Annatto (Bixa orellana) δ-TCT supplementation protection against embryonic malformations through alterations in PI3K/akt-cyclin D1 pathway
Protective action by annatto-derived delta-tocotrienol (δ-TCT) and soy-derived alpha-tocopherol (α-TOC) through the regulation of the PI3K/Akt-cyclin D1 pathway against nicotine-induced DNA damage is the focus of the present study. Nicotine, which has been widely reported to have numerous adverse ef...
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2019
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2-s2.0-85059912784 Mutalip S.S.M.; Rajikin M.H.; Rahim S.A.; Khan N.M.N. Annatto (Bixa orellana) δ-TCT supplementation protection against embryonic malformations through alterations in PI3K/akt-cyclin D1 pathway 2019 Biomolecules 9 1 10.3390/biom9010019 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85059912784&doi=10.3390%2fbiom9010019&partnerID=40&md5=8d6f8f1938a40a6aab1e17e84362d5db Protective action by annatto-derived delta-tocotrienol (δ-TCT) and soy-derived alpha-tocopherol (α-TOC) through the regulation of the PI3K/Akt-cyclin D1 pathway against nicotine-induced DNA damage is the focus of the present study. Nicotine, which has been widely reported to have numerous adverse effects on the reproductive system, was used as a reproductive toxicant. 48 female balb/c mice (6–8 weeks) (23–25 g) were randomly divided into eight groups (Grp.1–Grp.8; n = 6) and treated with either nicotine or/and annatto δ-TCT/soy α-TOC for seven consecutive days. On Day 8, the females were superovulated and mated before euthanization for embryo collection (46 h post-coitum). Fifty 2-cell embryos from each group were used in gene expression analysis using Affymetrix QuantiGene Plex2.0 assay. Findings indicated that nicotine (Grp.2) significantly decreased (p < 0.05) the number of produced 2-cell embryos compared to the control (Grp.1). Intervention with mixed annatto δ-TCT (Grp.3) and pure annatto δ-TCT (Grp.4) significantly increased the number of produced 2-cell embryos by 127% and 79%, respectively compared to Grp.2, but these were lower than Grp.1. Concurrent treatment with soy α-TOC (Grp.5) decreased embryo production by 7%. Supplementations with δ-TCT and α-TOC alone (Grp.6-Grp.8) significantly increased (p < 0.05) the number of produced 2-cell embryos by 50%, 36%, and 41%, respectively, compared to control (Grp.1). These results were found to be associated with alterations in the PI3K/Akt-Cyclin D1 genes expressions, indicating the inhibitory effects of annatto δ-TCT and soy α-TOC against nicotinic embryonic damage. To our knowledge, this is the first attempt in studying the benefits of annatto δ-TCT on murine preimplantation 2-cell embryos. © 2019 by the authors. Licensee MDPI, Basel, Switzerland. MDPI AG 2218273X English Article All Open Access; Gold Open Access |
author |
Mutalip S.S.M.; Rajikin M.H.; Rahim S.A.; Khan N.M.N. |
spellingShingle |
Mutalip S.S.M.; Rajikin M.H.; Rahim S.A.; Khan N.M.N. Annatto (Bixa orellana) δ-TCT supplementation protection against embryonic malformations through alterations in PI3K/akt-cyclin D1 pathway |
author_facet |
Mutalip S.S.M.; Rajikin M.H.; Rahim S.A.; Khan N.M.N. |
author_sort |
Mutalip S.S.M.; Rajikin M.H.; Rahim S.A.; Khan N.M.N. |
title |
Annatto (Bixa orellana) δ-TCT supplementation protection against embryonic malformations through alterations in PI3K/akt-cyclin D1 pathway |
title_short |
Annatto (Bixa orellana) δ-TCT supplementation protection against embryonic malformations through alterations in PI3K/akt-cyclin D1 pathway |
title_full |
Annatto (Bixa orellana) δ-TCT supplementation protection against embryonic malformations through alterations in PI3K/akt-cyclin D1 pathway |
title_fullStr |
Annatto (Bixa orellana) δ-TCT supplementation protection against embryonic malformations through alterations in PI3K/akt-cyclin D1 pathway |
title_full_unstemmed |
Annatto (Bixa orellana) δ-TCT supplementation protection against embryonic malformations through alterations in PI3K/akt-cyclin D1 pathway |
title_sort |
Annatto (Bixa orellana) δ-TCT supplementation protection against embryonic malformations through alterations in PI3K/akt-cyclin D1 pathway |
publishDate |
2019 |
container_title |
Biomolecules |
container_volume |
9 |
container_issue |
1 |
doi_str_mv |
10.3390/biom9010019 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85059912784&doi=10.3390%2fbiom9010019&partnerID=40&md5=8d6f8f1938a40a6aab1e17e84362d5db |
description |
Protective action by annatto-derived delta-tocotrienol (δ-TCT) and soy-derived alpha-tocopherol (α-TOC) through the regulation of the PI3K/Akt-cyclin D1 pathway against nicotine-induced DNA damage is the focus of the present study. Nicotine, which has been widely reported to have numerous adverse effects on the reproductive system, was used as a reproductive toxicant. 48 female balb/c mice (6–8 weeks) (23–25 g) were randomly divided into eight groups (Grp.1–Grp.8; n = 6) and treated with either nicotine or/and annatto δ-TCT/soy α-TOC for seven consecutive days. On Day 8, the females were superovulated and mated before euthanization for embryo collection (46 h post-coitum). Fifty 2-cell embryos from each group were used in gene expression analysis using Affymetrix QuantiGene Plex2.0 assay. Findings indicated that nicotine (Grp.2) significantly decreased (p < 0.05) the number of produced 2-cell embryos compared to the control (Grp.1). Intervention with mixed annatto δ-TCT (Grp.3) and pure annatto δ-TCT (Grp.4) significantly increased the number of produced 2-cell embryos by 127% and 79%, respectively compared to Grp.2, but these were lower than Grp.1. Concurrent treatment with soy α-TOC (Grp.5) decreased embryo production by 7%. Supplementations with δ-TCT and α-TOC alone (Grp.6-Grp.8) significantly increased (p < 0.05) the number of produced 2-cell embryos by 50%, 36%, and 41%, respectively, compared to control (Grp.1). These results were found to be associated with alterations in the PI3K/Akt-Cyclin D1 genes expressions, indicating the inhibitory effects of annatto δ-TCT and soy α-TOC against nicotinic embryonic damage. To our knowledge, this is the first attempt in studying the benefits of annatto δ-TCT on murine preimplantation 2-cell embryos. © 2019 by the authors. Licensee MDPI, Basel, Switzerland. |
publisher |
MDPI AG |
issn |
2218273X |
language |
English |
format |
Article |
accesstype |
All Open Access; Gold Open Access |
record_format |
scopus |
collection |
Scopus |
_version_ |
1814778508166037504 |