Analgesics promote welfare and sustain tumour growth in orthotopic 4T1 and B16 mouse cancer models

被引:30
|
作者
Lofgren, Jennifer [1 ]
Miller, Amy L. [2 ]
Lee, Claudia Chui Shan [3 ]
Bradshaw, Carla [3 ]
Flecknell, Paul [3 ]
Roughan, Johnny [3 ]
机构
[1] Univ Michigan, Med Sch, Unit Lab Anim Med, Ann Arbor, MI 48109 USA
[2] Newcastle Univ, Sch Agr Food & Rural Dev, Newcastle Upon Tyne, Tyne & Wear, England
[3] Newcastle Univ, Pain & Anim Welf Sci Grp, Inst Neurosci, Comparat Biol Ctr, Newcastle Upon Tyne, Tyne & Wear, England
基金
英国国家替代、减少和改良动物研究中心;
关键词
mouse; buprenorphine; NSAID; meloxicam; analgesia; cancer; refinement; BREAST-CANCER; POSTOPERATIVE PAIN; RESTRAINT STRESS; RATS; SURGERY; BUPRENORPHINE; MICE; INHIBITION; RECURRENCE; GUIDELINES;
D O I
10.1177/0023677217739934
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Murine orthotopic cancer models often require surgery, potentially causing pain or distress. However, analgesics are often withheld because they may alter tumour development. Two orthotopically implanted cancers were investigated in mice pre-treated with meloxicam (10 mg/kg), buprenorphine (0.2 mg/kg) or saline (1 ml/kg). Tumours were imaged and welfare was assessed using body weight, behaviour and nociceptive responses. In study 1, BALB/c mice were inoculated with 4T1 mammary carcinoma or saline during surgery or anaesthesia. As pre-treatment with a single buprenorphine dose appeared beneficial to cancer growth consistency, a second cohort of mice additionally received saline or buprenorphine at 12 and 24 h. Surgery resulted in increased mammary tumour growth and lung metastases. These unwanted effects were lessened by buprenorphine pre-treatment, especially when given repeatedly. Mammary tumour-bearing mice became less active and nociceptive thresholds declined over time, indicating some discomfort as tumours grew. In study 2, C57BL/6 mice received B16 melanoma. This non-surgical model was used to determine whether meloxicam or buprenorphine affected cancer seeding of the lungs. While meloxicam reduced 616 lung seeding, buprenorphine did not. Mechanical thresholds decreased as cancer developed in mice bearing melanoma, but the magnitude of this was insufficient to conclude that there were any significant welfare concerns. This study highlights the scientific value in utilising non-surgical models, where possible. When surgery must be performed at the time of tumour inoculation, the effects of this should be controlled with appropriate analgesics to enhance the value and possibly translation of the research.
引用
收藏
页码:351 / 364
页数:14
相关论文
共 50 条
  • [1] Passage Number of 4T1 Cells Influences the Development of Tumour and the Progression of Metastasis in 4T1 Orthotopic Mice
    Rajaratinam, Harishini
    Rasudin, Nur Syahmina
    Safuan, Sabreena
    Abdullah, Nurul Asma
    Mokhtar, Noor Fatmawati
    Mohd Fuad, Wan Ezumi
    MALAYSIAN JOURNAL OF MEDICAL SCIENCES, 2022, 29 (03): : 30 - 42
  • [2] Escherichia coli Nissle 1917 Targets and Restrains Mouse B16 Melanoma and 4T1 Breast Tumors through Expression of Azurin Protein
    Zhang, Yunlei
    Zhang, Youming
    Xia, Liqiu
    Zhang, Xiangli
    Ding, Xuezhi
    Yan, Fu
    Wu, Feng
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2012, 78 (21) : 7603 - 7610
  • [3] Macrophages promote tumour growth and liver metastasis in an orthotopic syngeneic mouse model of colon cancer
    J. Kruse
    W. von Bernstorff
    K. Evert
    N. Albers
    S. Hadlich
    S. Hagemann
    C. Günther
    N. van Rooijen
    C.-D. Heidecke
    L. I. Partecke
    International Journal of Colorectal Disease, 2013, 28 : 1337 - 1349
  • [4] Macrophages promote tumour growth and liver metastasis in an orthotopic syngeneic mouse model of colon cancer
    Kruse, J.
    von Bernstorff, W.
    Evert, K.
    Albers, N.
    Hadlich, S.
    Hagemann, S.
    Guenther, C.
    van Rooijen, N.
    Heidecke, C. -D.
    Partecke, L. I.
    INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 2013, 28 (10) : 1337 - 1349
  • [5] Pulsed-Focused Ultrasound Slows B16 Melanoma and 4T1 Breast Tumor Growth through Differential Tumor Microenvironmental Changes
    Cohen, Gadi
    Chandran, Parwathy
    Lorsung, Rebecca M.
    Aydin, Omer
    Tomlinson, Lauren E.
    Rosenblatt, Robert B.
    Burks, Scott R.
    Frank, Joseph A.
    CANCERS, 2021, 13 (07)
  • [6] Nanopulse Stimulation (NPS) Induces Tumor Ablation and Immunity in Orthotopic 4T1 Mouse Breast Cancer: A Review
    Beebe, Stephen J.
    Lassiter, Brittany P.
    Guo, Siqi
    CANCERS, 2018, 10 (04)
  • [7] Luciferase Expression Allows Bioluminescence Imaging But Imposes Limitations on the Orthotopic Mouse (4T1) Model of Breast Cancer
    V. P. Baklaushev
    A. Kilpeläinen
    S. Petkov
    M. A. Abakumov
    N. F. Grinenko
    G. M. Yusubalieva
    A. A. Latanova
    I. L. Gubskiy
    F. G. Zabozlaev
    E. S. Starodubova
    T. O. Abakumova
    M. G. Isaguliants
    V. P. Chekhonin
    Scientific Reports, 7
  • [8] Luciferase Expression Allows Bioluminescence Imaging But Imposes Limitations on the Orthotopic Mouse (4T1) Model of Breast Cancer
    Baklaushev, V. P.
    Kilpelainen, A.
    Petkov, S.
    Abakumov, M. A.
    Grinenko, N. F.
    Yusubalieva, G. M.
    Latanova, A. A.
    Gubskiy, I. L.
    Zabozlaev, F. G.
    Starodubova, E. S.
    Abakumova, T. O.
    Isaguliants, M. G.
    Chekhonin, V. P.
    SCIENTIFIC REPORTS, 2017, 7
  • [9] Anticancer Activity of Saponins from Allium chinense against the B16 Melanoma and 4T1 Breast Carcinoma Cell
    Yu, Zhihui
    Zhang, Tong
    Zhou, Fengjuan
    Xiao, Xiuqing
    Ding, Xuezhi
    He, Hao
    Rang, Jie
    Quan, Meifang
    Wang, Ting
    Zuo, Mingxing
    Xia, Liqiu
    EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2015, 2015
  • [10] DIFFERENTIAL EFFECTS OF NITRIC OXIDE DEFICIENCY ON PRIMARY TUMOUR GROWTH, PULMONARY METASTASIS AND PROSTACYCLIN/THROMBOXANE A2 BALANCE IN ORTHOTOPIC AND INTRAVENOUS MURINE MODELS OF 4T1 BREAST CANCER
    Kij, A.
    Kus, K.
    Smeda, M.
    Zakrzewska, A.
    Proniewski, B.
    Matyjaszczyk, K.
    Jasztal, A.
    Stojak, M.
    Walczak, M.
    Chlopicki, S.
    JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 2018, 69 (06): : 911 - 919