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Study · Animal study (in vivo) · mouse · 2011

18 results

Nr4a1 siRNA expression attenuates α-MSH regulated gene expression in 3T3-L1 adipocytes.

Wang SC, Myers SA, Eriksson NA, Fitzsimmons RL, Muscat GE

Molecular endocrinology (Baltimore, Md.)14 Jan 2011Cited by 19 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study18

11 results from studies that gave the peptide. No result from this study comes from people.

  1. 01AnimalAnimal study (in vivo)Mechanism

    In male C57BL/6J mice, intraperitoneal NDP-MSH significantly induced Nur77 mRNA in inguinal adipose tissue.

    In plain wordsIn male mice, NDP-MSH injected into the belly cavity significantly raised Nur77 gene activity in fat tissue.

    Outcome
    IncreaseNur77 mRNA in adipose tissue
    Study

    mousen: not reported in source

    C57 BL/6J male mice, inguinal adipose tissue
    Outcome group
    Receptor activity and mechanism · Metabolic and weight
    Studied dose
    Dose not stated · intraperitonealAs given in this study (mouse).

    Source sentences

    Summary
    In vivo, ip administration of NDP-MSH to C57 BL/6J (male) mice significantly induced the expression of the mRNA encoding Nur77 and increased IL-6, Cox2, Pck1, and Pdk4 mRNA expression in (inguinal) adipose tissue.
  2. 02AnimalAnimal study (in vivo)Mechanism

    In male C57BL/6J mice, intraperitoneal NDP-MSH increased IL-6 mRNA expression in inguinal adipose tissue.

    In plain wordsIn male mice, NDP-MSH injected into the belly cavity raised IL-6 gene activity in fat tissue.

    Outcome
    IncreaseIL-6 mRNA in adipose tissue
    Study

    mousen: not reported in source

    C57 BL/6J male mice, inguinal adipose tissue
    Outcome group
    Receptor activity and mechanism · Metabolic and weight
    Studied dose
    Dose not stated · intraperitonealAs given in this study (mouse).

    Source sentences

    Summary
    In vivo, ip administration of NDP-MSH to C57 BL/6J (male) mice significantly induced the expression of the mRNA encoding Nur77 and increased IL-6, Cox2, Pck1, and Pdk4 mRNA expression in (inguinal) adipose tissue.
  3. 03AnimalAnimal study (in vivo)Mechanism

    In male C57BL/6J mice, intraperitoneal NDP-MSH increased Cox2 mRNA expression in inguinal adipose tissue.

    In plain wordsIn male mice, NDP-MSH injected into the belly cavity raised Cox2 gene activity in fat tissue.

    Outcome
    IncreaseCox2 mRNA in adipose tissue
    Study

    mousen: not reported in source

    C57 BL/6J male mice, inguinal adipose tissue
    Outcome group
    Receptor activity and mechanism · Metabolic and weight
    Studied dose
    Dose not stated · intraperitonealAs given in this study (mouse).

    Source sentences

    Summary
    In vivo, ip administration of NDP-MSH to C57 BL/6J (male) mice significantly induced the expression of the mRNA encoding Nur77 and increased IL-6, Cox2, Pck1, and Pdk4 mRNA expression in (inguinal) adipose tissue.
  4. 04AnimalAnimal study (in vivo)Mechanism

    In male C57BL/6J mice, intraperitoneal NDP-MSH increased Pck1 mRNA expression in inguinal adipose tissue.

    In plain wordsIn male mice, NDP-MSH injected into the belly cavity raised Pck1 gene activity in fat tissue.

    Outcome
    IncreasePck1 mRNA in adipose tissue
    Study

    mousen: not reported in source

    C57 BL/6J male mice, inguinal adipose tissue
    Outcome group
    Receptor activity and mechanism · Metabolic and weight
    Studied dose
    Dose not stated · intraperitonealAs given in this study (mouse).

    Source sentences

    Summary
    In vivo, ip administration of NDP-MSH to C57 BL/6J (male) mice significantly induced the expression of the mRNA encoding Nur77 and increased IL-6, Cox2, Pck1, and Pdk4 mRNA expression in (inguinal) adipose tissue.
  5. 05AnimalAnimal study (in vivo)Mechanism

    In male C57BL/6J mice, intraperitoneal NDP-MSH increased Pdk4 mRNA expression in inguinal adipose tissue.

    In plain wordsIn male mice, NDP-MSH injected into the belly cavity raised Pdk4 gene activity in fat tissue.

    Outcome
    IncreasePdk4 mRNA in adipose tissue
    Study

    mousen: not reported in source

    C57 BL/6J male mice, inguinal adipose tissue
    Outcome group
    Receptor activity and mechanism · Metabolic and weight
    Studied dose
    Dose not stated · intraperitonealAs given in this study (mouse).

    Source sentences

    Summary
    In vivo, ip administration of NDP-MSH to C57 BL/6J (male) mice significantly induced the expression of the mRNA encoding Nur77 and increased IL-6, Cox2, Pck1, and Pdk4 mRNA expression in (inguinal) adipose tissue.
  6. 06LabIn vitro (cells)Mechanism

    In differentiated 3T3-L1 adipocytes, NDP-MSH preferentially induced expression of the NR4A subgroup of nuclear receptors, but not other nuclear receptor superfamily members.

    In plain wordsIn mouse fat cells in a dish, NDP-MSH raised the activity of NR4A genes but not of other nuclear receptor genes.

    Outcome
    IncreaseExpression of NR4A subgroup nuclear receptors
    Study

    mousen: not reported in source

    Differentiated 3T3-L1 adipocytes
    Outcome group
    Receptor activity and mechanism · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    We have shown that NDP-MSH strikingly and preferentially induces the expression of the NR4A subgroup (but not any other members of the NR superfamily) in differentiated 3T3-L1 adipocytes.
  7. 07LabIn vitro (cells)Mechanism

    In differentiated 3T3-L1 adipocytes, NDP-MSH treatment induced Il-6 mRNA.

    In plain wordsIn mouse fat cells in a dish, NDP-MSH raised Il-6 gene activity.

    Outcome
    IncreaseIl-6 mRNA induction
    Study

    mousen: not reported in source

    Differentiated 3T3-L1 adipocytes
    Outcome group
    Receptor activity and mechanism · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Utilization of quantitative PCR on custom-designed metabolic TaqMan low-density arrays identified the concomitant and marked induction of the mRNAs encoding Il-6, Cox2, Pdk4, and Pck-1 after NDP-MSH treatment.
  8. 08LabIn vitro (cells)Mechanism

    In differentiated 3T3-L1 adipocytes, NDP-MSH treatment induced Cox2 mRNA.

    In plain wordsIn mouse fat cells in a dish, NDP-MSH raised Cox2 gene activity.

    Outcome
    IncreaseCox2 mRNA induction
    Study

    mousen: not reported in source

    Differentiated 3T3-L1 adipocytes
    Outcome group
    Receptor activity and mechanism · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Utilization of quantitative PCR on custom-designed metabolic TaqMan low-density arrays identified the concomitant and marked induction of the mRNAs encoding Il-6, Cox2, Pdk4, and Pck-1 after NDP-MSH treatment.
  9. 09LabIn vitro (cells)Mechanism

    In differentiated 3T3-L1 adipocytes, NDP-MSH treatment induced Pdk4 mRNA.

    In plain wordsIn mouse fat cells in a dish, NDP-MSH raised Pdk4 gene activity.

    Outcome
    IncreasePdk4 mRNA induction
    Study

    mousen: not reported in source

    Differentiated 3T3-L1 adipocytes
    Outcome group
    Receptor activity and mechanism · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Utilization of quantitative PCR on custom-designed metabolic TaqMan low-density arrays identified the concomitant and marked induction of the mRNAs encoding Il-6, Cox2, Pdk4, and Pck-1 after NDP-MSH treatment.
  10. 10LabIn vitro (cells)Mechanism

    In differentiated 3T3-L1 adipocytes, NDP-MSH treatment induced Pck-1 mRNA.

    In plain wordsIn mouse fat cells in a dish, NDP-MSH raised Pck-1 gene activity.

    Outcome
    IncreasePck-1 mRNA induction
    Study

    mousen: not reported in source

    Differentiated 3T3-L1 adipocytes
    Outcome group
    Receptor activity and mechanism · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Utilization of quantitative PCR on custom-designed metabolic TaqMan low-density arrays identified the concomitant and marked induction of the mRNAs encoding Il-6, Cox2, Pdk4, and Pck-1 after NDP-MSH treatment.
  11. 11LabIn vitro (cells)Mechanism

    In differentiated 3T3-L1 adipocytes, the mRNA expression profiles induced by cAMP and NDP-MSH had unique but also overlapping properties.

    In plain wordsIn mouse fat cells in a dish, cAMP and NDP-MSH changed some of the same genes and some different genes.

    Outcome
    MixedGene expression profile of cAMP versus NDP-MSH
    Study

    mousen: not reported in source

    Differentiated 3T3-L1 adipocytes
    Outcome group
    Receptor activity and mechanism · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Similar experiments demonstrated that the mRNA expression profile induced by cAMP and NDP-MSH treatment displayed unique but also overlapping properties and suggested that melanocortin-mediated induction of gene expression involves cAMP-dependent and -independent signaling.

Studies that did not test the peptide alone7

In this study, Melanotan I (afamelanotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Melanotan I (afamelanotide).

  1. 12LabNot a test of Melanotan I (afamelanotide) aloneIn vitro (cells)Mechanism

    In differentiated 3T3-L1 adipocytes, Nr4a1/Nur77 siRNA suppressed the NDP-MSH-mediated induction of Nr4a1/Nur77.

    In plain wordsIn mouse fat cells in a dish, switching off Nur77 with siRNA reduced the NDP-MSH rise in Nur77.

    Outcome
    DecreaseNDP-MSH induction of Nr4a1/Nur77 with Nur77 siRNA
    Study

    mousen: not reported in source

    Differentiated 3T3-L1 adipocytes
    Outcome group
    Receptor activity and mechanism · Metabolic and weight

    Source sentences

    Summary
    Nr4a1/Nur77 small interfering RNA (siRNA) expression suppressed NDP-MSH-mediated induction of Nr4a1/Nur77 and Nr4a3/Nor-1

    In this study, Melanotan I (afamelanotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Melanotan I (afamelanotide).

  2. 13LabNot a test of Melanotan I (afamelanotide) aloneIn vitro (cells)Mechanism

    In differentiated 3T3-L1 adipocytes, Nr4a1/Nur77 siRNA suppressed the NDP-MSH-mediated induction of Nr4a3/Nor-1.

    In plain wordsIn mouse fat cells in a dish, switching off Nur77 with siRNA reduced the NDP-MSH rise in Nor-1.

    Outcome
    DecreaseNDP-MSH induction of Nr4a3/Nor-1 with Nur77 siRNA
    Study

    mousen: not reported in source

    Differentiated 3T3-L1 adipocytes
    Outcome group
    Receptor activity and mechanism · Metabolic and weight

    Source sentences

    Summary
    Nr4a1/Nur77 small interfering RNA (siRNA) expression suppressed NDP-MSH-mediated induction of Nr4a1/Nur77 and Nr4a3/Nor-1

    In this study, Melanotan I (afamelanotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Melanotan I (afamelanotide).

  3. 14LabNot a test of Melanotan I (afamelanotide) aloneIn vitro (cells)Mechanism

    In differentiated 3T3-L1 adipocytes, Nr4a1/Nur77 siRNA did not suppress the NDP-MSH-mediated induction of Nr4a2/Nurr1.

    In plain wordsIn mouse fat cells in a dish, switching off Nur77 with siRNA did not reduce the NDP-MSH rise in Nurr1.

    Outcome
    No significant changeNDP-MSH induction of Nr4a2/Nurr1 with Nur77 siRNA
    Study

    mousen: not reported in source

    Differentiated 3T3-L1 adipocytes
    Outcome group
    Receptor activity and mechanism · Metabolic and weight

    Source sentences

    Summary
    Nr4a1/Nur77 small interfering RNA (siRNA) expression suppressed NDP-MSH-mediated induction of Nr4a1/Nur77 and Nr4a3/Nor-1 (but not Nr4a2/Nurr1).

    In this study, Melanotan I (afamelanotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Melanotan I (afamelanotide).

  4. 15LabNot a test of Melanotan I (afamelanotide) aloneIn vitro (cells)Mechanism

    In differentiated 3T3-L1 adipocytes, Nur77 siRNA attenuated the NDP-MSH-mediated induction of Il-6 mRNA.

    In plain wordsIn mouse fat cells in a dish, switching off Nur77 with siRNA reduced the NDP-MSH rise in Il-6.

    Outcome
    DecreaseNDP-MSH induction of Il-6 mRNA with Nur77 siRNA
    Study

    mousen: not reported in source

    Differentiated 3T3-L1 adipocytes
    Outcome group
    Receptor activity and mechanism · Metabolic and weight

    Source sentences

    Summary
    Moreover, expression of the siRNA-attenuated NDP-MSH mediated induction of the mRNAs encoding Il-6, Cox2/Ptgs2, and Pck-1 expression.

    In this study, Melanotan I (afamelanotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Melanotan I (afamelanotide).

  5. 16LabNot a test of Melanotan I (afamelanotide) aloneIn vitro (cells)Mechanism

    In differentiated 3T3-L1 adipocytes, Nur77 siRNA attenuated the NDP-MSH-mediated induction of Cox2/Ptgs2 mRNA.

    In plain wordsIn mouse fat cells in a dish, switching off Nur77 with siRNA reduced the NDP-MSH rise in Cox2.

    Outcome
    DecreaseNDP-MSH induction of Cox2/Ptgs2 mRNA with Nur77 siRNA
    Study

    mousen: not reported in source

    Differentiated 3T3-L1 adipocytes
    Outcome group
    Receptor activity and mechanism · Metabolic and weight

    Source sentences

    Summary
    Moreover, expression of the siRNA-attenuated NDP-MSH mediated induction of the mRNAs encoding Il-6, Cox2/Ptgs2, and Pck-1 expression.

    In this study, Melanotan I (afamelanotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Melanotan I (afamelanotide).

  6. 17LabNot a test of Melanotan I (afamelanotide) aloneIn vitro (cells)Mechanism

    In differentiated 3T3-L1 adipocytes, Nur77 siRNA attenuated the NDP-MSH-mediated induction of Pck-1 mRNA.

    In plain wordsIn mouse fat cells in a dish, switching off Nur77 with siRNA reduced the NDP-MSH rise in Pck-1.

    Outcome
    DecreaseNDP-MSH induction of Pck-1 mRNA with Nur77 siRNA
    Study

    mousen: not reported in source

    Differentiated 3T3-L1 adipocytes
    Outcome group
    Receptor activity and mechanism · Metabolic and weight

    Source sentences

    Summary
    Moreover, expression of the siRNA-attenuated NDP-MSH mediated induction of the mRNAs encoding Il-6, Cox2/Ptgs2, and Pck-1 expression.

    In this study, Melanotan I (afamelanotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Melanotan I (afamelanotide).

  7. 18LabNot a test of Melanotan I (afamelanotide) aloneIn vitro (cells)Efficacy outcome

    In differentiated 3T3-L1 adipocytes, Nur77 siRNA expression attenuated NDP-MSH-mediated glucose uptake.

    In plain wordsIn mouse fat cells in a dish, switching off Nur77 with siRNA reduced the glucose uptake driven by NDP-MSH.

    Outcome
    DecreaseNDP-MSH-mediated glucose uptake with Nur77 siRNA
    Study

    mousen: not reported in source

    Differentiated 3T3-L1 adipocytes
    Outcome group
    Glycemic control · Metabolic and weight

    Source sentences

    Summary
    In addition, Nur77 siRNA expression attenuated NDP-MSH-mediated glucose uptake.

    In this study, Melanotan I (afamelanotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Melanotan I (afamelanotide).

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    13 Oct 2026, 21:44 UTC

    Study results updated

  2. Version 1

    13 Oct 2026, 16:31 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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