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Role of potassium channels, the sodium-potassium pump and the cytoskeleton in the control of dog sperm volume
Response to osmotic shock is an important aspect of mammalian sperm physiology. In this study we recorded volume changes of dog spermatozoa at 39, 33, and 25 °C under isotonic conditions and following hypotonic shock. Cell volume measurements were performed electronically in saline solutions of 300...
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Published in: | Theriogenology 2004, Vol.61 (1), p.35-54 |
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description | Response to osmotic shock is an important aspect of mammalian sperm physiology. In this study we recorded volume changes of dog spermatozoa at 39, 33, and 25
°C under isotonic conditions and following hypotonic shock. Cell volume measurements were performed electronically in saline solutions of 300 and 150
mOsmol
kg
−1, and Percoll-washed preparations were compared with unwashed samples. The involvement of potassium channels in volume control was tested by treatment with quinine, while the involvement of the plasma membrane Na
+-K
+ pump was tested by treatment with ouabain. The role of the cytoskeleton was investigated by treatment with colchicine and cytochalasin D. The number of cell populations observed varied with temperature and tonicity. In both types of sperm preparations, between two and three populations were present under isotonic conditions at 25
°C whereas at 39 and 33
°C only one population was detected. Hypotonic stress at the higher temperatures caused the single population to swell, whereas at 25
°C it resulted in a population of cells whose modal volume was similar to that of the middle isotonic sub-population. Both quinine and the cytoskeletal inhibitors markedly increased swelling both under hypotonic conditions at 39
°C and under isotonic conditions at 25
°C. However, little or no effect of ouabain was observed. We conclude that in dog spermatozoa swelling in response to hypotonic conditions is minimised through the activity of potassium channels and the presence of an intact cytoskeletal network. Under isotonic conditions at 25
°C, a considerable proportion of the sperm population is already swollen; this swelling varies between individual males and appears to be due to lowered cytoskeletal and potassium channel activity. |
doi_str_mv | 10.1016/S0093-691X(03)00184-5 |
format | article |
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°C under isotonic conditions and following hypotonic shock. Cell volume measurements were performed electronically in saline solutions of 300 and 150
mOsmol
kg
−1, and Percoll-washed preparations were compared with unwashed samples. The involvement of potassium channels in volume control was tested by treatment with quinine, while the involvement of the plasma membrane Na
+-K
+ pump was tested by treatment with ouabain. The role of the cytoskeleton was investigated by treatment with colchicine and cytochalasin D. The number of cell populations observed varied with temperature and tonicity. In both types of sperm preparations, between two and three populations were present under isotonic conditions at 25
°C whereas at 39 and 33
°C only one population was detected. Hypotonic stress at the higher temperatures caused the single population to swell, whereas at 25
°C it resulted in a population of cells whose modal volume was similar to that of the middle isotonic sub-population. Both quinine and the cytoskeletal inhibitors markedly increased swelling both under hypotonic conditions at 39
°C and under isotonic conditions at 25
°C. However, little or no effect of ouabain was observed. We conclude that in dog spermatozoa swelling in response to hypotonic conditions is minimised through the activity of potassium channels and the presence of an intact cytoskeletal network. Under isotonic conditions at 25
°C, a considerable proportion of the sperm population is already swollen; this swelling varies between individual males and appears to be due to lowered cytoskeletal and potassium channel activity.</description><identifier>ISSN: 0093-691X</identifier><identifier>EISSN: 1879-3231</identifier><identifier>DOI: 10.1016/S0093-691X(03)00184-5</identifier><identifier>PMID: 14643860</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>ambient temperature ; animal reproduction ; Animals ; Cell Size ; Cell volume ; Colchicine - pharmacology ; culture media ; Cytochalasin D - pharmacology ; Cytoskeleton ; Cytoskeleton - drug effects ; Cytoskeleton - physiology ; Dogs ; Hypotonic Solutions ; Ion transport ; ionic strength ; Male ; osmoregulation ; Osmotic Pressure ; Osmotic schock ; Ouabain - pharmacology ; Potassium Channel Blockers - pharmacology ; potassium channels ; Potassium Channels - physiology ; Quinine - pharmacology ; Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors ; Sodium-Potassium-Exchanging ATPase - physiology ; spermatozoa ; Spermatozoa - cytology ; Temperature ; volume</subject><ispartof>Theriogenology, 2004, Vol.61 (1), p.35-54</ispartof><rights>2003 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-19d5896b9a7f379b2f548a6c7730f52665960b37bc7618629d14092c38f72bcd3</citedby><cites>FETCH-LOGICAL-c451t-19d5896b9a7f379b2f548a6c7730f52665960b37bc7618629d14092c38f72bcd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14643860$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Petrunkina, A.M</creatorcontrib><creatorcontrib>Radcke, S</creatorcontrib><creatorcontrib>Günzel-Apel, A.-R</creatorcontrib><creatorcontrib>Harrison, R.A.P</creatorcontrib><creatorcontrib>Töpfer-Petersen, E</creatorcontrib><title>Role of potassium channels, the sodium-potassium pump and the cytoskeleton in the control of dog sperm volume</title><title>Theriogenology</title><addtitle>Theriogenology</addtitle><description>Response to osmotic shock is an important aspect of mammalian sperm physiology. In this study we recorded volume changes of dog spermatozoa at 39, 33, and 25
°C under isotonic conditions and following hypotonic shock. Cell volume measurements were performed electronically in saline solutions of 300 and 150
mOsmol
kg
−1, and Percoll-washed preparations were compared with unwashed samples. The involvement of potassium channels in volume control was tested by treatment with quinine, while the involvement of the plasma membrane Na
+-K
+ pump was tested by treatment with ouabain. The role of the cytoskeleton was investigated by treatment with colchicine and cytochalasin D. The number of cell populations observed varied with temperature and tonicity. In both types of sperm preparations, between two and three populations were present under isotonic conditions at 25
°C whereas at 39 and 33
°C only one population was detected. Hypotonic stress at the higher temperatures caused the single population to swell, whereas at 25
°C it resulted in a population of cells whose modal volume was similar to that of the middle isotonic sub-population. Both quinine and the cytoskeletal inhibitors markedly increased swelling both under hypotonic conditions at 39
°C and under isotonic conditions at 25
°C. However, little or no effect of ouabain was observed. We conclude that in dog spermatozoa swelling in response to hypotonic conditions is minimised through the activity of potassium channels and the presence of an intact cytoskeletal network. Under isotonic conditions at 25
°C, a considerable proportion of the sperm population is already swollen; this swelling varies between individual males and appears to be due to lowered cytoskeletal and potassium channel activity.</description><subject>ambient temperature</subject><subject>animal reproduction</subject><subject>Animals</subject><subject>Cell Size</subject><subject>Cell volume</subject><subject>Colchicine - pharmacology</subject><subject>culture media</subject><subject>Cytochalasin D - pharmacology</subject><subject>Cytoskeleton</subject><subject>Cytoskeleton - drug effects</subject><subject>Cytoskeleton - physiology</subject><subject>Dogs</subject><subject>Hypotonic Solutions</subject><subject>Ion transport</subject><subject>ionic strength</subject><subject>Male</subject><subject>osmoregulation</subject><subject>Osmotic Pressure</subject><subject>Osmotic schock</subject><subject>Ouabain - pharmacology</subject><subject>Potassium Channel Blockers - pharmacology</subject><subject>potassium channels</subject><subject>Potassium Channels - physiology</subject><subject>Quinine - pharmacology</subject><subject>Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors</subject><subject>Sodium-Potassium-Exchanging ATPase - physiology</subject><subject>spermatozoa</subject><subject>Spermatozoa - cytology</subject><subject>Temperature</subject><subject>volume</subject><issn>0093-691X</issn><issn>1879-3231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqFkM1q3TAQRkVoSW7TPkJSrUILdauxLMlahRL6B4FA0kB3QpbGiVrbciQ7kLev7_WlWXY1MHPmm-EQcgLsIzCQn24Y07yQGn69Y_w9Y1BXhTggG6iVLnjJ4QXZ_EOOyKucfzPGuJRwSI6gkhWvJduQ_jp2SGNLxzjZnMPcU3dvhwG7_IFO90hz9EuzeB6Pcz9SO_jd1D1NMf_BDqc40DCsvThMKXbbUB_vaB4x9fQxdnOPr8nL1nYZ3-zrMbn9-uXnxffi8urbj4vPl4WrBEwFaC9qLRttVcuVbspWVLWVTinOWlFKKbRkDVeNUxJqWWoPFdOl43WrysZ5fkzO1twxxYcZ82T6kB12nR0wztkoEIKLGhZQrKBLMeeErRlT6G16MsDM1rPZeTZbiYZxs_NsxLJ3uj8wNz3656292AV4uwKtjcbepZDN7U3JgG_jVKXlQpyvxKIaHwMmk13AwaEPCd1kfAz_eeIv_CeXAA</recordid><startdate>2004</startdate><enddate>2004</enddate><creator>Petrunkina, A.M</creator><creator>Radcke, S</creator><creator>Günzel-Apel, A.-R</creator><creator>Harrison, R.A.P</creator><creator>Töpfer-Petersen, E</creator><general>Elsevier Inc</general><scope>FBQ</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>2004</creationdate><title>Role of potassium channels, the sodium-potassium pump and the cytoskeleton in the control of dog sperm volume</title><author>Petrunkina, A.M ; Radcke, S ; Günzel-Apel, A.-R ; Harrison, R.A.P ; Töpfer-Petersen, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-19d5896b9a7f379b2f548a6c7730f52665960b37bc7618629d14092c38f72bcd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>ambient temperature</topic><topic>animal reproduction</topic><topic>Animals</topic><topic>Cell Size</topic><topic>Cell volume</topic><topic>Colchicine - pharmacology</topic><topic>culture media</topic><topic>Cytochalasin D - pharmacology</topic><topic>Cytoskeleton</topic><topic>Cytoskeleton - drug effects</topic><topic>Cytoskeleton - physiology</topic><topic>Dogs</topic><topic>Hypotonic Solutions</topic><topic>Ion transport</topic><topic>ionic strength</topic><topic>Male</topic><topic>osmoregulation</topic><topic>Osmotic Pressure</topic><topic>Osmotic schock</topic><topic>Ouabain - pharmacology</topic><topic>Potassium Channel Blockers - pharmacology</topic><topic>potassium channels</topic><topic>Potassium Channels - physiology</topic><topic>Quinine - pharmacology</topic><topic>Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors</topic><topic>Sodium-Potassium-Exchanging ATPase - physiology</topic><topic>spermatozoa</topic><topic>Spermatozoa - cytology</topic><topic>Temperature</topic><topic>volume</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Petrunkina, A.M</creatorcontrib><creatorcontrib>Radcke, S</creatorcontrib><creatorcontrib>Günzel-Apel, A.-R</creatorcontrib><creatorcontrib>Harrison, R.A.P</creatorcontrib><creatorcontrib>Töpfer-Petersen, E</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Theriogenology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Petrunkina, A.M</au><au>Radcke, S</au><au>Günzel-Apel, A.-R</au><au>Harrison, R.A.P</au><au>Töpfer-Petersen, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of potassium channels, the sodium-potassium pump and the cytoskeleton in the control of dog sperm volume</atitle><jtitle>Theriogenology</jtitle><addtitle>Theriogenology</addtitle><date>2004</date><risdate>2004</risdate><volume>61</volume><issue>1</issue><spage>35</spage><epage>54</epage><pages>35-54</pages><issn>0093-691X</issn><eissn>1879-3231</eissn><abstract>Response to osmotic shock is an important aspect of mammalian sperm physiology. In this study we recorded volume changes of dog spermatozoa at 39, 33, and 25
°C under isotonic conditions and following hypotonic shock. Cell volume measurements were performed electronically in saline solutions of 300 and 150
mOsmol
kg
−1, and Percoll-washed preparations were compared with unwashed samples. The involvement of potassium channels in volume control was tested by treatment with quinine, while the involvement of the plasma membrane Na
+-K
+ pump was tested by treatment with ouabain. The role of the cytoskeleton was investigated by treatment with colchicine and cytochalasin D. The number of cell populations observed varied with temperature and tonicity. In both types of sperm preparations, between two and three populations were present under isotonic conditions at 25
°C whereas at 39 and 33
°C only one population was detected. Hypotonic stress at the higher temperatures caused the single population to swell, whereas at 25
°C it resulted in a population of cells whose modal volume was similar to that of the middle isotonic sub-population. Both quinine and the cytoskeletal inhibitors markedly increased swelling both under hypotonic conditions at 39
°C and under isotonic conditions at 25
°C. However, little or no effect of ouabain was observed. We conclude that in dog spermatozoa swelling in response to hypotonic conditions is minimised through the activity of potassium channels and the presence of an intact cytoskeletal network. Under isotonic conditions at 25
°C, a considerable proportion of the sperm population is already swollen; this swelling varies between individual males and appears to be due to lowered cytoskeletal and potassium channel activity.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>14643860</pmid><doi>10.1016/S0093-691X(03)00184-5</doi><tpages>20</tpages></addata></record> |
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subjects | ambient temperature animal reproduction Animals Cell Size Cell volume Colchicine - pharmacology culture media Cytochalasin D - pharmacology Cytoskeleton Cytoskeleton - drug effects Cytoskeleton - physiology Dogs Hypotonic Solutions Ion transport ionic strength Male osmoregulation Osmotic Pressure Osmotic schock Ouabain - pharmacology Potassium Channel Blockers - pharmacology potassium channels Potassium Channels - physiology Quinine - pharmacology Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors Sodium-Potassium-Exchanging ATPase - physiology spermatozoa Spermatozoa - cytology Temperature volume |
title | Role of potassium channels, the sodium-potassium pump and the cytoskeleton in the control of dog sperm volume |
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