterase (PDE) resulted in motility of 100% of sperm models even at low ATP concentration. This tends to show that cAMP must be constantly present to sustain motility.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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