Quercetin, a rat intestinal and bladder carcinogen present in bracken fern (Pteridium aquilinum)
Albino noninbred weanling male and female rats were fed a basic grain diet (Group 1) or a basic diet supplemented with 33% bracken fern [BF (Group 2)] or 0.1% quercetin [purity, > 99% (Group 3)] for 58 weeks. The quantities of quercetin and kaempferol (a close structural analog) in BF as glycosid...
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Veröffentlicht in: | Cancer research (Chicago, Ill.) Ill.), 1980-10, Vol.40 (10), p.3468 |
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description | Albino noninbred weanling male and female rats were fed a basic grain diet (Group 1) or a basic diet supplemented with 33% bracken fern [BF (Group 2)] or 0.1% quercetin [purity, > 99% (Group 3)] for 58 weeks. The quantities of quercetin and kaempferol (a close structural analog) in BF as glycosides were determined to be 0.57 and 1.1 g, respectively, per kg of dried BF. Estimated mean total cumulative doses (mmol) per rat were: Group 1, quercetin, males and females < 0.03; kaempferol, males and females < 0.03; Group 2, quercetin, males 5.8, females 5.2; kaempferol, males 11.9, females 10.8; and Group 3, quercetin, males 27.8, females 25.3; kaempferol, males and females < 0.03. Growth of rats fed BF or quercetin was comparable but significantly (p < 0.01) slower after 24 weeks than that of Group 1. Mean survivals (weeks) of rats of all groups were: Group 1, 58 +/- 7 (S.D.); Group 2, 51 +/- 13; and Group 3, 56 +/- 8. They were not significantly different, although rats fed BF tended to die earlier secondary to intestinal tumor-induced intussusception and obstruction. The following incidences of intestinal or bladder neoplasms in male or female rats, respectively, were observed: Group 1, intestinal and bladder, males, 0 of 9, females, 0 of 10; Group 2, intestinal, males, 7 of 8, females, 10 of 11; bladder, males, 6 of 8, females 8 of 11; Group 3, intestinal, males, 6 of 7, females, 14 of 18; bladder, males, 2 of 7, females, 3 of 18. The histopathology of neoplasms of the 2 target organs was identical for rats of Groups 2 and 3. Multiple ileal intestinal neoplasms of rats fed quercetin included: adenoma, 4; fibroadenoma, 7; and adenocarcinoma, 9 (with mesenteric metastases, 3). The 5 bladder tumors were papillary or sessile transitional cell carcinomas. |
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The quantities of quercetin and kaempferol (a close structural analog) in BF as glycosides were determined to be 0.57 and 1.1 g, respectively, per kg of dried BF. Estimated mean total cumulative doses (mmol) per rat were: Group 1, quercetin, males and females < 0.03; kaempferol, males and females < 0.03; Group 2, quercetin, males 5.8, females 5.2; kaempferol, males 11.9, females 10.8; and Group 3, quercetin, males 27.8, females 25.3; kaempferol, males and females < 0.03. Growth of rats fed BF or quercetin was comparable but significantly (p < 0.01) slower after 24 weeks than that of Group 1. Mean survivals (weeks) of rats of all groups were: Group 1, 58 +/- 7 (S.D.); Group 2, 51 +/- 13; and Group 3, 56 +/- 8. They were not significantly different, although rats fed BF tended to die earlier secondary to intestinal tumor-induced intussusception and obstruction. The following incidences of intestinal or bladder neoplasms in male or female rats, respectively, were observed: Group 1, intestinal and bladder, males, 0 of 9, females, 0 of 10; Group 2, intestinal, males, 7 of 8, females, 10 of 11; bladder, males, 6 of 8, females 8 of 11; Group 3, intestinal, males, 6 of 7, females, 14 of 18; bladder, males, 2 of 7, females, 3 of 18. The histopathology of neoplasms of the 2 target organs was identical for rats of Groups 2 and 3. Multiple ileal intestinal neoplasms of rats fed quercetin included: adenoma, 4; fibroadenoma, 7; and adenocarcinoma, 9 (with mesenteric metastases, 3). The 5 bladder tumors were papillary or sessile transitional cell carcinomas.</description><identifier>ISSN: 0008-5472</identifier><identifier>PMID: 7438034</identifier><language>eng</language><publisher>United States</publisher><subject>Adenocarcinoma - chemically induced ; Adenocarcinoma - pathology ; Adenofibroma - chemically induced ; Adenoma - chemically induced ; Adenoma - pathology ; Animals ; Body Weight ; Carcinoma, Transitional Cell - chemically induced ; Carcinoma, Transitional Cell - pathology ; Diet ; Female ; Flavonoids - toxicity ; Intestinal Neoplasms - chemically induced ; Intestinal Neoplasms - pathology ; Male ; Plants, Toxic - analysis ; Quercetin - analysis ; Quercetin - toxicity ; Rats ; Time Factors ; Urinary Bladder Neoplasms - chemically induced ; Urinary Bladder Neoplasms - pathology</subject><ispartof>Cancer research (Chicago, Ill.), 1980-10, Vol.40 (10), p.3468</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7438034$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pamukcu, A M</creatorcontrib><creatorcontrib>Yalçiner, S</creatorcontrib><creatorcontrib>Hatcher, J F</creatorcontrib><creatorcontrib>Bryan, G T</creatorcontrib><title>Quercetin, a rat intestinal and bladder carcinogen present in bracken fern (Pteridium aquilinum)</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>Albino noninbred weanling male and female rats were fed a basic grain diet (Group 1) or a basic diet supplemented with 33% bracken fern [BF (Group 2)] or 0.1% quercetin [purity, > 99% (Group 3)] for 58 weeks. The quantities of quercetin and kaempferol (a close structural analog) in BF as glycosides were determined to be 0.57 and 1.1 g, respectively, per kg of dried BF. Estimated mean total cumulative doses (mmol) per rat were: Group 1, quercetin, males and females < 0.03; kaempferol, males and females < 0.03; Group 2, quercetin, males 5.8, females 5.2; kaempferol, males 11.9, females 10.8; and Group 3, quercetin, males 27.8, females 25.3; kaempferol, males and females < 0.03. Growth of rats fed BF or quercetin was comparable but significantly (p < 0.01) slower after 24 weeks than that of Group 1. Mean survivals (weeks) of rats of all groups were: Group 1, 58 +/- 7 (S.D.); Group 2, 51 +/- 13; and Group 3, 56 +/- 8. They were not significantly different, although rats fed BF tended to die earlier secondary to intestinal tumor-induced intussusception and obstruction. The following incidences of intestinal or bladder neoplasms in male or female rats, respectively, were observed: Group 1, intestinal and bladder, males, 0 of 9, females, 0 of 10; Group 2, intestinal, males, 7 of 8, females, 10 of 11; bladder, males, 6 of 8, females 8 of 11; Group 3, intestinal, males, 6 of 7, females, 14 of 18; bladder, males, 2 of 7, females, 3 of 18. The histopathology of neoplasms of the 2 target organs was identical for rats of Groups 2 and 3. Multiple ileal intestinal neoplasms of rats fed quercetin included: adenoma, 4; fibroadenoma, 7; and adenocarcinoma, 9 (with mesenteric metastases, 3). The 5 bladder tumors were papillary or sessile transitional cell carcinomas.</description><subject>Adenocarcinoma - chemically induced</subject><subject>Adenocarcinoma - pathology</subject><subject>Adenofibroma - chemically induced</subject><subject>Adenoma - chemically induced</subject><subject>Adenoma - pathology</subject><subject>Animals</subject><subject>Body Weight</subject><subject>Carcinoma, Transitional Cell - chemically induced</subject><subject>Carcinoma, Transitional Cell - pathology</subject><subject>Diet</subject><subject>Female</subject><subject>Flavonoids - toxicity</subject><subject>Intestinal Neoplasms - chemically induced</subject><subject>Intestinal Neoplasms - pathology</subject><subject>Male</subject><subject>Plants, Toxic - analysis</subject><subject>Quercetin - analysis</subject><subject>Quercetin - toxicity</subject><subject>Rats</subject><subject>Time Factors</subject><subject>Urinary Bladder Neoplasms - chemically induced</subject><subject>Urinary Bladder Neoplasms - pathology</subject><issn>0008-5472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1980</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNotj0tLxDAUhbNQxnH0JwhZKlhIe_NolzL4ggEVZtbjTXKj0TbWtF347604q8N3-DhwjthSCFEXSprqhJ0Ow8eMqhRqwRZGQi1ALtnry0TZ0RjTNUeeceQxjTTMjC3H5Llt0XvK3GF2MX29UeJ9poHSn8ltRvc5V4Fy4pfPI-Xo49Rx_J5iG9PUXZ2x44DtQOeHXLHd3e12_VBsnu4f1zeb4r2SYiwa5Q0RIIoGpBSl8Y2E0phahzo0GsuAKmCprQOlnQWtwFsdKuuUAtdoWLGL_91-sh35fZ9jh_lnf3gKv4AyTy4</recordid><startdate>19801001</startdate><enddate>19801001</enddate><creator>Pamukcu, A M</creator><creator>Yalçiner, S</creator><creator>Hatcher, J F</creator><creator>Bryan, G T</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>19801001</creationdate><title>Quercetin, a rat intestinal and bladder carcinogen present in bracken fern (Pteridium aquilinum)</title><author>Pamukcu, A M ; Yalçiner, S ; Hatcher, J F ; Bryan, G T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h240t-95d7ee3aa09344017d94317786f8f96a1fa5fa16bc356cb3653db6f2bc553c963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1980</creationdate><topic>Adenocarcinoma - chemically induced</topic><topic>Adenocarcinoma - pathology</topic><topic>Adenofibroma - chemically induced</topic><topic>Adenoma - chemically induced</topic><topic>Adenoma - pathology</topic><topic>Animals</topic><topic>Body Weight</topic><topic>Carcinoma, Transitional Cell - chemically induced</topic><topic>Carcinoma, Transitional Cell - pathology</topic><topic>Diet</topic><topic>Female</topic><topic>Flavonoids - toxicity</topic><topic>Intestinal Neoplasms - chemically induced</topic><topic>Intestinal Neoplasms - pathology</topic><topic>Male</topic><topic>Plants, Toxic - analysis</topic><topic>Quercetin - analysis</topic><topic>Quercetin - toxicity</topic><topic>Rats</topic><topic>Time Factors</topic><topic>Urinary Bladder Neoplasms - chemically induced</topic><topic>Urinary Bladder Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pamukcu, A M</creatorcontrib><creatorcontrib>Yalçiner, S</creatorcontrib><creatorcontrib>Hatcher, J F</creatorcontrib><creatorcontrib>Bryan, G T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pamukcu, A M</au><au>Yalçiner, S</au><au>Hatcher, J F</au><au>Bryan, G T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quercetin, a rat intestinal and bladder carcinogen present in bracken fern (Pteridium aquilinum)</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1980-10-01</date><risdate>1980</risdate><volume>40</volume><issue>10</issue><spage>3468</spage><pages>3468-</pages><issn>0008-5472</issn><abstract>Albino noninbred weanling male and female rats were fed a basic grain diet (Group 1) or a basic diet supplemented with 33% bracken fern [BF (Group 2)] or 0.1% quercetin [purity, > 99% (Group 3)] for 58 weeks. The quantities of quercetin and kaempferol (a close structural analog) in BF as glycosides were determined to be 0.57 and 1.1 g, respectively, per kg of dried BF. Estimated mean total cumulative doses (mmol) per rat were: Group 1, quercetin, males and females < 0.03; kaempferol, males and females < 0.03; Group 2, quercetin, males 5.8, females 5.2; kaempferol, males 11.9, females 10.8; and Group 3, quercetin, males 27.8, females 25.3; kaempferol, males and females < 0.03. Growth of rats fed BF or quercetin was comparable but significantly (p < 0.01) slower after 24 weeks than that of Group 1. Mean survivals (weeks) of rats of all groups were: Group 1, 58 +/- 7 (S.D.); Group 2, 51 +/- 13; and Group 3, 56 +/- 8. They were not significantly different, although rats fed BF tended to die earlier secondary to intestinal tumor-induced intussusception and obstruction. The following incidences of intestinal or bladder neoplasms in male or female rats, respectively, were observed: Group 1, intestinal and bladder, males, 0 of 9, females, 0 of 10; Group 2, intestinal, males, 7 of 8, females, 10 of 11; bladder, males, 6 of 8, females 8 of 11; Group 3, intestinal, males, 6 of 7, females, 14 of 18; bladder, males, 2 of 7, females, 3 of 18. The histopathology of neoplasms of the 2 target organs was identical for rats of Groups 2 and 3. Multiple ileal intestinal neoplasms of rats fed quercetin included: adenoma, 4; fibroadenoma, 7; and adenocarcinoma, 9 (with mesenteric metastases, 3). The 5 bladder tumors were papillary or sessile transitional cell carcinomas.</abstract><cop>United States</cop><pmid>7438034</pmid></addata></record> |
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subjects | Adenocarcinoma - chemically induced Adenocarcinoma - pathology Adenofibroma - chemically induced Adenoma - chemically induced Adenoma - pathology Animals Body Weight Carcinoma, Transitional Cell - chemically induced Carcinoma, Transitional Cell - pathology Diet Female Flavonoids - toxicity Intestinal Neoplasms - chemically induced Intestinal Neoplasms - pathology Male Plants, Toxic - analysis Quercetin - analysis Quercetin - toxicity Rats Time Factors Urinary Bladder Neoplasms - chemically induced Urinary Bladder Neoplasms - pathology |
title | Quercetin, a rat intestinal and bladder carcinogen present in bracken fern (Pteridium aquilinum) |
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