Rating
Oops! The Black Lotus Can’t Be a Female Supporting Character Average 5 / 5 out of 1
Rank
98th, it has 435 monthly views
Alternative
????????????
Type
Chinese Web Novel
Summary
Xiao Yanfei, after transmigrating into a book, believed that her identity was not simple, as evidenced by the following:
1. She was a concubine’s daughter in the Marquis’s household, but her appearance was unparalleled.
2. Her legitimate sister was the female lead, currently engaged to the Crown Prince.
3. She maintained a good friendship with the Second Prince, a villain character with an abundance of buffs.
According to the laws of transmigration, she was undoubtedly an extremely important… villainous character.
And she would sacrifice her intelligence, dignity, and even her life for the breathtaking love of the male and female leads in critical moments.
At first, Xiao Yanfei just wanted to keep a low profile, avoiding “sacrificing” her life and achieving the worst possible ending.
Later, she discovered that the original host had been switched at birth with the female lead, and she had even considered the villain as her birth mother. Under the “earnest guidance” of her stepmother, she willingly endured any hardship for the sake of the female lead.
Meanwhile, the reborn female lead took over the original host’s identity, trampling on her tragic past and enacting a “breathtaking love” with the Crown Prince!
Xiao Yanfei: …Tired.
She rolled up her sleeves, sharpened her blade, and was determined to tear apart this melodramatic plot and set things right!
The Second Prince, with a stack of villainous buffs: Do you need help?
Xiao Yanfei: Yes.
*
Gu Feichi, the eldest son of Duke Weiguo, was unruly and unconventional. He conquered the western barbarians and pacified the northern tribes. His military prowess was unmatched, and he opened up vast territories.
With half of his face concealed by a mask and a scarlet robe billowing, he extended his hand to her amid thousands of troops and horses: “From now on…”
“Those who follow you will prosper, those who oppose you will perish!”
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“In phrases of the protection profiles of ?-MSH and its tripeptides, only a few data are at present available as a result of lack of toxicity research. However, the super-potent analog of ?-MSH, [Nle4-D-Phe7]-MSH, when administrated intravenously at doses of as much as 0.6 mg/kg, results in occasional gastrointestinal upset and facial flushing with out major detrimental results.
An unhealthy intestine can exhibit symptoms such as nausea, vomiting, belly ache, distention, constipation, diarrhea, or diseases similar to ulcers, Irritable Bowel Syndrome (IBS), Crohn’s Illness, and Ulcerative Colitis. Nevertheless, “if we are to achieve the
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When you mix KPV peptide with clever programming, trustworthy sleep, protein self-discipline, and actual load management, the result is simple. When there is a larger delicate tissue insult, athletes typically pair them. This pairing must be managed by a clinician because systemic instruments deserve professional oversight. KPV effectively manages and reduces irritation throughout administration. Sustained anti-inflammatory results usually require ongoing remedy or adjunctive therapeutic approaches. You can find peptide KPV in topical lotions, oral capsules, and generally in injectable kind (under medical supervision). Oral choices are popular for gut well being, whereas topical options are higher for pores and skin restore.
Thus, KPV mediates its main anti-inflammatory impact through the nuclear transport system and independently of melanocortin receptors. The pharmaceutical growth of KPV as an anti-inflammatory therapy may subsequently depend upon the degree to which it could be focused to specific interactions between importin molecules and their protein cargo. ?-MSH and other melanocortin peptides are potent anti-inflammatory brokers and have been shown to be effective in lots of diseases (30). Here, we demonstrate that the tripeptide KPV, which is the C-terminal sequence of ?-MSH, has an anti-inflammatory effect in vitro and in vivo. We show that the anti-inflammatory effect of KPV just isn’t melanocortin receptor-mediated but PepT1-mediated. Moreover, it was recently demonstrated that KPV does not bind to MC1,three,5R (32) and doesn’t compete with ?-MSH (20), indicating a non-MCR mechanism.
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To further confirm that hPepT1 transports KPV, uptake experiments were performed utilizing [3H]KPV. We present that, in distinction to [14C]Gly-Sar, nanomolar concentrations of [3H]KPV were efficiently transported by hPepT1 (Figure 4B). These results were confirmed by kinetic experiments displaying that hPepT1 had a low Km of ~160 ?M for KPV (Figure 4C). Collectively, these outcomes present that KPV reduces NF-?B and MAPK activation which represent the classical signaling pathways concerned in cytokine secretion by infected IEC. Caco2-BBE and HT29-Cl.19A cells had been grown in DMEM supplemented with 14 mM NaHCO3, 10% FBS, and penicillin/streptomycin (Invitrogen, Grand Island, NY). Jurkat cells have been grown in RPMI 1640 (Invitrogen) supplemented with 10% FBS. I am 21 years or older and understand that the products listed on this web site are for research purposes only.
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