Carcinogenicity Chronic (1 year) repeated topical application of SOOLANTRA enhanced simulated solar ultraviolet radiation-induced non-melanoma skin carcinogenesis in albino Skh HR-1 hairless mouse (tumour potency factor in both sexes combined was 1.69; and 1.74 in male mice and 1.51 in female mice; compared with an expected no adverse effect tumour potency factor of 1.00).
Carcinogenicity Chronic (1 year) repeated topical application of SOOLANTRA enhanced simulated solar ultraviolet radiation-induced non-melanoma skin carcinogenesis in albino Skh HR-1 hairless mouse (tumour potency factor in both sexes combined was 1.69; and 1.74 in male mice and 1.51 in female mice; compared with an expected no adverse effect tumour potency factor of 1.00).
イベルメクチンは広範な哺乳類の細胞に対して細胞生存率を著しく下げる毒性がある According to reports, IVM (1–280 μΜ) can significantly inhibit the cell viability of widely spread non-target mammalian cells (Molinari et al., 2009b, 2013). 本研究では人間の培養細胞に対してイベルメクチンがオートファジーを引き起こし細胞死を促すと判明 In the present study, we found that IVM-mediated proliferation inhibition in HeLa cells were markedly reverted by the addition of 3-MA. The result reflects that IVM can promote cell death by inducing autophagy in HeLa cells. イベルメクチンの細胞毒性メカニズムはAMPK/mTOR由来オートファジーおよびDNA酸化ダメージである可能性がある The mechanism of ivermectin’s cytotoxicity might be the AMPK/mTOR mediated autophagy and oxidative DNA damage. https://www.sciencedirect.com/science/article/pii/S0045653520316428?casa_token=grsoFiHgtasAAAAA:Rw1IbmA3vgPKjiGokdnzHyA5Rn0AeNvf7fruBmCUCJ2D2K0bUWw6wI7sTrQo4A8MTAo0n3-J0hZF0620名無しさん＠お腹いっぱい。2022/07/22(金) 13:29:18.74ID:FNCbgtoW>>617 工作員曰く イベルメクチンに対する論文で 「＞＞人間に発がん性があると指摘された物は歴史上一つもねーよw」
イベルメクチンは広範な哺乳類の細胞に対して細胞生存率を著しく下げる毒性がある According to reports, IVM (1–280 μΜ) can significantly inhibit the cell viability of widely spread non-target mammalian cells (Molinari et al., 2009b, 2013). 本研究では人間の培養細胞に対してイベルメクチンがオートファジーを引き起こし細胞死を促すと判明 In the present study, we found that IVM-mediated proliferation inhibition in HeLa cells were markedly reverted by the addition of 3-MA. The result reflects that IVM can promote cell death by inducing autophagy in HeLa cells. イベルメクチンの細胞毒性メカニズムはAMPK/mTOR由来オートファジーおよびDNA酸化ダメージである可能性がある The mechanism of ivermectin’s cytotoxicity might be the AMPK/mTOR mediated autophagy and oxidative DNA damage. https://www.sciencedirect.com/science/article/pii/S0045653520316428?casa_token=grsoFiHgtasAAAAA:Rw1IbmA3vgPKjiGokdnzHyA5Rn0AeNvf7fruBmCUCJ2D2K0bUWw6wI7sTrQo4A8MTAo0n3-J0hZF0625名無しさん＠お腹いっぱい。2022/07/22(金) 13:44:32.69ID:bs3WxA8j>>620 バカメクチンの「抗がん効果」は完全に0 バカメクチン５μMで40%の健康な免疫細胞が死ぬwwwww バカメクチン５μMで40%のがん細胞が死ぬwwwww つまりバカメクチンは無差別に細胞を殺すだけのただの毒で抗がん効果は完全に0wwwwwww
イベルメクチンは広範な哺乳類の細胞に対して細胞生存率を著しく下げる毒性がある According to reports, IVM (1–280 μΜ) can significantly inhibit the cell viability of widely spread non-target mammalian cells (Molinari et al., 2009b, 2013). 本研究では人間の培養細胞に対してイベルメクチンがオートファジーを引き起こし細胞死を促すと判明 In the present study, we found that IVM-mediated proliferation inhibition in HeLa cells were markedly reverted by the addition of 3-MA. The result reflects that IVM can promote cell death by inducing autophagy in HeLa cells. イベルメクチンの細胞毒性メカニズムはAMPK/mTOR由来オートファジーおよびDNA酸化ダメージである可能性がある The mechanism of ivermectin’s cytotoxicity might be the AMPK/mTOR mediated autophagy and oxidative DNA damage. https://www.sciencedirect.com/science/article/pii/S0045653520316428?casa_token=grsoFiHgtasAAAAA:Rw1IbmA3vgPKjiGokdnzHyA5Rn0AeNvf7fruBmCUCJ2D2K0bUWw6wI7sTrQo4A8MTAo0n3-J0hZF0630名無しさん＠お腹いっぱい。2022/07/22(金) 14:44:07.45ID:bs3WxA8j イベルメクチンクリームの発がん性は添付文書にも書いてあるからなあwwww
Carcinogenicity Chronic (1 year) repeated topical application of SOOLANTRA enhanced simulated solar ultraviolet radiation-induced non-melanoma skin carcinogenesis in albino Skh HR-1 hairless mouse (tumour potency factor in both sexes combined was 1.69; and 1.74 in male mice and 1.51 in female mice; compared with an expected no adverse effect tumour potency factor of 1.00).
Our current observation allows us to communicate for the first time the in vitro evaluation of DNA damage produced by these antiparasiticides: a brief 80 min pulse-treatment of 5.0–50.0 μg/ml of IVM or 25.0 and 50.0 μg/ml of ivomec®, resulted in a manifest level of single DNA-strand break induction. This findings are in concordance with previous observations showing a genotoxic effect exerted by the abamectin, the most active form of the avermectin (avermectin B1a), able to induce single strand DNA breaks in rat hepatocytes from rats treated in vivo [27].
IVM reduced testicular volume, tubular diameter and germinal epithelium height. Spermatogenesis interruption, such as degeneration morphology of the germ cells
This findings are in concordance with previous observations showing a genotoxic effect exerted by the abamectin, the most active form of the avermectin (avermectin B1a), able to induce single strand DNA breaks in rat hepatocytes from rats treated in vivo [27]. 0636名無しさん＠お腹いっぱい。2022/07/22(金) 15:01:37.19ID:bs3WxA8j 発がん性の人体実験は許されてないから動物実験と人間の細胞での実験しかどんな物質でも不可能 つまり動物実験と人間の細胞で発がん性が確認されたらそれは100%黒 0637名無しさん＠お腹いっぱい。2022/07/22(金) 15:13:23.21ID:FNCbgtoW 英語の読めないアホ工作員(東京都) ↓ 600 名無しのアビガン(東京都) (ﾜｯﾁｮｲW 7658-+tgD) 2022/07/22(金) 12:22:36.67 ID:Wrl7pox90 イベルメクチンクリームの発がん性は添付文書にも書いてあるからなあwwww
Carcinogenicity Chronic (1 year) repeated topical application of SOOLANTRA enhanced simulated solar ultraviolet radiation-induced non-melanoma skin carcinogenesis in albino Skh HR-1 hairless mouse (tumour potency factor in both sexes combined was 1.69; and 1.74 in male mice and 1.51 in female mice; compared with an expected no adverse effect tumour potency factor of 1.00).
イベルメクチンは広範な哺乳類の細胞に対して細胞生存率を著しく下げる毒性がある According to reports, IVM (1–280 μΜ) can significantly inhibit the cell viability of widely spread non-target mammalian cells (Molinari et al., 2009b, 2013). 本研究では人間の培養細胞に対してイベルメクチンがオートファジーを引き起こし細胞死を促すと判明 In the present study, we found that IVM-mediated proliferation inhibition in HeLa cells were markedly reverted by the addition of 3-MA. The result reflects that IVM can promote cell death by inducing autophagy in HeLa cells. イベルメクチンの細胞毒性メカニズムはAMPK/mTOR由来オートファジーおよびDNA酸化ダメージである可能性がある The mechanism of ivermectin’s cytotoxicity might be the AMPK/mTOR mediated autophagy and oxidative DNA damage. https://www.sciencedirect.com/science/article/pii/S0045653520316428?casa_token=grsoFiHgtasAAAAA:Rw1IbmA3vgPKjiGokdnzHyA5Rn0AeNvf7fruBmCUCJ2D2K0bUWw6wI7sTrQo4A8MTAo0n3-J0hZF0640名無しさん＠お腹いっぱい。2022/07/22(金) 15:23:28.58ID:7UQ/2jgI まあこういうの読めるなら北里大学なんてそもそも受けないというねwww
This findings are in concordance with previous observations showing a genotoxic effect exerted by the abamectin, the most active form of the avermectin (avermectin B1a), able to induce single strand DNA breaks in rat hepatocytes from rats treated in vivo [27]. 0641名無しさん＠お腹いっぱい。2022/07/22(金) 15:32:31.01ID:FNCbgtoW 工作員ID:bs3WxA8j 「イベルメクチンクリームに発がん性！ 添付文書に書いてたぞ！！」
イベルメクチンは広範な哺乳類の細胞に対して細胞生存率を著しく下げる毒性がある According to reports, IVM (1–280 μΜ) can significantly inhibit the cell viability of widely spread non-target mammalian cells (Molinari et al., 2009b, 2013). 本研究では人間の培養細胞に対してイベルメクチンがオートファジーを引き起こし細胞死を促すと判明 In the present study, we found that IVM-mediated proliferation inhibition in HeLa cells were markedly reverted by the addition of 3-MA. The result reflects that IVM can promote cell death by inducing autophagy in HeLa cells. イベルメクチンの細胞毒性メカニズムはAMPK/mTOR由来オートファジーおよびDNA酸化ダメージである可能性がある The mechanism of ivermectin’s cytotoxicity might be the AMPK/mTOR mediated autophagy and oxidative DNA damage. https://www.sciencedirect.com/science/article/pii/S0045653520316428?casa_token=grsoFiHgtasAAAAA:Rw1IbmA3vgPKjiGokdnzHyA5Rn0AeNvf7fruBmCUCJ2D2K0bUWw6wI7sTrQo4A8MTAo0n3-J0hZF0643名無しさん＠お腹いっぱい。2022/07/22(金) 15:46:14.93ID:bs3WxA8j そもそもアバメクチンがDNA破壊することは常識なのにwww
まあこういうの読めるなら北里大学なんてそもそも受けないというねwww
This findings are in concordance with previous observations showing a genotoxic effect exerted by the abamectin, the most active form of the avermectin (avermectin B1a), able to induce single strand DNA breaks in rat hepatocytes from rats treated in vivo [27].
