LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 101

Search options

  1. Article ; Online: Managing Iron Overload: A Gut Check.

    Garrick, Michael D

    The Journal of pharmacology and experimental therapeutics

    2023  Volume 386, Issue 1, Page(s) 1–3

    Abstract: Divalent metal transporter 1 (DMT1) is the major importer of ferrous iron at the apical surface of enterocytes in the duodenum. Multiple groups have tried to design specific inhibitors for DMT1 both to study its contributions to iron (and metal ion) ... ...

    Abstract Divalent metal transporter 1 (DMT1) is the major importer of ferrous iron at the apical surface of enterocytes in the duodenum. Multiple groups have tried to design specific inhibitors for DMT1 both to study its contributions to iron (and metal ion) homeostasis and to provide a pharmacological means to treat iron overload disorders like hereditary hemochromatosis and thalassemias. This task faces challenges because many tissues express DMT1 and DMT1 transports other metals adding to standard risks in making specific inhibitors. Xenon Pharmaceuticals have published several papers on their efforts. Their latest paper in this issue of the journal culminates their efforts with compounds named XEN601 and XEN602 but implies that these very effective inhibitors have sufficient toxicity for them to halt development. This Viewpoint evaluates their efforts and briefly considers alternative routes to the goal. SIGNIFICANCE STATEMENT: This Viewpoint briefly reviews the paper on inhibitors of DMT1 that appears in this issue of the journal and commends the effort and research utility of those developed by Xenon. The inhibitors have proven to be valuable research tools for studying metal ion homeostasis particularly for iron. If Xenon is ceasing to try to develop them for treatment of iron overload disorders, then new alternatives need to come to the fore.
    MeSH term(s) Humans ; Iron Overload/drug therapy ; Iron Overload/metabolism ; Iron/metabolism ; Biological Transport ; Iron-Binding Proteins/metabolism ; Enterocytes/metabolism
    Chemical Substances Iron (E1UOL152H7) ; Iron-Binding Proteins
    Language English
    Publishing date 2023-03-02
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 3106-9
    ISSN 1521-0103 ; 0022-3565
    ISSN (online) 1521-0103
    ISSN 0022-3565
    DOI 10.1124/jpet.123.001645
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Correction to: Iron chelation may harm patients with COVID-19.

    Garrick, Michael D / Ghio, Andrew J

    European journal of clinical pharmacology

    2021  Volume 77, Issue 8, Page(s) 1255

    Language English
    Publishing date 2021-03-15
    Publishing country Germany
    Document type Published Erratum
    ZDB-ID 121960-1
    ISSN 1432-1041 ; 0031-6970
    ISSN (online) 1432-1041
    ISSN 0031-6970
    DOI 10.1007/s00228-021-03124-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Iron chelation may harm patients with COVID-19.

    Garrick, Michael D / Ghio, Andrew J

    European journal of clinical pharmacology

    2020  Volume 77, Issue 2, Page(s) 265–266

    MeSH term(s) COVID-19 ; Humans ; Iron Chelating Agents ; SARS-CoV-2
    Chemical Substances Iron Chelating Agents
    Keywords covid19
    Language English
    Publishing date 2020-09-01
    Publishing country Germany
    Document type Letter ; Comment
    ZDB-ID 121960-1
    ISSN 1432-1041 ; 0031-6970
    ISSN (online) 1432-1041
    ISSN 0031-6970
    DOI 10.1007/s00228-020-02987-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  4. Article: Corrigendum: Iron and Cadmium Entry Into Renal Mitochondria: Physiological and Toxicological Implications.

    Thévenod, Frank / Lee, Wing-Kee / Garrick, Michael D

    Frontiers in cell and developmental biology

    2021  Volume 9, Page(s) 687810

    Abstract: This corrects the article DOI: 10.3389/fcell.2020.00848.]. ...

    Abstract [This corrects the article DOI: 10.3389/fcell.2020.00848.].
    Language English
    Publishing date 2021-04-19
    Publishing country Switzerland
    Document type Published Erratum
    ZDB-ID 2737824-X
    ISSN 2296-634X
    ISSN 2296-634X
    DOI 10.3389/fcell.2021.687810
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article: Iron and Cadmium Entry Into Renal Mitochondria: Physiological and Toxicological Implications.

    Thévenod, Frank / Lee, Wing-Kee / Garrick, Michael D

    Frontiers in cell and developmental biology

    2020  Volume 8, Page(s) 848

    Abstract: Regulation of body fluid homeostasis is a major renal function, occurring largely through epithelial solute transport in various nephron segments driven by ... ...

    Abstract Regulation of body fluid homeostasis is a major renal function, occurring largely through epithelial solute transport in various nephron segments driven by Na
    Language English
    Publishing date 2020-09-02
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2737824-X
    ISSN 2296-634X
    ISSN 2296-634X
    DOI 10.3389/fcell.2020.00848
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article ; Online: Iron chelation may harm patients with COVID-19

    Garrick, Michael D. / Ghio, Andrew J.

    European Journal of Clinical Pharmacology ; ISSN 0031-6970 1432-1041

    2020  

    Keywords Pharmacology (medical) ; Pharmacology ; General Medicine ; covid19
    Language English
    Publisher Springer Science and Business Media LLC
    Publishing country us
    Document type Article ; Online
    DOI 10.1007/s00228-020-02987-w
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  7. Article ; Online: Corrigendum

    Frank Thévenod / Wing-Kee Lee / Michael D. Garrick

    Frontiers in Cell and Developmental Biology, Vol

    Iron and Cadmium Entry Into Renal Mitochondria: Physiological and Toxicological Implications

    2021  Volume 9

    Keywords reactive oxygen species ; divalent metal transporter 1 ; ionic mimicry ; manganese ; copper ; nephrotoxicity ; Biology (General) ; QH301-705.5
    Language English
    Publishing date 2021-04-01T00:00:00Z
    Publisher Frontiers Media S.A.
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  8. Article ; Online: Fetal factors disrupt placental and maternal iron homeostasis in murine β-thalassemia.

    Yu, Yang / Woloshun, Regina R / Lee, Jennifer K / Ebea, Pearl Onuwa / Zhu, Sean / Nemeth, Elizabeta / Garrick, Laura M / Garrick, Michael D / Collins, James F

    Blood

    2023  Volume 142, Issue 2, Page(s) 185–196

    Abstract: Pregnancy rates in β-thalassemia are increasing but the risk of complications is higher; thus, better understanding of maternal and fetal iron homeostasis in this disorder is needed. HbbTh3/+ (Th3/+) mice model human β-thalassemia. Both the murine and ... ...

    Abstract Pregnancy rates in β-thalassemia are increasing but the risk of complications is higher; thus, better understanding of maternal and fetal iron homeostasis in this disorder is needed. HbbTh3/+ (Th3/+) mice model human β-thalassemia. Both the murine and human diseases are characterized by low hepcidin, high iron absorption, and tissue iron overload, with concurrent anemia. We hypothesized that disordered iron metabolism in pregnant Th3/+ mice would negatively affect their unborn offspring. The experimental design included these groups: wild-type (WT) dams carrying WT fetuses (WT1); WT dams carrying WT and Th3/+ fetuses (WT2); Th3/+ dams carrying WT and Th3/+ fetuses (Th3/+); and age-matched, nonpregnant adult females. Serum hepcidin was low, and mobilization of splenic and hepatic storage iron was enhanced in all 3 groups of experimental dams. Intestinal 59Fe absorption was lower in Th3/+ dams (as compared with WT1/2 dams) but splenic 59Fe uptake was higher. Th3/+ dams had hyperferremia, which led to fetal and placenta iron loading, fetal growth restriction, and placentomegaly. Notably, Th3/+ dams loaded Th3/+ and WT fetuses, with the latter situation more closely mirroring human circumstances when mothers with thalassemia have relatively unaffected (thalassemia trait) offspring. Iron-related oxidative stress likely contributed to fetal growth impairment; enhanced placental erythropoiesis is a probable cause of placental enlargement. Moreover, high fetal liver iron transactivated Hamp; fetal hepcidin downregulated placental ferroportin expression, limiting placental iron flux and thus mitigating fetal iron loading. Whether gestational iron loading occurs in human thalassemic pregnancy, when blood transfusion can further elevate serum iron, is worth consideration.
    MeSH term(s) Mice ; Female ; Humans ; Pregnancy ; Animals ; Hepcidins ; beta-Thalassemia/metabolism ; Placenta/metabolism ; Iron/metabolism ; Fetus/metabolism ; Homeostasis
    Chemical Substances Hepcidins ; Iron (E1UOL152H7)
    Language English
    Publishing date 2023-05-06
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 80069-7
    ISSN 1528-0020 ; 0006-4971
    ISSN (online) 1528-0020
    ISSN 0006-4971
    DOI 10.1182/blood.2022018839
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  9. Article ; Online: Animal Models of Normal and Disturbed Iron and Copper Metabolism.

    Wang, Xiaoyu / Garrick, Michael D / Collins, James F

    The Journal of nutrition

    2019  Volume 149, Issue 12, Page(s) 2085–2100

    Abstract: Research on the interplay between iron and copper metabolism in humans began to flourish in the mid-20th century, and diseases associated with dysregulated homeostasis of these essential trace minerals are common even today. Iron deficiency is the most ... ...

    Abstract Research on the interplay between iron and copper metabolism in humans began to flourish in the mid-20th century, and diseases associated with dysregulated homeostasis of these essential trace minerals are common even today. Iron deficiency is the most frequent cause of anemia worldwide, leading to significant morbidity, particularly in developing countries. Iron overload is also quite common, usually being the result of genetic mutations which lead to inappropriate expression of the iron-regulatory hormone hepcidin. Perturbations of copper homeostasis in humans have also been described, including rare genetic conditions which lead to severe copper deficiency (Menkes disease) or copper overload (Wilson disease). Historically, the common laboratory rat (Rattus norvegicus) was the most frequently utilized species to model human physiology and pathophysiology. Recently, however, the development of genetic-engineering technology combined with the worldwide availability of numerous genetically homogenous (i.e., inbred) mouse strains shifted most research on iron and copper metabolism to laboratory mice. This created new opportunities to understand the function of individual genes in the context of a living animal, but thoughtful consideration of whether mice are the most appropriate models of human pathophysiology was not necessarily involved. Given this background, this review is intended to provide a guide for future research on iron- and copper-related disorders in humans. Generation of complementary experimental models in rats, swine, and other mammals is now facile given the advent of newer genetic technologies, thus providing the opportunity to accelerate the identification of pathogenic mechanisms and expedite the development of new treatments to mitigate these important human disorders.
    MeSH term(s) Anemia, Iron-Deficiency/genetics ; Anemia, Iron-Deficiency/metabolism ; Animals ; Copper/metabolism ; Diet ; Iron/metabolism ; Models, Animal
    Chemical Substances Copper (789U1901C5) ; Iron (E1UOL152H7)
    Language English
    Publishing date 2019-08-29
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Review
    ZDB-ID 218373-0
    ISSN 1541-6100 ; 0022-3166
    ISSN (online) 1541-6100
    ISSN 0022-3166
    DOI 10.1093/jn/nxz172
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top