Novel Small Molecule, UTS-1401, as a Radioprotector for Total-Body Irradiation

被引:0
作者
Valeriote, Frederick A. [1 ]
Brown, Stephen L. [2 ]
Media, Joseph [1 ]
Li, Pin [3 ]
Maheshwari, Mani [1 ]
Shaw, Jiajiu [4 ]
机构
[1] Henry Ford Hlth, Dept Internal Med, Detroit, MI 48202 USA
[2] Henry Ford Hlth, Dept Radiat Oncol, Detroit, MI 48202 USA
[3] Henry Ford Hlth, Dept Publ Hlth Sci, Detroit, MI 48202 USA
[4] 21st Century Therapeut Inc, Detroit, MI 48202 USA
基金
美国国家卫生研究院;
关键词
COLONY-STIMULATING FACTOR; ACUTE-RADIATION-SYNDROME; AMIFOSTINE; THERAPY; MOUSE; RECOVERY; INJECTION; TOXICITY; TISSUES; GROWTH;
D O I
10.1667/RADE-22-00030.1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We report on a new radioprotector, UTS-1401, a small molecule that was synthesized (by one of us, JS) and evaluated here for its radioprotective effect against total-body irradiation (TBI). Female and male NIH Swiss mice were subjected to TBI at doses of 6.5, 7.5 and 8.5 Gy either with or without a 24 h pretreatment of UTS-1401 given ip and observed for 30 days. Survival rates were significantly increased when mice were treated with UTS-1401 compared to those not treated. The radioprotective effect of UTS-1401 was drug-dose dependent for male mice exposed to 8.5 Gy TBI with 150 mg/kg of UTS-1401 as the optimal dose. The radioprotective effect of UTS-1401 on female mice exposed to 8.5 Gy TBI was observed at 50, 100, and 150 mg/kg, with no dose response relationship noted. Female mice were more radioresistant than male mice with LD50/30 values of 7.8 Gy vs. 6.8 Gy, respectively. Weight changes after UTS-1401 alone showed a significant body weight increase at 150 mg/kg. Both the ip and iv route for UTS-1401 were similarly effective for male mice exposed to 8 Gy TBI. Further analysis using an endogenous spleen colony assay demonstrated that pretreatment of UTS-1401 for up to 72h prior to TBI protected both spleen weight and hematopoietic stem cells with a treated/untreated ratio between 2.0 and 3.2 for the latter for times between 0.5 h and 72 h. A separate in vivo study showed that pretreatment of UTS-1401 protected bone marrow CFU-GM for mice exposed to TBI. In summary, UTS-1401 is a promising small-molecule radioprotective agent as demonstrated by whole animal, hematopoietic stem cell and bone marrow myeloid progenitor cell survival. (C) 2024 by Radiation Research Society
引用
收藏
页码:16 / 25
页数:10
相关论文
共 38 条
  • [1] Chemical radioprotection: A critical review of amifostine as a cytoprotector in radiotherapy
    Andreassen, CN
    Gran, C
    Lindegaard, JC
    [J]. SEMINARS IN RADIATION ONCOLOGY, 2003, 13 (01) : 62 - 72
  • [2] Comparison of autologous cell therapy and granulocyte-colony stimulating factor (G-CSF) injection vs. G-CSF injection alone for the treatment of acute radiation syndrome in a non-human primate model
    Bertho, JM
    Frick, J
    Prat, M
    Demarquay, C
    Dudoignon, N
    Trompier, F
    Gorin, NC
    Thierry, D
    Gourmelon, P
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2005, 63 (03): : 911 - 920
  • [3] CHARACTERIZATION OF A 137Cs IRRADIATOR FROM A NEW PERSPECTIVE WITH MODERN DOSIMETRIC TOOLS
    Brady, Samuel L.
    Toncheva, Greta
    Dewhirst, Mark W.
    Yoshizumi, Terry T.
    [J]. HEALTH PHYSICS, 2009, 97 (03): : 195 - 205
  • [4] An agonist of toll-like receptor 5 has radioprotective activity in mouse and primate models
    Burdelya, Lyudmila G.
    Krivokrysenko, Vadim I.
    Tallant, Thomas C.
    Strom, Evguenia
    Gleiberman, Anatoly S.
    Gupta, Damodar
    Kurnasov, Oleg V.
    Fort, Farrel L.
    Osterman, Andrei L.
    DiDonato, Joseph A.
    Feinstein, Elena
    Gudkov, Andrei V.
    [J]. SCIENCE, 2008, 320 (5873) : 226 - 230
  • [5] Phosphoproteome and transcription factor activity profiling identify actions of the anti-inflammatory agent UTL-5g in LPS stimulated RAW 264.7 cells including disrupting actin remodeling and STAT-3 activation
    Carruthers, Nicholas J.
    Stemmer, Paul M.
    Chen, Ben
    Valeriote, Frederick
    Gao, Xiaohua
    Guatam, Subhash C.
    Shaw, Jiajiu
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2017, 811 : 66 - 73
  • [6] AMIFOSTINE INDUCES ANTIOXIDANT ENZYMATIC ACTIVITIES IN NORMAL TISSUES AND A TRANSPLANTABLE TUMOR THAT CAN AFFECT RADIATION RESPONSE
    Grdina, David J.
    Murley, Jeffrey S.
    Kataoka, Yasushi
    Baker, Kenneth L.
    Kunnavakkam, Rangesh
    Coleman, Mitchell C.
    Spitz, Douglas R.
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2009, 73 (03): : 886 - 896
  • [7] HIRSCHELSCHOLZ S, 1988, MINER ELECTROL METAB, V14, P114
  • [8] Foundation review: Trends in the development of radioprotective agents
    Hosseinimehr, Seyed Jalal
    [J]. DRUG DISCOVERY TODAY, 2007, 12 (19-20) : 794 - 805
  • [9] Radioprotective agents for radiation therapy: future trends
    Johnke, Roberta M.
    Sattler, Jennifer A.
    Allison, Ron R.
    [J]. FUTURE ONCOLOGY, 2014, 10 (15) : 2345 - 2357
  • [10] Mitigation of hematologic radiation toxicity in mice through pharmacological quiescence induced by CDK4/6 inhibition
    Johnson, Soren M.
    Torrice, Chad D.
    Bell, Jessica F.
    Monahan, Kimberly B.
    Jiang, Qi
    Wang, Yong
    Ramsey, Matthew R.
    Jin, Jian
    Wong, Kwok-Kin
    Su, Lishan
    Zhou, Daohong
    Sharpless, Norman E.
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2010, 120 (07) : 2528 - 2536