Effect of green tea on some biochemical parameters in rats treated with AFB₁-CCI₄ as cancer inducers (Record no. 36960)
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| 000 -LEADER | |
|---|---|
| fixed length control field | 04199cab a2200337Ia 45 0 |
| 001 - CONTROL NUMBER | |
| control field | u159355 |
| 003 - CONTROL NUMBER IDENTIFIER | |
| control field | SIRSI |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 100316s2008 ua ss b eng d |
| 040 ## - CATALOGING SOURCE | |
| Original cataloging agency | EAL |
| 041 ## - LANGUAGE CODE | |
| Language code of text/sound track or separate title | eng |
| Language code of summary or abstract | ara |
| 090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN) | |
| Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) | ART JBCES V3 No1 II 6 |
| 100 1# - MAIN ENTRY--PERSONAL NAME | |
| Personal name | El-Shafei, Sally M.A. |
| 240 10 - UNIFORM TITLE | |
| Uniform title | Journal of biological chemistry and environmental sciences, 2008 v. 3 (1) |
| Number of part/section of a work | Part II |
| Medium | [electronic resource]. |
| 245 10 - TITLE STATEMENT | |
| Title | Effect of green tea on some biochemical parameters in rats treated with AFB₁-CCI₄ as cancer inducers |
| Medium | [electronic resource]. |
| 246 15 - VARYING FORM OF TITLE | |
| Title proper/short title | تأثير الشاي الأخضر على بعض الوظائف الحيوية في فئران التجارب المعاملة بالأفلاتوكسين ورابع كلوريد الكربون. |
| 300 ## - PHYSICAL DESCRIPTION | |
| Extent | p.319-342 |
| 504 ## - BIBLIOGRAPHY, ETC. NOTE | |
| Bibliography, etc. note | Includes reference. |
| 520 ## - SUMMARY, ETC. | |
| Summary, etc. | In the present work 160 male albino rats were randomly divided into four groups (40 rats each): Group I (control group), Group II (AFBI-CCI4), Group III (AFBI-CCI4, followed by green tea extract (GTE) as the sole source of drinking fluid and Group IV GTE followed by AFB₁-CCI₄. The effect of GTE on the relative weight of liver and kidney, and some biochemical parameters were determined in rats treated with AFB₁-CCI₄. Treating rats with AFB₁+CCI₄ (Group II) for 12 weeks increased the relative weight of liver together with kidney compared with those of untreated rats (Group I, control). The enlargement of these organ stended to decrease by the end of the experiment (16 weeks), but still higher than those of control. The harmful effect of AFB₁+CCI₄ on therelative weight of the above mentioned organs, has been markedly remediated with applying GTE either after or before applying AFB₁-CCI₄. Changes in ALT level in serum of rats of Group III was similar to those recorded in Group II during the first 12 week, but tend to decrease sharply to attend the levels recorded in serum of the animal of control group by the end of week 16. Treating rats with GTE either after or before AFBl+CCI4 treatments depressed the level of ALT to values similar to those recorded in control animals (Group I). The changes in AST in serum of rats of the four groups during the experimental period were similar to those demonstrated for ALT. The serum total bilirubin in rats treated with AFB₁ followed by CCI₄ Group II and III was significantly higher than those recorded for control animals especially during the first 12 weeks of the experiment. Treatment with GTE before AFB₁-CCI₄ revealed total bilirubin levels very close to those observed for the control animals during the whole experemintal period. Results indicated that both urea and creatinine (except for the first 2 weeks), increased steadily in rats treated with only AFB₁+CCI₄ (Group II and III) for 12 weeks, then their concentration tend to decrease during the last four weeks of the experiment. Treating rats with GTE before AFB₁+CCI₄ treatment (Group IV) decreased the elevation in both urea and creatinine concentration throughout the experimental period (16 weeks). Pretreating with GTE seemed to be more effective as chemopreventive agents (Group IV) rather than post-treating (after AFB₁+CCI₄) (Group III). Data reveal that treating rats with AFB₁+CCI₄ (GroupII) resulted in gradual increases in GSH up to the twelfth week, and then it tended to decrease. On the other hand, GST behaved in opposite trend shown in case of GSH. Post-treating rats with GTE exerted such decreases in GSH values, but to less extent compared with GTE pretreated rats, which seemed to be more effective than post-treating GTE did. |
| 546 ## - LANGUAGE NOTE | |
| Language note | Summary in Arabic. |
| 596 ## - | |
| -- | 1 |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Aflatoxins |
| General subdivision | Toxicology. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Green tea |
| General subdivision | Therapeutic use |
| -- | Testing. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Cancer |
| General subdivision | Research. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Rats |
| General subdivision | Diseases. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Rats |
| General subdivision | Physiology |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Abd El-Kader, Salah M. |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Turk, Salah A. |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | El-Moris, El-Morsi A. |
| 773 0# - HOST ITEM ENTRY | |
| Title | Journal of Biological Chemistry and Environmental Sciences. |
| Related parts | 2008.v.3(1)II |
| International Standard Serial Number | 1687-5478 |
| Control subfield | nnas |
| Record control number | u159296 |
| 856 40 - ELECTRONIC LOCATION AND ACCESS | |
| Uniform Resource Identifier | <a href="http://nile.enal.sci.eg/EALE/2008/JBCES/308/1/II/319.pdf">http://nile.enal.sci.eg/EALE/2008/JBCES/308/1/II/319.pdf</a> |
| Public note | Full Text Article. |
| 942 ## - ADDED ENTRY ELEMENTS (KOHA) | |
| Koha item type | Articles |
| Source of classification or shelving scheme | Library of Congress Classification |
No items available.