Sucralose: lack of effects on sperm glycolysis and reproduction in the rat
Certain chlorine-substituted sugars with chemical similarities to sucralose have been demonstrated previously to diminish or inhibit sperm glycolysis and fertility in the rat ( Ford and Waites, 1978a). In order to investigate this potential for sucralose, epididymal spermatozoa were recovered from r...
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creator | Kille, J.W. Ford, W.C.L. McAnulty, P. Tesh, J.M. Ross, F.W. Willoughby, C.R. |
description | Certain chlorine-substituted sugars with chemical similarities to sucralose have been demonstrated previously to diminish or inhibit sperm glycolysis and fertility in the rat (
Ford and Waites, 1978a). In order to investigate this potential for sucralose, epididymal spermatozoa were recovered from rats exposed
in vivo to oral doses of one of three of these substituted sugars: 6-chloroglucose (6-CG, 24
mg/kg/day, positive control), sucralose (500
mg/kg/day, over 300 times the expected human daily intake), or a 6′-substituted isomer of sucralose, trichloro de-oxy sucrose (TCDS, 100
mg/kg/day, a potential trace impurity in commercial sucralose); distilled water served as the negative control. After incubation of the spermatozoa with
d-[U-
14C] glucose, measurements of
14CO
2 and of ATP content showed no impairment of the glycolytic ability of spermatozoa in any of the groups except for a marked inhibition for those exposed to 6-CG, the positive control. In order to determine whether other parameters of reproduction and fertility could be affected, reproductive endpoints were examined following oral exposure of male and female rats to sucralose. Sucralose was fed in the diet at concentrations of 0, 0.3, 1.0 and 3.0% (approx. 100, 365 and 1150 times the EDI) to groups of 30 male and 30 female rats for 10 weeks prior to mating, and continued through two subsequent generations until weaning of the F
2 pups. Two litters were produced per generation. Food consumption and weight gain in the F
0 and F
1 generations were depressed in all sucralose groups before mating and in all four litters prior to weaning. The decrease in initial average weight for newborn pups probably reflects the increased litter sizes noted for sucralose-treated groups and the reduced food consumption of the dams during gestation and lactation. The latter is a result primarily of the unpalatability of sucralose to rats (
McNeil, 1987). Caecal enlargement (a common animal response to large doses of indigestible material) occurred in both the F
0 and F
1 parents. Increased kidney weights, possibly associated with increased water intake, were observed primarily among animals receiving 3% sucralose (no renal histopathology has been detected). Decreased thymus weights occurred in F
1 males and in both F
1 and F
2 females at the 3% level. Subsequent studies specifically designed to investigate the potential for adverse immune system effects of sucralose (
McNeil, 1987) showed no adverse effects. Thes |
doi_str_mv | 10.1016/S0278-6915(00)00025-9 |
format | Article |
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Ford and Waites, 1978a). In order to investigate this potential for sucralose, epididymal spermatozoa were recovered from rats exposed
in vivo to oral doses of one of three of these substituted sugars: 6-chloroglucose (6-CG, 24
mg/kg/day, positive control), sucralose (500
mg/kg/day, over 300 times the expected human daily intake), or a 6′-substituted isomer of sucralose, trichloro de-oxy sucrose (TCDS, 100
mg/kg/day, a potential trace impurity in commercial sucralose); distilled water served as the negative control. After incubation of the spermatozoa with
d-[U-
14C] glucose, measurements of
14CO
2 and of ATP content showed no impairment of the glycolytic ability of spermatozoa in any of the groups except for a marked inhibition for those exposed to 6-CG, the positive control. In order to determine whether other parameters of reproduction and fertility could be affected, reproductive endpoints were examined following oral exposure of male and female rats to sucralose. Sucralose was fed in the diet at concentrations of 0, 0.3, 1.0 and 3.0% (approx. 100, 365 and 1150 times the EDI) to groups of 30 male and 30 female rats for 10 weeks prior to mating, and continued through two subsequent generations until weaning of the F
2 pups. Two litters were produced per generation. Food consumption and weight gain in the F
0 and F
1 generations were depressed in all sucralose groups before mating and in all four litters prior to weaning. The decrease in initial average weight for newborn pups probably reflects the increased litter sizes noted for sucralose-treated groups and the reduced food consumption of the dams during gestation and lactation. The latter is a result primarily of the unpalatability of sucralose to rats (
McNeil, 1987). Caecal enlargement (a common animal response to large doses of indigestible material) occurred in both the F
0 and F
1 parents. Increased kidney weights, possibly associated with increased water intake, were observed primarily among animals receiving 3% sucralose (no renal histopathology has been detected). Decreased thymus weights occurred in F
1 males and in both F
1 and F
2 females at the 3% level. Subsequent studies specifically designed to investigate the potential for adverse immune system effects of sucralose (
McNeil, 1987) showed no adverse effects. These findings are consistent with investigations by others showing that decreases in thymus weights occur in young rats in response to stressful conditions associated with reductions in weight gain. All reproductive indices (oestrous cycles, mating behaviour, fertility, gestation, maternal and foetal viability, foetal development, parturition, pup maturation and lactation) were comparable between the control and sucralose-treated groups. We conclude from these results that sucralose has no effect on sperm glycolysis or on male or female reproductive performance in the rat.</description><identifier>ISSN: 0278-6915</identifier><identifier>EISSN: 1873-6351</identifier><identifier>DOI: 10.1016/S0278-6915(00)00025-9</identifier><identifier>PMID: 10882815</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>6-chlorosugars ; Adenosine Triphosphate - analysis ; Animals ; Animals, Newborn ; artificial sweeteners ; Body Weight - drug effects ; Carbon Dioxide - metabolism ; disaccharides ; Drinking - drug effects ; Eating - drug effects ; Female ; Fluorometry ; Glucose - metabolism ; Glycolysis - drug effects ; Glycolysis - physiology ; Litter Size - drug effects ; Male ; monosaccharides ; Random Allocation ; rat reproduction ; Rats ; Rats, Sprague-Dawley ; Reproduction - drug effects ; Reproduction - physiology ; Scintillation Counting ; Single-Blind Method ; sperm glycolysis ; Spermatozoa - drug effects ; Spermatozoa - metabolism ; sucralose ; Sucrose - analogs & derivatives ; Sucrose - toxicity ; Sweetening Agents - toxicity</subject><ispartof>Food and chemical toxicology, 2000-01, Vol.38, p.19-29</ispartof><rights>2000 Elsevier Science Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-a9fdb10c718ea3155fca4b3e2875639af4a0b422e91cb17ca84fc35c84fbafa93</citedby><cites>FETCH-LOGICAL-c392t-a9fdb10c718ea3155fca4b3e2875639af4a0b422e91cb17ca84fc35c84fbafa93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0278-6915(00)00025-9$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10882815$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kille, J.W.</creatorcontrib><creatorcontrib>Ford, W.C.L.</creatorcontrib><creatorcontrib>McAnulty, P.</creatorcontrib><creatorcontrib>Tesh, J.M.</creatorcontrib><creatorcontrib>Ross, F.W.</creatorcontrib><creatorcontrib>Willoughby, C.R.</creatorcontrib><title>Sucralose: lack of effects on sperm glycolysis and reproduction in the rat</title><title>Food and chemical toxicology</title><addtitle>Food Chem Toxicol</addtitle><description>Certain chlorine-substituted sugars with chemical similarities to sucralose have been demonstrated previously to diminish or inhibit sperm glycolysis and fertility in the rat (
Ford and Waites, 1978a). In order to investigate this potential for sucralose, epididymal spermatozoa were recovered from rats exposed
in vivo to oral doses of one of three of these substituted sugars: 6-chloroglucose (6-CG, 24
mg/kg/day, positive control), sucralose (500
mg/kg/day, over 300 times the expected human daily intake), or a 6′-substituted isomer of sucralose, trichloro de-oxy sucrose (TCDS, 100
mg/kg/day, a potential trace impurity in commercial sucralose); distilled water served as the negative control. After incubation of the spermatozoa with
d-[U-
14C] glucose, measurements of
14CO
2 and of ATP content showed no impairment of the glycolytic ability of spermatozoa in any of the groups except for a marked inhibition for those exposed to 6-CG, the positive control. In order to determine whether other parameters of reproduction and fertility could be affected, reproductive endpoints were examined following oral exposure of male and female rats to sucralose. Sucralose was fed in the diet at concentrations of 0, 0.3, 1.0 and 3.0% (approx. 100, 365 and 1150 times the EDI) to groups of 30 male and 30 female rats for 10 weeks prior to mating, and continued through two subsequent generations until weaning of the F
2 pups. Two litters were produced per generation. Food consumption and weight gain in the F
0 and F
1 generations were depressed in all sucralose groups before mating and in all four litters prior to weaning. The decrease in initial average weight for newborn pups probably reflects the increased litter sizes noted for sucralose-treated groups and the reduced food consumption of the dams during gestation and lactation. The latter is a result primarily of the unpalatability of sucralose to rats (
McNeil, 1987). Caecal enlargement (a common animal response to large doses of indigestible material) occurred in both the F
0 and F
1 parents. Increased kidney weights, possibly associated with increased water intake, were observed primarily among animals receiving 3% sucralose (no renal histopathology has been detected). Decreased thymus weights occurred in F
1 males and in both F
1 and F
2 females at the 3% level. Subsequent studies specifically designed to investigate the potential for adverse immune system effects of sucralose (
McNeil, 1987) showed no adverse effects. These findings are consistent with investigations by others showing that decreases in thymus weights occur in young rats in response to stressful conditions associated with reductions in weight gain. All reproductive indices (oestrous cycles, mating behaviour, fertility, gestation, maternal and foetal viability, foetal development, parturition, pup maturation and lactation) were comparable between the control and sucralose-treated groups. We conclude from these results that sucralose has no effect on sperm glycolysis or on male or female reproductive performance in the rat.</description><subject>6-chlorosugars</subject><subject>Adenosine Triphosphate - analysis</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>artificial sweeteners</subject><subject>Body Weight - drug effects</subject><subject>Carbon Dioxide - metabolism</subject><subject>disaccharides</subject><subject>Drinking - drug effects</subject><subject>Eating - drug effects</subject><subject>Female</subject><subject>Fluorometry</subject><subject>Glucose - metabolism</subject><subject>Glycolysis - drug effects</subject><subject>Glycolysis - physiology</subject><subject>Litter Size - drug effects</subject><subject>Male</subject><subject>monosaccharides</subject><subject>Random Allocation</subject><subject>rat reproduction</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reproduction - drug effects</subject><subject>Reproduction - physiology</subject><subject>Scintillation Counting</subject><subject>Single-Blind Method</subject><subject>sperm glycolysis</subject><subject>Spermatozoa - drug effects</subject><subject>Spermatozoa - metabolism</subject><subject>sucralose</subject><subject>Sucrose - analogs & derivatives</subject><subject>Sucrose - toxicity</subject><subject>Sweetening Agents - toxicity</subject><issn>0278-6915</issn><issn>1873-6351</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkD1PwzAQhi0EoqXwE0CeEAwBO4ljhwWhik9VYijMluOcwZDGxU6Q-u9xmwqxMb3Lc_fePQgdU3JBCS0u5yTlIilKys4IOSeEpCwpd9CYCp4lRcboLhr_IiN0EMJHhDjlxT4aUSJEKigbo6d5r71qXIAr3Cj9iZ3BYAzoLmDX4rAEv8BvzUq7ZhVswKqtsYeld3WvOxsJ2-LuHbBX3SHaM6oJcLTNCXq9u32ZPiSz5_vH6c0s0VmZdokqTV1RojkVoDLKmNEqrzJIBWdFViqTK1LlaQol1RXlWonc6IzpGJUyqswm6HTYG6_46iF0cmGDhqZRLbg-SMoZEyQnEWQDqL0LwYORS28Xyq8kJXItUW4kyrUhSYjcSJTrgpNtQV8toP4zNViLwPUAQHzz24KXQVtoNdTWR3Oydvafih-IfoHg</recordid><startdate>20000101</startdate><enddate>20000101</enddate><creator>Kille, J.W.</creator><creator>Ford, W.C.L.</creator><creator>McAnulty, P.</creator><creator>Tesh, J.M.</creator><creator>Ross, F.W.</creator><creator>Willoughby, C.R.</creator><general>Elsevier Ltd</general><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>7U7</scope><scope>C1K</scope></search><sort><creationdate>20000101</creationdate><title>Sucralose: lack of effects on sperm glycolysis and reproduction in the rat</title><author>Kille, J.W. ; Ford, W.C.L. ; McAnulty, P. ; Tesh, J.M. ; Ross, F.W. ; Willoughby, C.R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-a9fdb10c718ea3155fca4b3e2875639af4a0b422e91cb17ca84fc35c84fbafa93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>6-chlorosugars</topic><topic>Adenosine Triphosphate - analysis</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>artificial sweeteners</topic><topic>Body Weight - drug effects</topic><topic>Carbon Dioxide - metabolism</topic><topic>disaccharides</topic><topic>Drinking - drug effects</topic><topic>Eating - drug effects</topic><topic>Female</topic><topic>Fluorometry</topic><topic>Glucose - metabolism</topic><topic>Glycolysis - drug effects</topic><topic>Glycolysis - physiology</topic><topic>Litter Size - drug effects</topic><topic>Male</topic><topic>monosaccharides</topic><topic>Random Allocation</topic><topic>rat reproduction</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reproduction - drug effects</topic><topic>Reproduction - physiology</topic><topic>Scintillation Counting</topic><topic>Single-Blind Method</topic><topic>sperm glycolysis</topic><topic>Spermatozoa - drug effects</topic><topic>Spermatozoa - metabolism</topic><topic>sucralose</topic><topic>Sucrose - analogs & derivatives</topic><topic>Sucrose - toxicity</topic><topic>Sweetening Agents - toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kille, J.W.</creatorcontrib><creatorcontrib>Ford, W.C.L.</creatorcontrib><creatorcontrib>McAnulty, P.</creatorcontrib><creatorcontrib>Tesh, J.M.</creatorcontrib><creatorcontrib>Ross, F.W.</creatorcontrib><creatorcontrib>Willoughby, C.R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Food and chemical toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kille, J.W.</au><au>Ford, W.C.L.</au><au>McAnulty, P.</au><au>Tesh, J.M.</au><au>Ross, F.W.</au><au>Willoughby, C.R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sucralose: lack of effects on sperm glycolysis and reproduction in the rat</atitle><jtitle>Food and chemical toxicology</jtitle><addtitle>Food Chem Toxicol</addtitle><date>2000-01-01</date><risdate>2000</risdate><volume>38</volume><spage>19</spage><epage>29</epage><pages>19-29</pages><issn>0278-6915</issn><eissn>1873-6351</eissn><abstract>Certain chlorine-substituted sugars with chemical similarities to sucralose have been demonstrated previously to diminish or inhibit sperm glycolysis and fertility in the rat (
Ford and Waites, 1978a). In order to investigate this potential for sucralose, epididymal spermatozoa were recovered from rats exposed
in vivo to oral doses of one of three of these substituted sugars: 6-chloroglucose (6-CG, 24
mg/kg/day, positive control), sucralose (500
mg/kg/day, over 300 times the expected human daily intake), or a 6′-substituted isomer of sucralose, trichloro de-oxy sucrose (TCDS, 100
mg/kg/day, a potential trace impurity in commercial sucralose); distilled water served as the negative control. After incubation of the spermatozoa with
d-[U-
14C] glucose, measurements of
14CO
2 and of ATP content showed no impairment of the glycolytic ability of spermatozoa in any of the groups except for a marked inhibition for those exposed to 6-CG, the positive control. In order to determine whether other parameters of reproduction and fertility could be affected, reproductive endpoints were examined following oral exposure of male and female rats to sucralose. Sucralose was fed in the diet at concentrations of 0, 0.3, 1.0 and 3.0% (approx. 100, 365 and 1150 times the EDI) to groups of 30 male and 30 female rats for 10 weeks prior to mating, and continued through two subsequent generations until weaning of the F
2 pups. Two litters were produced per generation. Food consumption and weight gain in the F
0 and F
1 generations were depressed in all sucralose groups before mating and in all four litters prior to weaning. The decrease in initial average weight for newborn pups probably reflects the increased litter sizes noted for sucralose-treated groups and the reduced food consumption of the dams during gestation and lactation. The latter is a result primarily of the unpalatability of sucralose to rats (
McNeil, 1987). Caecal enlargement (a common animal response to large doses of indigestible material) occurred in both the F
0 and F
1 parents. Increased kidney weights, possibly associated with increased water intake, were observed primarily among animals receiving 3% sucralose (no renal histopathology has been detected). Decreased thymus weights occurred in F
1 males and in both F
1 and F
2 females at the 3% level. Subsequent studies specifically designed to investigate the potential for adverse immune system effects of sucralose (
McNeil, 1987) showed no adverse effects. These findings are consistent with investigations by others showing that decreases in thymus weights occur in young rats in response to stressful conditions associated with reductions in weight gain. All reproductive indices (oestrous cycles, mating behaviour, fertility, gestation, maternal and foetal viability, foetal development, parturition, pup maturation and lactation) were comparable between the control and sucralose-treated groups. We conclude from these results that sucralose has no effect on sperm glycolysis or on male or female reproductive performance in the rat.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>10882815</pmid><doi>10.1016/S0278-6915(00)00025-9</doi><tpages>11</tpages></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | 6-chlorosugars Adenosine Triphosphate - analysis Animals Animals, Newborn artificial sweeteners Body Weight - drug effects Carbon Dioxide - metabolism disaccharides Drinking - drug effects Eating - drug effects Female Fluorometry Glucose - metabolism Glycolysis - drug effects Glycolysis - physiology Litter Size - drug effects Male monosaccharides Random Allocation rat reproduction Rats Rats, Sprague-Dawley Reproduction - drug effects Reproduction - physiology Scintillation Counting Single-Blind Method sperm glycolysis Spermatozoa - drug effects Spermatozoa - metabolism sucralose Sucrose - analogs & derivatives Sucrose - toxicity Sweetening Agents - toxicity |
title | Sucralose: lack of effects on sperm glycolysis and reproduction in the rat |
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