Literature DB >> 26456655

New synthetic peptide with efficacy for heparin reversal and low toxicity and immunogenicity in comparison to protamine sulfate.

Tong Li1, Zhiyun Meng1, Xiaoxia Zhu1, Hui Gan1, Ruolan Gu1, Zhuona Wu1, Jian Li1, Ying Zheng1, Taoyun Liu1, Peng Han1, Su Han1, Guifang Dou2.   

Abstract

Protamine sulfate (PS), the only clinically approved antidote to unfractionated heparin (UFH), is widely used for cardiopulmonary surgery or other extracorporeal circulation situations. However, the applications of PS have accompanied various severe side-effects. In this study, we presented a novel synthesized peptide compound (RRRRR-RRRRR-RRRRR-sulfate, R15S) served as a safer UFH antidote. Comparison studies were conducted between PS and R15S on efficacy and safety, aided by heparin neutralization studies, drug toxicity studies and anaphylactic analysis. Our research demonstrated that R15S contained comparable UFH neutralization activity in vitro and in rats in vivo as to active partial thromboplastin time (APTT) and anti-FXa assays. There was no cytotoxicity for R15S at 60 μg mg(-1) or below and the median lethal dose (LD50) of R15S in mice was 35.4 mg kg(-1), both of which were similar to that of PS. Furthermore, R15S exhibited no immunogenicity while it was obvious in guinea pigs immunized with PS. The level of cross-reactivity to anti-PS antibodies of R15S was about 30%. Both of which indicated much safer properties of R15S than PS. In conclusion, we presented a promising candidate R15S for UFH reversal, which is effective in neutralizing UFH and potentially safer in use.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cross-reactivity; Heparin neutralization; Immunogenicity; Protamine; Protamine toxicity

Mesh:

Substances:

Year:  2015        PMID: 26456655     DOI: 10.1016/j.bbrc.2015.10.020

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  4 in total

1.  Assessment of the Neuroprotective Effects of Arginine-Rich Protamine Peptides, Poly-Arginine Peptides (R12-Cyclic, R22) and Arginine-Tryptophan-Containing Peptides Following In Vitro Excitotoxicity and/or Permanent Middle Cerebral Artery Occlusion in Rats.

Authors:  Bruno P Meloni; Diego Milani; Jane L Cross; Vince W Clark; Adam B Edwards; Ryan S Anderton; David J Blacker; Neville W Knuckey
Journal:  Neuromolecular Med       Date:  2017-05-18       Impact factor: 3.843

2.  Dynamic Combinatorial Optimization of In Vitro and In Vivo Heparin Antidotes.

Authors:  Daniel Carbajo; Yolanda Pérez; Marta Guerra-Rebollo; Eva Prats; Jordi Bujons; Ignacio Alfonso
Journal:  J Med Chem       Date:  2022-03-02       Impact factor: 7.446

Review 3.  Modulating microRNAs in cancer: Next-generation therapies.

Authors:  Nahid Arghiani; Khalid Shah
Journal:  Cancer Biol Med       Date:  2021-12-01       Impact factor: 4.248

4.  In vitro and in vivo safety studies indicate that R15, a synthetic polyarginine peptide, could safely reverse the effects of unfractionated heparin.

Authors:  Tong Li; Zhiyun Meng; Xiaoxia Zhu; Hui Gan; Ruolan Gu; Zhuona Wu; Taoyun Liu; Peng Han; Jiarui Gao; Su Han; Guifang Dou
Journal:  FEBS Open Bio       Date:  2021-08-12       Impact factor: 2.693

  4 in total

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