LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 158

Search options

  1. Article ; Online: Natural allelic variation modifies acute ethanol response phenotypes in wild strains of C. elegans.

    van Wijk, Marijke H / Davies, Andrew G / Sterken, Mark G / Mathies, Laura D / Quamme, Elizabeth C / Blackwell, GinaMari G / Riksen, Joost A G / Kammenga, Jan E / Bettinger, Jill C

    Alcohol, clinical & experimental research

    2023  Volume 47, Issue 8, Page(s) 1505–1517

    Abstract: Background: Genetic variation contributes to the likelihood that an individual will develop an alcohol use disorder (AUD). Traditional laboratory studies in animal models have elucidated the molecular pharmacology of ethanol, but laboratory-derived ... ...

    Abstract Background: Genetic variation contributes to the likelihood that an individual will develop an alcohol use disorder (AUD). Traditional laboratory studies in animal models have elucidated the molecular pharmacology of ethanol, but laboratory-derived genetic manipulations rarely model the naturally occurring genetic variation observed in wild populations. Rather, these manipulations are biased toward identifying genes of central importance in the phenotypes. Because changes in such genes can confer selective disadvantages, they are not ideal candidates for carrying AUD risk alleles in humans. We sought to exploit Caenorhabditis elegans to identify allelic variation existing in the wild that modulates ethanol response behaviors.
    Methods: We tested the acute ethanol responses of four strains recently isolated from the wild (JU1511, JU1926, JU1931, and JU1941) and 41 multiparental recombinant inbred lines (mpRILs) derived from them. We assessed locomotion at 10, 30, and 50 min on low and high ethanol concentrations. We performed principal component analyses (PCA) on the different phenotypes, tested for transgressive behavior, calculated heritability, and determined the correlations between behavioral responses.
    Results: We observed a range of responses to ethanol across the strains. We detected a low-concentration locomotor activation effect in some of the mpRILs not seen in the laboratory wild-type strain. PCA showed different ethanol response behaviors to be independent. We observed transgressive behavior for many of the measured phenotypes and found that multiple behaviors were uncorrelated. The average broad-sense heritability for all phenotypes was 23.2%.
    Conclusions: Genetic variation significantly affects multiple acute ethanol response behaviors, many of which are independent of one another. This suggests that the genetic variation captured by these strains likely affects multiple biological mechanisms through which ethanol acts. Further study of these strains may allow these distinct mechanisms to be identified.
    Language English
    Publishing date 2023-07-10
    Publishing country United States
    Document type Journal Article
    ISSN 2993-7175
    ISSN (online) 2993-7175
    DOI 10.1111/acer.15139
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Book ; Online: Natural variation on ChrI and ChrIV linked to locomotion activation in response to ethanol in C. elegans

    van Wijk, M.H. / Quamme, Elizabeth / Davies, Andrew G. / Riksen, J.A.G. / Sterken, M.G. / Kammenga, J.E. / Bettinger, Jill

    2023  

    Abstract: Alcohol use disorder is a global problem, with 50% of the risk determined by genetics. The acute physiological response to alcohol is a reliable predictor of AUD risk. Identifying genes and pathways that modulate acute ethanol responses is essential to ... ...

    Abstract Alcohol use disorder is a global problem, with 50% of the risk determined by genetics. The acute physiological response to alcohol is a reliable predictor of AUD risk. Identifying genes and pathways that modulate acute ethanol responses is essential to understanding the molecular basis of alcohol use disorder. Acute ethanol responses are conserved across species, including nematodes. Therefore, natural variation in Caenorhabditis elegans provides an opportunity to link wild alleles to acute ethanol response behaviors. Here, multi-parent recombinant inbred lines were behaviorally characterized in an ethanol response locomotion assay. Animals were continuously exposed to 0 mM, 200 mM, or 400 mM exogenous ethanol and tracked at 10, 30, and 50 minutes. Initial sensitivity, acute functional tolerance, and low concentration locomotor activation had narrow sense heritabilities of 0.28, 0.13, and 0.36, respectively, indicating that the observed phenotypic variance can be partly explained by additive genetics. QTL mapping identified two QTL for low concentration locomotor activation, which together explain 45.5% of the observed phenotypic variance in this population. The validation of these QTL using introgression lines and subsequent candidate prioritization will hopefully lead to the identification of genes that modulate low concentration locomotor activation in wild nematode populations.
    Keywords Life Science
    Language English
    Publishing country nl
    Document type Book ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  3. Article ; Online: Natural allelic variation modifies acute ethanol response phenotypes in wild strains of C. elegans

    van Wijk, Marijke H. / Davies, Andrew G. / Sterken, Mark G. / Mathies, Laura D. / Quamme, Elizabeth C. / Blackwell, Ginamari G. / Riksen, Joost A.G. / Kammenga, Jan E. / Bettinger, Jill C.

    Alcoholism : Clinical and Experimental Research

    2023  Volume 47, Issue 8

    Abstract: Background Genetic variation contributes to the likelihood that an individual will develop an alcohol use disorder (AUD). Traditional laboratory studies in animal models have elucidated the molecular pharmacology of ethanol, but laboratory-derived ... ...

    Abstract Background Genetic variation contributes to the likelihood that an individual will develop an alcohol use disorder (AUD). Traditional laboratory studies in animal models have elucidated the molecular pharmacology of ethanol, but laboratory-derived genetic manipulations rarely model the naturally occurring genetic variation observed in wild populations. Rather, these manipulations are biased toward identifying genes of central importance in the phenotypes. Because changes in such genes can confer selective disadvantages, they are not ideal candidates for carrying AUD risk alleles in humans. We sought to exploit Caenorhabditis elegans to identify allelic variation existing in the wild that modulates ethanol response behaviors.MethodsWe tested the acute ethanol responses of four strains recently isolated from the wild (JU1511, JU1926, JU1931, and JU1941) and 41 multiparental recombinant inbred lines (mpRILs) derived from them. We assessed locomotion at 10, 30, and 50 min on low and high ethanol concentrations. We performed principal component analyses (PCA) on the different phenotypes, tested for transgressive behavior, calculated heritability, and determined the correlations between behavioral responses.ResultsWe observed a range of responses to ethanol across the strains. We detected a low-concentration locomotor activation effect in some of the mpRILs not seen in the laboratory wild-type strain. PCA showed different ethanol response behaviors to be independent. We observed transgressive behavior for many of the measured phenotypes and found that multiple behaviors were uncorrelated. The average broad-sense heritability for all phenotypes was 23.2%.ConclusionsGenetic variation significantly affects multiple acute ethanol response behaviors, many of which are independent of one another. This suggests that the genetic variation captured by these strains likely affects multiple biological mechanisms through which ethanol acts. Further study of these strains may allow these distinct mechanisms to be identified.
    Keywords Life Science
    Subject code 612
    Language English
    Publishing country nl
    Document type Article ; Online
    ZDB-ID 428999-7
    ISSN 1530-0277 ; 0145-6008
    ISSN (online) 1530-0277
    ISSN 0145-6008
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  4. Article ; Online: Modeling Performance of Open Surgical Cases.

    Azari, David P / Frasier, Lane L / Miller, Brady L / Pavuluri Quamme, Sudha R / Le, Brian V / Greenberg, Caprice C / Radwin, Robert G

    Simulation in healthcare : journal of the Society for Simulation in Healthcare

    2021  Volume 16, Issue 6, Page(s) e188–e193

    Abstract: Introduction: Previous efforts used digital video to develop computer-generated assessments of surgical hand motion economy and fluidity of motion. This study tests how well previously trained assessment models match expert ratings of suturing and tying ...

    Abstract Introduction: Previous efforts used digital video to develop computer-generated assessments of surgical hand motion economy and fluidity of motion. This study tests how well previously trained assessment models match expert ratings of suturing and tying video clips recorded in a new operating room (OR) setting.
    Methods: Enabled through computer vision of the hands, this study tests the applicability of assessments born out of benchtop simulations to in vivo suturing and tying tasks recorded in the OR.
    Results: Compared with expert ratings, computer-generated assessments for fluidity of motion (slope = 0.83, intercept = 1.77, R2 = 0.55) performed better than motion economy (slope = 0.73, intercept = 2.04, R2 = 0.49), although 85% of ratings for both models were within ±2 of the expert response. Neither assessment performed as well in the OR as they did on the training data. Assessments were sensitive to changing hand postures, dropped ligatures, and poor tissue contact-features typically missing from training data. Computer-generated assessment of OR tasks was contingent on a clear, consistent view of both surgeon's hands.
    Conclusions: Computer-generated assessment may help provide formative feedback during deliberate practice, albeit with greater variability in the OR compared with benchtop simulations. Future work will benefit from expanded available bimanual video records.
    MeSH term(s) Clinical Competence ; Humans ; Operating Rooms ; Suture Techniques
    Language English
    Publishing date 2021-12-01
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2223429-9
    ISSN 1559-713X ; 1559-2332
    ISSN (online) 1559-713X
    ISSN 1559-2332
    DOI 10.1097/SIH.0000000000000544
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article ; Online: Transcriptional analysis of the response of C. elegans to ethanol exposure.

    Sterken, Mark G / van Wijk, Marijke H / Quamme, Elizabeth C / Riksen, Joost A G / Carnell, Lucinda / Mathies, Laura D / Davies, Andrew G / Kammenga, Jan E / Bettinger, Jill C

    Scientific reports

    2021  Volume 11, Issue 1, Page(s) 10993

    Abstract: Ethanol-induced transcriptional changes underlie important physiological responses to ethanol that are likely to contribute to the addictive properties of the drug. We examined the transcriptional responses of Caenorhabditis elegans across a timecourse ... ...

    Abstract Ethanol-induced transcriptional changes underlie important physiological responses to ethanol that are likely to contribute to the addictive properties of the drug. We examined the transcriptional responses of Caenorhabditis elegans across a timecourse of ethanol exposure, between 30 min and 8 h, to determine what genes and genetic pathways are regulated in response to ethanol in this model. We found that short exposures to ethanol (up to 2 h) induced expression of metabolic enzymes involved in metabolizing ethanol and retinol, while longer exposure (8 h) had much more profound effects on the transcriptome. Several genes that are known to be involved in the physiological response to ethanol, including direct ethanol targets, were regulated at 8 h of exposure. This longer exposure to ethanol also resulted in the regulation of genes involved in cilia function, which is consistent with an important role for the effects of ethanol on cilia in the deleterious effects of chronic ethanol consumption in humans. Finally, we found that food deprivation for an 8-h period induced gene expression changes that were somewhat ameliorated by the presence of ethanol, supporting previous observations that worms can use ethanol as a calorie source.
    MeSH term(s) Alcohol Drinking ; Animals ; Caenorhabditis elegans ; Ethanol ; Transcriptome
    Chemical Substances Ethanol (3K9958V90M)
    Language English
    Publishing date 2021-05-26
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-021-90282-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article ; Online: A biobehavioral intervention to enhance recovery following hematopoietic cell transplantation: Protocol for a feasibility and acceptability randomized control trial.

    Kirvin-Quamme, Andrew / Rumble, Meredith E / Cadmus-Bertram, Lisa / Juckett, Mark B / Rathouz, Paul J / Schell, Gwynneth / Callander, Natalie S / Hematti, Peiman / Costanzo, Erin S

    Contemporary clinical trials communications

    2022  Volume 28, Page(s) 100938

    Abstract: Background: Insomnia, fatigue, and depression are among the most persistent and distressing concerns for hematologic cancer patients recovering from hematopoietic cell transplantation (HCT). This study will evaluate a novel behavioral intervention, : ... ...

    Abstract Background: Insomnia, fatigue, and depression are among the most persistent and distressing concerns for hematologic cancer patients recovering from hematopoietic cell transplantation (HCT). This study will evaluate a novel behavioral intervention,
    Methods: The protocol herein evaluates the feasibility and acceptability of ReSET by conducting a pilot randomized controlled trial to compare the intervention with usual care. Adults undergoing HCT will be randomly assigned to ReSET or usual care. The ReSET arm will receive 3 face-to-face sessions and telephone coaching delivered in an individual format tailored to each patient. Patient-reported insomnia, fatigue, and depression will be the primary outcome measures. Actigraphy will be used to objectively quantify rest-activity patterns. Semi-structured interviews will evaluate participant satisfaction with ReSET. The goals are to determine: (1) participant satisfaction with and acceptability of the behavioral techniques; (2) facilitator fidelity and participant uptake of key intervention components; (3) ability to recruit, retain, and collect complete data from participants; (4) participant willingness to be randomized and acceptability of the control condition; and (5) validity and acceptability of the assessment strategy.
    Conclusion: The overarching goal is to optimize recovery following HCT with a brief, non-invasive intervention that can be implemented as a part of routine clinical care.
    Language English
    Publishing date 2022-05-28
    Publishing country Netherlands
    Document type Journal Article
    ISSN 2451-8654
    ISSN (online) 2451-8654
    DOI 10.1016/j.conctc.2022.100938
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  7. Article ; Online: Transcriptional analysis of the response of C. elegans to ethanol exposure

    Mark G. Sterken / Marijke H. van Wijk / Elizabeth C. Quamme / Joost A. G. Riksen / Lucinda Carnell / Laura D. Mathies / Andrew G. Davies / Jan E. Kammenga / Jill C. Bettinger

    Scientific Reports, Vol 11, Iss 1, Pp 1-

    2021  Volume 12

    Abstract: Abstract Ethanol-induced transcriptional changes underlie important physiological responses to ethanol that are likely to contribute to the addictive properties of the drug. We examined the transcriptional responses of Caenorhabditis elegans across a ... ...

    Abstract Abstract Ethanol-induced transcriptional changes underlie important physiological responses to ethanol that are likely to contribute to the addictive properties of the drug. We examined the transcriptional responses of Caenorhabditis elegans across a timecourse of ethanol exposure, between 30 min and 8 h, to determine what genes and genetic pathways are regulated in response to ethanol in this model. We found that short exposures to ethanol (up to 2 h) induced expression of metabolic enzymes involved in metabolizing ethanol and retinol, while longer exposure (8 h) had much more profound effects on the transcriptome. Several genes that are known to be involved in the physiological response to ethanol, including direct ethanol targets, were regulated at 8 h of exposure. This longer exposure to ethanol also resulted in the regulation of genes involved in cilia function, which is consistent with an important role for the effects of ethanol on cilia in the deleterious effects of chronic ethanol consumption in humans. Finally, we found that food deprivation for an 8-h period induced gene expression changes that were somewhat ameliorated by the presence of ethanol, supporting previous observations that worms can use ethanol as a calorie source.
    Keywords Medicine ; R ; Science ; Q
    Subject code 570 ; 660
    Language English
    Publishing date 2021-05-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  8. Article: Chlorpromazine activates chloride currents in Xenopus oocytes.

    Quamme, G A

    Biochimica et biophysica acta

    1997  Volume 1324, Issue 1, Page(s) 18–26

    Abstract: Xenopus oocytes are frequently used for in vivo expression of DNA and RNA, especially those encoding ion channel proteins. Accordingly, it is important to understand the expression and control of endogenous conductances. Ionic currents were studied in ... ...

    Abstract Xenopus oocytes are frequently used for in vivo expression of DNA and RNA, especially those encoding ion channel proteins. Accordingly, it is important to understand the expression and control of endogenous conductances. Ionic currents were studied in native Xenopus oocytes with two-microelectrode voltage-clamp technique to characterize the actions of chlorpromazine (CPZ) and trifluroperazine (TFP), two widely used antipsychotic drugs. External application of CPZ or TFP markedly stimulated endogenous conductances in a dose-dependent and reversible fashion. The current-voltage (I-V) relationship was non linear and dependent on the presence of external chloride. The CPZ-activated currents were inhibited by Cl- channel blockers. Although the removal of external Ca2+ had no effect on CPZ-induced conductances, the injection of BAPTA, a Ca2+ chelator, abolished endogenous activity. Thapsigargin also inhibited channel activity suggesting that CPZ acts through intraoocyte Ca2+ release. The calmodulin inhibitors, calmidazolium and W-7, failed to mimic the action of CPZ. These data provide evidence for external or internal phenothiazine receptors which when activated by CPZ induces Ca(2+)-dependent Cl- channel activity in endogenous native oocytes.
    MeSH term(s) Animals ; Antipsychotic Agents/pharmacology ; Calcium/metabolism ; Calcium-Transporting ATPases/antagonists & inhibitors ; Calmodulin/physiology ; Cell Membrane/physiology ; Chelating Agents/pharmacology ; Chloride Channels/antagonists & inhibitors ; Chloride Channels/drug effects ; Chloride Channels/physiology ; Chlorpromazine/pharmacology ; Egtazic Acid/analogs & derivatives ; Egtazic Acid/pharmacology ; Enzyme Inhibitors/pharmacology ; Oocytes ; Patch-Clamp Techniques ; Receptors, Dopamine/metabolism ; Thapsigargin/pharmacology ; Trifluoperazine/pharmacology ; Xenopus
    Chemical Substances Antipsychotic Agents ; Calmodulin ; Chelating Agents ; Chloride Channels ; Enzyme Inhibitors ; Receptors, Dopamine ; phenothiazine receptor ; Trifluoperazine (214IZI85K3) ; Egtazic Acid (526U7A2651) ; Thapsigargin (67526-95-8) ; Calcium-Transporting ATPases (EC 3.6.3.8) ; 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid (K22DDW77C0) ; Calcium (SY7Q814VUP) ; Chlorpromazine (U42B7VYA4P)
    Language English
    Publishing date 1997-02-21
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 60-7
    ISSN 1879-2596 ; 1879-260X ; 1872-8006 ; 1879-2642 ; 1879-2618 ; 1879-2650 ; 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    ISSN (online) 1879-2596 ; 1879-260X ; 1872-8006 ; 1879-2642 ; 1879-2618 ; 1879-2650
    ISSN 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    DOI 10.1016/s0005-2736(96)00205-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  9. Article: Renal magnesium handling: new insights in understanding old problems.

    Quamme, G A

    Kidney international

    1997  Volume 52, Issue 5, Page(s) 1180–1195

    Abstract: Recent research has provided new concepts in our understanding of renal magnesium handling. Although the majority of the filtered magnesium is reabsorbed within the loop of Henle, it is now recognized that the distal tubule also plays an important role ... ...

    Abstract Recent research has provided new concepts in our understanding of renal magnesium handling. Although the majority of the filtered magnesium is reabsorbed within the loop of Henle, it is now recognized that the distal tubule also plays an important role in magnesium conservation. Magnesium absorption within the cTAL segment of the loop is passive and dependent on the transepithelial voltage. Magnesium transport in the DCT is active and transcellular in nature. Many of the hormonal (PTH, calcitonin, glucagon, AVP) and nonhormonal (magnesium-restriction, acid-base changes, potassium-depletion) influences that affect magnesium transport within the cTAL similarly alter magnesium absorption within the DCT. However, the cellular mechanisms are different. Actions within the loop affect either the transepithelial voltage or the paracellular permeability. Influences acting in the DCT involve changes in active transcellular transport either Mg2+ entry across the apical membrane or Mg2+ exit from the basolateral side. These transport processes are fruitful areas for future research. An additional regulatory control has recently been recognized that involves an extracellular Ca2+/Mg(2+)-sensing receptor. This receptor is present in the basolateral membrane of the TAL and DCT and modulates magnesium and calcium conservation with elevation in plasma divalent cation concentration. Further studies are warranted to determine the physiological role of the Ca2+/Mg(2+)-sensing receptor, but activating and inactivating mutations have been described that result in renal magnesium-wasting and hypermagnesemia, respectively. All of these receptor-mediated controls change calcium absorption in addition to magnesium transport. Selective magnesium control is through intrinsic control of Mg2+ entry into distal tubule cells. The cellular mechanisms that intrinsically regulate magnesium transport have yet to be described. Familial diseases associated with renal magnesium-wasting provide a unique opportunity to study these intrinsic controls. Loop diuretics such as furosemide increase magnesium excretion by virtue of its effects on the transepithelial voltage thereby inhibiting passive magnesium absorption. Distally acting diuretics, like amiloride and chlorothiazide, enhance Mg2+ entry into DCT cells. Amiloride may be used as a magnesium-conserving diuretic whereas chlorothiazide may lead to potassium-depletion that compromises renal magnesium absorption. Patients with Bartter's and Gitelman's syndromes, diseases of salt transport in the loop and distal tubule, respectively, are associated with disturbances in renal magnesium handling. These may provide useful lessons in understanding segmental control of magnesium reabsorption. Metabolic acidosis diminishes magnesium absorption in MDCT cells by protonation of the Mg2+ entry pathway. Metabolic alkalosis increases magnesium permeability across the cTAL paracellular pathway and stimulates Mg2+ entry into DCT cells. Again, these changes are likely due to protonation of charges along the paracellular pathway of the cTAL and the putative Mg2+ channel of the DCT. Cellular potassium-depletion diminishes the voltage-dependent magnesium absorption in the TAL and Mg2+ entry into MDCT cells. However, the relationship between potassium and magnesium balance is far from clear. For instance, magnesium-wasting is more commonly found in patients with Gitelman's disease than Bartter's but both have hypokalemia. Further studies are needed to sort out these discrepancies. Phosphate deficiency also decreases Mg2+ uptake in distal cells but it apparently does so by mechanisms other than those observed in potassium depletion. Accordingly, potassium depletion, phosphate deficiency, and metabolic acidosis may be additive. The means by which cellular potassium and phosphate alter magnesium handling are unclear. Research in the nineties has increased our understanding of renal magnesium transport and regulation, but there are many in
    MeSH term(s) Absorption ; Acid-Base Imbalance/metabolism ; Animals ; Calcium/blood ; Diuretics/pharmacology ; Humans ; Hypokalemia/metabolism ; Hypophosphatemia/metabolism ; Kidney Tubules/metabolism ; Magnesium/metabolism
    Chemical Substances Diuretics ; Magnesium (I38ZP9992A) ; Calcium (SY7Q814VUP)
    Language English
    Publishing date 1997-11
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 120573-0
    ISSN 1523-1755 ; 0085-2538
    ISSN (online) 1523-1755
    ISSN 0085-2538
    DOI 10.1038/ki.1997.443
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  10. Article ; Online: Transcriptional analysis of the response of C. elegans to ethanol exposure

    Sterken, M.G. / van Wijk, M.H. / Quamme, Elizabeth / Riksen, J.A.G. / Carnell, Lucinda / Mathies, Laura / Davies, A.E. / Kammenga, J.E. / Bettinger, Jill

    Scientific Reports

    2021  Volume 11

    Abstract: Ethanol-induced transcriptional changes underlie important physiological responses to ethanol that are likely to contribute to the addictive properties of the drug. We examined the transcriptional responses of Caenorhabditis elegans across a timecourse ... ...

    Abstract Ethanol-induced transcriptional changes underlie important physiological responses to ethanol that are likely to contribute to the addictive properties of the drug. We examined the transcriptional responses of Caenorhabditis elegans across a timecourse of ethanol exposure, between 30 min and 8 h, to determine what genes and genetic pathways are regulated in response to ethanol in this model. We found that short exposures to ethanol (up to 2 h) induced expression of metabolic enzymes involved in metabolizing ethanol and retinol, while longer exposure (8 h) had much more profound effects on the transcriptome. Several genes that are known to be involved in the physiological response to ethanol, including direct ethanol targets, were regulated at 8 h of exposure. This longer exposure to ethanol also resulted in the regulation of genes involved in cilia function, which is consistent with an important role for the effects of ethanol on cilia in the deleterious effects of chronic ethanol consumption in humans. Finally, we found that food deprivation for an 8-h period induced gene expression changes that were somewhat ameliorated by the presence of ethanol, supporting previous observations that worms can use ethanol as a calorie source.
    Keywords Life Science
    Subject code 570
    Language English
    Publishing country nl
    Document type Article ; Online
    ZDB-ID 2615211-3
    ISSN 2045-2322
    ISSN 2045-2322
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

To top