Investigation of epididymal sperm maturation in the golden hamster

Summary During passage of hamster spermatozoa through the epididymis their maturation is shown to involve changes in the sperm head, midpiece (mitochondria) and tail. The sum of these changes results in a dramatic increase in the fertilizing potential of the spermatozoa. When comparable numbers of s...

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Veröffentlicht in:International journal of andrology 1994-10, Vol.17 (5), p.256-261
Hauptverfasser: WEISSENBERG, R., YOSSEFI, S., OSCHRY, Y., MADGAR, I., LEWIN, L. M.
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container_issue 5
container_start_page 256
container_title International journal of andrology
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creator WEISSENBERG, R.
YOSSEFI, S.
OSCHRY, Y.
MADGAR, I.
LEWIN, L. M.
description Summary During passage of hamster spermatozoa through the epididymis their maturation is shown to involve changes in the sperm head, midpiece (mitochondria) and tail. The sum of these changes results in a dramatic increase in the fertilizing potential of the spermatozoa. When comparable numbers of spermatozoa from the caput or corpus epididymis were injected into one uterine horn of mature females, following ovulation induction, and spermatozoa from the cauda epididymis were injected into the contralateral horn, no fertilization was observed with caput epididymal spermatozoa, 1.7% of oocytes were fertilized by corpus epiddymal spermatozoa, whereas 79.5% fertilization was obtained with cauda epididymal spermatozoa. Total sperm numbers increased from caput to corpus to cauda [28.3 ± 12.2, 40.6 ±20.8, 1434 ±62 mihon, respectively]. The percentage of progressively motile spermatozoa increased from 27.9 ±6.4 to 33.8 ± 4.8 to 70 ± 10.7 during this passage. Viability, measured by exclusion of the dye, propidium iodide, was significantly less in spermatozoa from the cauda than from the proximal or mid‐caput epididymis. The percentage of the live cells that were stained intensely by rhodamine‐123 (a measure of mitochondrial membrane potential) increased during epididymal passage from 22.8 ±7.8% in the proximal caput epididymis to 57.2 ± 16.5% in the cauda epididymis. Staining with acridine orange (a measure of DNA packaging in the sperm head) indicated an increase in chromatin condensation in cauda epididymal spermatozoa, when compared to those obtained from the caput or corpus.
doi_str_mv 10.1111/j.1365-2605.1994.tb01251.x
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The percentage of progressively motile spermatozoa increased from 27.9 ±6.4 to 33.8 ± 4.8 to 70 ± 10.7 during this passage. Viability, measured by exclusion of the dye, propidium iodide, was significantly less in spermatozoa from the cauda than from the proximal or mid‐caput epididymis. The percentage of the live cells that were stained intensely by rhodamine‐123 (a measure of mitochondrial membrane potential) increased during epididymal passage from 22.8 ±7.8% in the proximal caput epididymis to 57.2 ± 16.5% in the cauda epididymis. 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Psychology ; Intracellular Membranes - metabolism ; Male ; Mammalian male genital system ; Mesocricetus ; Microscopy, Fluorescence ; Mitochondria - metabolism ; mitochondrial function ; morphology ; Morphology. 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M.</creatorcontrib><title>Investigation of epididymal sperm maturation in the golden hamster</title><title>International journal of andrology</title><addtitle>Int J Androl</addtitle><description>Summary During passage of hamster spermatozoa through the epididymis their maturation is shown to involve changes in the sperm head, midpiece (mitochondria) and tail. The sum of these changes results in a dramatic increase in the fertilizing potential of the spermatozoa. When comparable numbers of spermatozoa from the caput or corpus epididymis were injected into one uterine horn of mature females, following ovulation induction, and spermatozoa from the cauda epididymis were injected into the contralateral horn, no fertilization was observed with caput epididymal spermatozoa, 1.7% of oocytes were fertilized by corpus epiddymal spermatozoa, whereas 79.5% fertilization was obtained with cauda epididymal spermatozoa. Total sperm numbers increased from caput to corpus to cauda [28.3 ± 12.2, 40.6 ±20.8, 1434 ±62 mihon, respectively]. The percentage of progressively motile spermatozoa increased from 27.9 ±6.4 to 33.8 ± 4.8 to 70 ± 10.7 during this passage. Viability, measured by exclusion of the dye, propidium iodide, was significantly less in spermatozoa from the cauda than from the proximal or mid‐caput epididymis. The percentage of the live cells that were stained intensely by rhodamine‐123 (a measure of mitochondrial membrane potential) increased during epididymal passage from 22.8 ±7.8% in the proximal caput epididymis to 57.2 ± 16.5% in the cauda epididymis. Staining with acridine orange (a measure of DNA packaging in the sperm head) indicated an increase in chromatin condensation in cauda epididymal spermatozoa, when compared to those obtained from the caput or corpus.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Chromatin - metabolism</subject><subject>chromatin condensation</subject><subject>Cricetinae</subject><subject>DNA packaging</subject><subject>epididymis</subject><subject>Epididymis - cytology</subject><subject>Female</subject><subject>fertilization</subject><subject>flow cytometry</subject><subject>Fluorescent Dyes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Intracellular Membranes - metabolism</subject><subject>Male</subject><subject>Mammalian male genital system</subject><subject>Mesocricetus</subject><subject>Microscopy, Fluorescence</subject><subject>Mitochondria - metabolism</subject><subject>mitochondrial function</subject><subject>morphology</subject><subject>Morphology. Physiology</subject><subject>motility</subject><subject>Rhodamine 123</subject><subject>Rhodamines</subject><subject>Sperm Maturation</subject><subject>spermatozoa</subject><subject>Spermatozoa - metabolism</subject><subject>Vertebrates: reproduction</subject><issn>0105-6263</issn><issn>1365-2605</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkEtv1DAUhS0EKkPhJyBFCLFL8NsOG1QqaAdGZQNiaTn2Teshj6mdgZl_j0eJZs_dWFfn3OOjD6E3BFckz_ttRZgUJZVYVKSueTU1mFBBqsMTtDpLT9EKEyxKSSV7jl6ktMUYM83IBbpQstZakBX6tB7-QJrCvZ3COBRjW8Au-OCPve2KtIPYF72d9nGWw1BMD1Dcj52HoXiwfZogvkTPWtsleLW8l-jnl88_rm_Lzfeb9fXVpnRc17IE61zbeNpoCgy88px5aT3wvDpb01YAtsJrRwlXoFVLFOdENZSDBQU1u0Tv5txdHB_3ubTpQ3LQdXaAcZ-MUhrrWvNs_DAbXRxTitCaXQy9jUdDsDkBNFtzomROlMwJoFkAmkM-fr38sm968OfThVjW3y66Tc52bbSDC-lsYwznFjTbPs62v6GD438UMOuvV3dUyJxQzgkhQz6cE2z8baRiSphfdzeGb6T-hiU2t-wfDCidYg</recordid><startdate>199410</startdate><enddate>199410</enddate><creator>WEISSENBERG, R.</creator><creator>YOSSEFI, S.</creator><creator>OSCHRY, Y.</creator><creator>MADGAR, I.</creator><creator>LEWIN, L. M.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199410</creationdate><title>Investigation of epididymal sperm maturation in the golden hamster</title><author>WEISSENBERG, R. ; YOSSEFI, S. ; OSCHRY, Y. ; MADGAR, I. ; LEWIN, L. M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4896-eaccfbd2b82e3ed7d43d6ade42e3ca92f5e0a5d8c2147e87f174417b24eae7e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Chromatin - metabolism</topic><topic>chromatin condensation</topic><topic>Cricetinae</topic><topic>DNA packaging</topic><topic>epididymis</topic><topic>Epididymis - cytology</topic><topic>Female</topic><topic>fertilization</topic><topic>flow cytometry</topic><topic>Fluorescent Dyes</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Intracellular Membranes - metabolism</topic><topic>Male</topic><topic>Mammalian male genital system</topic><topic>Mesocricetus</topic><topic>Microscopy, Fluorescence</topic><topic>Mitochondria - metabolism</topic><topic>mitochondrial function</topic><topic>morphology</topic><topic>Morphology. Physiology</topic><topic>motility</topic><topic>Rhodamine 123</topic><topic>Rhodamines</topic><topic>Sperm Maturation</topic><topic>spermatozoa</topic><topic>Spermatozoa - metabolism</topic><topic>Vertebrates: reproduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WEISSENBERG, R.</creatorcontrib><creatorcontrib>YOSSEFI, S.</creatorcontrib><creatorcontrib>OSCHRY, Y.</creatorcontrib><creatorcontrib>MADGAR, I.</creatorcontrib><creatorcontrib>LEWIN, L. 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M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigation of epididymal sperm maturation in the golden hamster</atitle><jtitle>International journal of andrology</jtitle><addtitle>Int J Androl</addtitle><date>1994-10</date><risdate>1994</risdate><volume>17</volume><issue>5</issue><spage>256</spage><epage>261</epage><pages>256-261</pages><issn>0105-6263</issn><eissn>1365-2605</eissn><coden>IJANDP</coden><abstract>Summary During passage of hamster spermatozoa through the epididymis their maturation is shown to involve changes in the sperm head, midpiece (mitochondria) and tail. The sum of these changes results in a dramatic increase in the fertilizing potential of the spermatozoa. When comparable numbers of spermatozoa from the caput or corpus epididymis were injected into one uterine horn of mature females, following ovulation induction, and spermatozoa from the cauda epididymis were injected into the contralateral horn, no fertilization was observed with caput epididymal spermatozoa, 1.7% of oocytes were fertilized by corpus epiddymal spermatozoa, whereas 79.5% fertilization was obtained with cauda epididymal spermatozoa. Total sperm numbers increased from caput to corpus to cauda [28.3 ± 12.2, 40.6 ±20.8, 1434 ±62 mihon, respectively]. The percentage of progressively motile spermatozoa increased from 27.9 ±6.4 to 33.8 ± 4.8 to 70 ± 10.7 during this passage. Viability, measured by exclusion of the dye, propidium iodide, was significantly less in spermatozoa from the cauda than from the proximal or mid‐caput epididymis. The percentage of the live cells that were stained intensely by rhodamine‐123 (a measure of mitochondrial membrane potential) increased during epididymal passage from 22.8 ±7.8% in the proximal caput epididymis to 57.2 ± 16.5% in the cauda epididymis. Staining with acridine orange (a measure of DNA packaging in the sperm head) indicated an increase in chromatin condensation in cauda epididymal spermatozoa, when compared to those obtained from the caput or corpus.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>7698851</pmid><doi>10.1111/j.1365-2605.1994.tb01251.x</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Biological and medical sciences
Chromatin - metabolism
chromatin condensation
Cricetinae
DNA packaging
epididymis
Epididymis - cytology
Female
fertilization
flow cytometry
Fluorescent Dyes
Fundamental and applied biological sciences. Psychology
Intracellular Membranes - metabolism
Male
Mammalian male genital system
Mesocricetus
Microscopy, Fluorescence
Mitochondria - metabolism
mitochondrial function
morphology
Morphology. Physiology
motility
Rhodamine 123
Rhodamines
Sperm Maturation
spermatozoa
Spermatozoa - metabolism
Vertebrates: reproduction
title Investigation of epididymal sperm maturation in the golden hamster
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