U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination
    • Showing Current items.

    Nmbr neuromedin B receptor [ Mus musculus (house mouse) ]

    Gene ID: 18101, updated on 12-May-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    Disruption of neuromedin B receptor improves mitochondrial oxidative phosphorylation capacity in gastrocnemius muscle of female mice.

    Disruption of neuromedin B receptor improves mitochondrial oxidative phosphorylation capacity in gastrocnemius muscle of female mice.
    Bento-Bernardes T, Rossetti CL, Borba Vieira de Andrade C, Lopes de Souza L, Wilieman Cabral M, Silva Monteiro de Paula G, Woyames J, Jesus Oliveira K, Seixas da-Silva W, Cabanelas Pazos-Moura C.

    05/14/2022
    Data show genetically disruption of NB-R in mice ASC or pharmacological antagonism of NB-R in 3T3-L1 cells impairs adipogenesis.

    Neuromedin B receptor disruption impairs adipogenesis in mice and 3T3-L1 cells.
    de Paula GSM, Wilieman M, Silva KR, Baptista LS, Boudina S, de Souza LL, Bento-Bernardes T, Asensi KD, Goldenberg RCDS, Pazos-Moura CC., Free PMC Article

    07/18/2020
    NMB-treated mice were less susceptible to virus challenge, as evidenced by increased survival, increased body weight, and decreased viral NP expression compared with the control animals. As expected, opposing effects were observed in the NMBR antagonist-treated cells and mice, which further confirmed the effects of NMB.

    Role of neuromedin B and its receptor in the innate immune responses against influenza A virus infection in vitro and in vivo.
    Yang G, Huang H, Tang M, Cai Z, Huang C, Qi B, Chen JL., Free PMC Article

    02/8/2020
    Neuromedin B expression identifies retrotrapezoid nucleus neurons in the mouse.

    Neuromedin B Expression Defines the Mouse Retrotrapezoid Nucleus.
    Shi Y, Stornetta RL, Stornetta DS, Onengut-Gumuscu S, Farber EA, Turner SD, Guyenet PG, Bayliss DA., Free PMC Article

    12/9/2017
    NMB or NMBR silencing inhibited M-CSF/c-Fms-mediated downstream signaling pathways like activation of ERK and Akt and induction of D-type cyclins, cyclin D1 and D2.

    Neuromedin B and its receptor silencing suppresses osteoclast generation by modulating precursor proliferation via M-CSF/c-Fms/D-type cyclins.
    Yeo CE, Kang WY, Seong SJ, Cho S, Lee HW, Yoon YR, Kim HJ.

    10/21/2017
    mice with deletion of NB receptor have lower insulinemia, especially in response to oral glucose, and females also exhibited a better glucose tolerance, suggesting the involvement of neuromedin b and its receptor in regulation of insulin secretion induced by incretins, and also, in insulin sensitivity.

    Mice with Deletion of Neuromedin B Receptor Exhibit Decreased Oral Glucose-Stimulated Insulin Release.
    Paula GS, Souza LL, Bressane NO, Maravalhas R, Wilieman M, Bento-Bernardes T, Silva KR, Mendonca LS, Oliveira KJ, Pazos-Moura CC.

    03/18/2017
    ablating NMB receptor-expressing neurons eliminated basal and hypoxia-induced sighing, but left breathing otherwise intact initially

    The peptidergic control circuit for sighing.
    Li P, Janczewski WA, Yackle K, Kam K, Pagliardini S, Krasnow MA, Feldman JL., Free PMC Article

    03/12/2016
    The neuromedin B pathways are importantly involved in secretory pathways of TSH and revealed its participation in the in vivo regulation of gene expression of TSH beta-subunit and pituitary MCT8 and Thrb and hypothalamic TRH and type 2 deiodinase.

    Hypothalamic-pituitary thyroid axis alterations in female mice with deletion of the neuromedin B receptor gene.
    Oliveira KJ, Paula GS, Império GE, Bressane NO, Magalhães CM, Miranda-Alves L, Ortiga-Carvalho TM, Pazos-Moura CC.

    01/2/2016
    Together, we define the respective function of NMBR and GRPR in itch transmission, and reveal an unexpected relationship not only between the two receptors but also between the two populations of interneurons in itch signaling.

    Cross-inhibition of NMBR and GRPR signaling maintains normal histaminergic itch transmission.
    Zhao ZQ, Wan L, Liu XY, Huo FQ, Li H, Barry DM, Krieger S, Kim S, Liu ZC, Xu J, Rogers BE, Li YQ, Chen ZF., Free PMC Article

    01/10/2015
    spinal GRPr and NMBr independently drive itch neurotransmission in mice.

    Physiological function of gastrin-releasing peptide and neuromedin B receptors in regulating itch scratching behavior in the spinal cord of mice.
    Sukhtankar DD, Ko MC., Free PMC Article

    02/8/2014
    Results implicate that NMB is involved in cartilage development, either in an autocrine or paracrine manner.

    Neuromedin B stimulates proliferation of mouse chondrogenic cell line ATDC5.
    Saito H, Ikeda R, Inoue K, Nagata S, Kitamura K, Minamino N, Kangawa K, Miyata A.

    12/29/2012
    The data demonstrated that the neuromedin B-neuromedian B receptor interaction in pregnant myometrial primary cells in vitro predominantly influenced uterine activity through regulation of Il6 expression via the Rela/p65 pathway.

    Neuromedin B and its receptor influence the activity of myometrial primary cells in vitro through regulation of Il6 expression via the Rela/p65 pathway in mice.
    Zhang WS, Fei KL, Wu MT, Wu XH, Liang QH.

    09/22/2012
    These data demonstrate that neuromedin B and its receptor can induce the onset of labor via a RELA/IL6-mediated pathway.

    Neuromedin B and its receptor induce labor onset and are associated with the RELA (NFKB P65)/IL6 pathway in pregnant mice.
    Zhang WS, Xie QS, Wu XH, Liang QH.

    05/21/2011
    The mRNA and protein expressions of NMBR reach a peak at the onset of labor.

    [Expression of NMBR in myometrium in pregnant mice at different gestational ages and its relation with parturition].
    Zhang W, Xie Q, Wu Z, Wu X, Liang Q.

    04/30/2011
    disruption of the neuromedin B receptor pathway did not change body weight homeostasis in female mice fed a normolipid diet

    Female mice target deleted for the neuromedin B receptor have partial resistance to diet-induced obesity.
    Paula GS, Souza LL, Cabanelas A, Bloise FF, Mello-Coelho V, Wada E, Ortiga-Carvalho TM, Oliveira KJ, Pazos-Moura CC., Free PMC Article

    08/2/2010
    Selectivity of NMBR for neuromedin B over the gastrin-releasing peptide receptor depends primarily on differences in amino acids in the third extracellular domains of the receptors and in the adjacent upper fifth transmembrane region of the two receptors.

    Molecular basis for the selectivity of the mammalian bombesin peptide, neuromedin B, for its receptor.
    González N, Nakagawa T, Mantey SA, Sancho V, Uehara H, Katsuno T, Jensen RT., Free PMC Article

    01/21/2010
    NMB-R-deficient mice exhibited decreased behavior in both the L-D box and elevated plus maze tests.

    Role of bombesin (BN)-like peptides/receptors in emotional behavior by comparison of three strains of BN-like peptide receptor knockout mice.
    Yamada K, Santo-Yamada Y, Wada E, Wada K.

    01/21/2010
    NMBR and BRS-3 genes were expressed from embryonic days 13-16 and on multiple postnatal days for lungs

    Bombesin-like peptide receptor gene expression, regulation, and function in fetal murine lung.
    Shan L, Emanuel RL, Dewald D, Torday JS, Asokanathan N, Wada K, Wada E, Sunday ME.

    01/21/2010
    5-HT expression in the dorsal raphe (DR)nucleus is elevated in NMB-R-deficient mice. NMB/NMB-R may modulate 5-HT neuronal activity by affecting DR function.

    Decreased marble burying behavior in female mice lacking neuromedin-B receptor (NMB-R) implies the involvement of NMB/NMB-R in 5-HT neuron function.
    Yamada K, Wada E, Yamano M, Sun YJ, Ohara-Imaizumi M, Nagamatsu S, Wada K.

    01/21/2010
    Impaired memory in stressed neuromedin B receptor-deficient mice not consequence of changes in activity, anxiety, or pain response. NMB/NMB-R pathway may have role in regulating stress response via neural system controlling learning and memory.

    Stress-induced impairment of inhibitory avoidance learning in female neuromedin B receptor-deficient mice.
    Yamada K, Santo-Yamada Y, Wada K.

    01/21/2010
    firstprevious page of 1 nextlast