Biodistribution of the cationic host defense peptide LL-37 using SPECT/CT

被引:0
作者
Esposito, Tullio V. F. [1 ,4 ]
Rodriguez-Rodriguez, Cristina [1 ,2 ]
Blackadar, Colin [1 ]
Klodzinska, Sylvia [3 ]
Nielsen, Hanne Morck [3 ]
Saatchi, Katayoun [1 ]
Hafeli, Urs O. [1 ,3 ]
机构
[1] Univ British Columbia, Fac Pharmaceut Sci, Vancouver, BC, Canada
[2] Univ British Columbia, Fac Sci, Dept Phys & Astron, Vancouver, BC, Canada
[3] Univ Copenhagen, Fac Hlth & Med Sci, Dept Pharm, Copenhagen, Denmark
[4] Mem Sloan Kettering Canc Ctr, Dept Radiol, New York, NY 10065 USA
关键词
LL-37; SPECT/CT; Biodistribution; Host defense peptide; Cathelicidin; ANTIMICROBIAL PEPTIDE; VIVO EFFICACY; CATHELICIDIN; PHARMACOKINETICS; BLOOD; CELLS; ATHEROSCLEROSIS; APOPTOSIS; RECEPTOR;
D O I
10.1016/j.ejpb.2024.114398
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Human cathelicidin LL-37, a cationic host defense peptide (CHDP), has several important physiological roles, including antimicrobial activity, immune modulation, and wound healing, and is a being investigated as a therapeutic candidate for several indications. While the effects of endogenously produced LL-37 are well studied, the biodistribution of exogenously administered LL-37 are less known. Here we assess the biodistribution of a gallium-67 labeled variant of LL-37 using nuclear imaging techniques over a 48 h period in healthy mice. When administered as an intravenous bolus just over 20 mu g, the LL-37-based radiotracer was rapidly cleared from the blood, largely by the liver, while an appreciable fraction of the dose temporarily distributed to the lungs. When administered subcutaneously at the same dose level, the radiotracer was absorbed systemically following a twophase kinetic model and was predominately cleared renally. Uptake into sites rich in immune cells, such as the lymph nodes and the spleen, was observed for both routes of administration. Scans of free gallium-67 were also performed as controls. Important preclinical insights into the biodistribution of exogenously administered LL-37 were gained from this study, which can aid in the understanding of this and related cationic host-defense peptides.
引用
收藏
页数:9
相关论文
共 64 条
  • [1] Pharmacokinetics of novel antimicrobial cationic peptides NAB 7061 and NAB 739 in rats following intravenous administration
    Ali, Feda' Emad Atta
    Cao, Guoying
    Poudyal, Anima
    Vaara, Timo
    Nation, Roger L.
    Vaara, Martti
    Li, Jian
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2009, 64 (05) : 1067 - 1070
  • [2] Augmentation of innate host defense by expression of a cathelicidin antimicrobial peptide
    Bals, R
    Weiner, DJ
    Moscioni, AD
    Meegalla, RL
    Wilson, JM
    [J]. INFECTION AND IMMUNITY, 1999, 67 (11) : 6084 - 6089
  • [3] The Human Cathelicidin LL-37 Preferentially Promotes Apoptosis of Infected Airway Epithelium
    Barlow, Peter G.
    Beaumont, Paula E.
    Cosseau, Celine
    Mackellar, Annie
    Wilkinson, Thomas S.
    Hancock, Robert E. W.
    Haslett, Chris
    Govan, John R. W.
    Simpson, A. John
    Davidson, Donald J.
    [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2010, 43 (06) : 692 - 702
  • [4] The human cationic host defense peptide LL-37 mediates contrasting effects on apoptotic pathways in different primary cells of the innate immune system
    Barlow, Peter G.
    Li, Yuexin
    Wilkinson, Thomas S.
    Bowdish, Dawn M. E.
    Lau, Y. Elaine
    Cosseau, Celine
    Haslett, Christopher
    Simpson, A. John
    Hancock, Robert E. W.
    Davidson, Donald J.
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 2006, 80 (03) : 509 - 520
  • [5] Innate defense regulator peptide 1018 protects against perinatal brain injury
    Bolouri, Hayde
    Savman, Karin
    Wang, Wei
    Thomas, Anitha
    Maurer, Norbert
    Dullaghan, Edie
    Fjell, Christopher D.
    Ek, C. Joakim
    Hagberg, Henrik
    Hancock, Robert E. W.
    Brown, Kelly L.
    Mallard, Carina
    [J]. ANNALS OF NEUROLOGY, 2014, 75 (03) : 395 - 410
  • [6] Acyclic Chelate with Ideal Properties for 68Ga PET Imaging Agent Elaboration
    Boros, Eszter
    Ferreira, Cara L.
    Cawthray, Jacqueline F.
    Price, Eric W.
    Patrick, Brian O.
    Wester, Dennis W.
    Adam, Michael J.
    Orvig, Chris
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (44) : 15726 - 15733
  • [7] Pixel-based subsets for rapid multi-pinhole SPECT reconstruction
    Branderhorst, Woutjan
    Vastenhouw, Brendan
    Beekman, Freek J.
    [J]. PHYSICS IN MEDICINE AND BIOLOGY, 2010, 55 (07) : 2023 - 2034
  • [8] In vitro and in vivo efficacy, toxicity, bio-distribution and resistance selection of a novel antibacterial drug candidate
    Brunetti, Jlenia
    Falciani, Chiara
    Roscia, Giulia
    Pollini, Simona
    Bindi, Stefano
    Scali, Silvia
    Arrieta, Unai Cossio
    Gomez-Vallejo, Vanessa
    Quercini, Leila
    Ibba, Elisa
    Prato, Marco
    Rossolini, Gian Maria
    Llop, Jordi
    Bracci, Luisa
    Pini, Alessandro
    [J]. SCIENTIFIC REPORTS, 2016, 6
  • [9] PLGA nanoparticles loaded with host defense peptide LL37 promote wound healing
    Chereddy, Kiran Kumar
    Her, Charles-Henry
    Comune, Michela
    Moia, Claudia
    Lopes, Alessandra
    Porporato, Paolo E.
    Vanacker, Julie
    Lam, Martin C.
    Steinstraesser, Lars
    Sonveaux, Pierre
    Zhu, Huijun
    Ferreira, Lino S.
    Vandermeulen, Gaelle
    Preat, Veronique
    [J]. JOURNAL OF CONTROLLED RELEASE, 2014, 194 : 138 - 147
  • [10] PHYSIOLOGICAL-PARAMETERS IN LABORATORY-ANIMALS AND HUMANS
    DAVIES, B
    MORRIS, T
    [J]. PHARMACEUTICAL RESEARCH, 1993, 10 (07) : 1093 - 1095