HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Peptide Transporter 1

A proton-coupled symporter that transports OLIGOPEPTIDES and DIPEPTIDES. It localizes to the brush-border membrane of the INTESTINAL EPITHELIUM and plays a critical role in the assimilation of dietary proteins.
Also Known As:
Hydrogen-Peptide Cotransporter PepT1; Intestinal H+-Peptide Cotransporter; PepT1 Protein; Pept-1 Transporter; SLC15A1 Protein; Solute Carrier Family 15 Member 1; hPEPT1 (Cotransporter); H+-Peptide Cotransporter, Intestinal; Hydrogen Peptide Cotransporter PepT1; Intestinal H+ Peptide Cotransporter; PepT1, Hydrogen-Peptide Cotransporter; Pept 1 Transporter; Transporter, Pept-1
Networked: 37 relevant articles (2 outcomes, 3 trials/studies)

Relationship Network

Bio-Agent Context: Research Results

Experts

1. Kusuhara, Hiroyuki: 2 articles (01/2022 - 01/2021)
2. Maeda, Kazuya: 2 articles (01/2022 - 01/2021)
3. Michiba, Kazuyoshi: 2 articles (01/2022 - 01/2021)
4. Oda, Tatsuya: 2 articles (01/2022 - 01/2021)
5. Shimomura, Osamu: 2 articles (01/2022 - 01/2021)
6. Hyodo, Ichinosuke: 2 articles (07/2014 - 03/2014)
7. Indo, Hiroko P: 2 articles (07/2014 - 03/2014)
8. Ito, Hiromu: 2 articles (07/2014 - 03/2014)
9. Majima, Hideyuki J: 2 articles (07/2014 - 03/2014)
10. Matsui, Hirofumi: 2 articles (07/2014 - 03/2014)

Related Diseases

1. Sepsis (Septicemia)
02/01/2017 - "We tested whether ghrelin administration affects peptide transporter 1 (PepT1) activity in the intestinal epithelium of rats with sepsis. "
11/01/2022 - "Compared with the sepsis group, the abdominal situation in the sepsis+Ghrelin group was improved, the injury of intestinal epithelial cells was alleviated, the serum and small intestinal TNF-α and IL-1β were significantly decreased [serum TNF-α (ng/L): 253.27±23.32 vs. 287.90±19.48, small intestinal TNF-α (ng/L): 95.27±11.47 vs. 153.89±18.15, serum IL-1β (ng/L): 39.16±4.47 vs. 54.26±7.27, small intestinal IL-1β (ng/L): 28.47±4.13 vs. 42.26±2.59, all P < 0.05], and the expressions of PepT1 mRNA and protein in the small intestinal epithelium were significantly increased [PepT1 mRNA (2-ΔΔCt): 0.66±0.05 vs. 0.53±0.06, PepT1 protein (PepT1/GAPDH): 0.80±0.04 vs. 0.60±0.05, both P < 0.05]. "
11/01/2022 - "Compared with the sepsis+Ghrelin group, after vagotomy in the sepsis+vagotomy+Ghrelin group, the effect of Ghrelin on reducing the release of inflammatory factors in sepsis rats was significantly reduced [serum TNF-α (ng/L): 276.58±19.88 vs. 253.27±23.32, small intestinal TNF-α (ng/L): 144.28±12.99 vs. 95.27±11.47, serum IL-1β (ng/L): 48.15±3.21 vs. 39.16±4.47, small intestinal IL-1β (ng/L): 38.75±4.49 vs. 28.47±4.13, all P < 0.05], the up-regulated effect on the expression of PepT1 in small intestinal epithelium was lost [PepT1 mRNA (2-ΔΔCt): 0.58±0.03 vs. 0.66±0.05, PepT1 protein (PepT1/GAPDH): 0.70±0.02 vs. 0.80±0.04, both P < 0.05], and the injury of small intestinal epithelial cells was worse. "
2. Necrosis
3. Neoplasms (Cancer)
4. Breast Neoplasms (Breast Cancer)
01/01/2021 - "In the ileum, apical transporters such as P-gp, peptide transporter 1, breast cancer resistance protein, MRP2, and ASBT were strongly expressed, and the expression levels of P-gp and ASBT in the ileum were higher than those in other regions. "
12/01/2017 - "This study aimed to investigate quantitatively the effect of 5-FU-induced intestinal damage on the expression of intestinal transporters: P-glycoprotein (P-gp), breast cancer resistance protein (BCRP) and peptide transporter 1 (PEPT1) in rats. "
05/06/2013 - "Transcellular transport and cellular/vesicular uptake assays were performed using Caco-2 cells and/or human intestinal efflux (P-glycoprotein [P-gp], breast cancer resistance protein [BCRP], and multidrug resistance associated protein 2 [MRP2]) and influx (peptide transporter 1 [PEPT1], OATP1A2, and OATP2B1) transporter-expressing cells, vesicles, or Xenopus laevis oocytes. "
01/01/2013 - "The increased activities of the most important intestinal efflux (P-glycoprotein - Pgp, Multidrug Resistance Associated Protein 2 - MRP-2, Breast Cancer Resistance Protein - BCRP) and uptake (MonoCarboxylate Transporter 1 - MCT1, Organic Anion Transporting Polypeptide - OATP, Peptide transporter 1 - PepT1) transporters were caused by changes in electrophysiological membrane properties and by allosteric modifications. "
09/10/2020 - "Experiments using known substrates of peptide transporter 1 (PEPT1), organic anion transporting polypeptide (OATP2B1), organic cation transporter 1 (OCT1), P-glycoprotein (P-gp), breast cancer resistance protein (BCRP), multi drug resistance-associated protein 2 and 3 (MRP2 and MRP3), in the absence and presence of potent inhibitors, showed that there was a statistically significant change in apparent intestinal permeability Papp,pig (cm/s) in the presence of the corresponding inhibitor. "
5. Pancreatic Neoplasms (Pancreatic Cancer)

Related Drugs and Biologics

1. Proteins (Proteins, Gene)
2. Messenger RNA (mRNA)
3. Fatty Acid-Binding Proteins
4. Chemokines
5. Interleukin-8 (Interleukin 8)
6. Cytokines
7. Interleukin-6 (Interleukin 6)
8. Zinc Oxide
9. Member 1 Subfamily B ATP Binding Cassette Transporter
10. Heme (Haem)

Related Therapies and Procedures

1. Vagotomy