Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

[Endothelin, EDRF, CGRP].

Y Terada1, K Tomita, F Marumo

  • 1Second Department of Internal Medicine, Tokyo Medical and Dental University.

Nihon Rinsho. Japanese Journal of Clinical Medicine
|December 1, 1992
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Hyponatremia with consciousness disturbance caused by omeprazole administration. A case report and literature review.

Digestive diseases and sciences·1996
Same author

Shared amino acid motifs in T-cell receptor beta junctional regions of bronchoalveolar T cells in patients with pulmonary sarcoidosis.

American journal of respiratory and critical care medicine·1996
Same author

Chloride transport across kidney epithelia through CLC chloride channels.

Nihon Jinzo Gakkai shi·1996
Same author

Specific binding sites for proadrenomedullin N-terminal 20 peptide (PAMP) in the rat.

Endocrinology·1996
Same author

Fibrinogen, coagulation factor VII, tissue plasminogen activator, plasminogen activator inhibitor-1, and lipid as cardiovascular risk factors in chronic hemodialysis and continuous ambulatory peritoneal dialysis patients.

American journal of kidney diseases : the official journal of the National Kidney Foundation·1996
Same author

Mild hypoxia induces hypertrophy of cultured neonatal rat cardiomyocytes: a possible endogenous endothelin-1-mediated mechanism.

Journal of molecular and cellular cardiology·1996
Same journal

[Development of novel therapeutics for multiple myeloma and improvement of drug lag].

Nihon rinsho. Japanese journal of clinical medicine·2019
Same journal

[Clinical pharmacy services to patients of immunomodulatory drugs].

Nihon rinsho. Japanese journal of clinical medicine·2019
Same journal

[Therapeutic drug monitoring of the new anti-myeloma drugs in the treatment of multiple myeloma].

Nihon rinsho. Japanese journal of clinical medicine·2019
Same journal

[Prognostic value of minimal residual disease assessment using next-generation sequencing in multiple myeloma].

Nihon rinsho. Japanese journal of clinical medicine·2019
Same journal

[The evaluation of minimal residual disease in multiple myeloma by an allele-specific oligonucleotide real-time PCR].

Nihon rinsho. Japanese journal of clinical medicine·2019
Same journal

[Evaluation of minimal residual disease in myeloma by multiparametric flow cytometry].

Nihon rinsho. Japanese journal of clinical medicine·2019
See all related articles

Endothelin-1 and nitric oxide (NO) are synthesized in the kidney, influencing renal function. Their receptors and related signaling molecules are present in various kidney structures, suggesting roles in modulating kidney function.

Area of Science:

  • Nephrology
  • Molecular Biology
  • Physiology

Background:

  • Endothelin-1 (ET-1) is synthesized in the kidney and affects renal function.
  • Endothelium-derived relaxing factor (EDRF) is nitric oxide (NO), synthesized from L-arginine by NO synthase.
  • NO stimulates soluble guanylate cyclase, increasing cyclic guanosine monophosphate (cGMP) levels.

Purpose of the Study:

  • To investigate the localization of Endothelin-1 (ET-1) and its receptors (ETA and ETB) in the kidney.
  • To examine the distribution of nitric oxide (NO) synthase and soluble guanylate cyclase mRNA in renal tissues.
  • To understand the potential roles of the ET-1 and NO/cGMP systems in modulating renal function.

Main Methods:

  • Reverse transcription polymerase chain reaction (RT-PCR) was used to detect mRNA expression.

Related Experiment Videos

  • Localization of ET-1 mRNA, ETA receptor mRNA, ETB receptor mRNA, NO synthase mRNA, and soluble guanylate cyclase mRNA was analyzed.
  • Main Results:

    • ET-1 mRNA was found in glomeruli and inner medullary collecting ducts.
    • ETA receptor mRNA was detected in glomeruli, vasa recta, and arcuate arteries.
    • ETB receptor mRNA was mainly distributed in glomeruli and collecting ducts.
    • NO synthase mRNA was present in glomeruli and inner medulla.
    • Soluble guanylate cyclase mRNA was widely distributed along nephron segments.

    Conclusions:

    • The ET-1 system components are present in specific renal structures, suggesting localized functions.
    • The NO/cGMP system is widely distributed within the nephron, indicating a broad role in renal physiology.
    • Both ET-1 and NO/cGMP systems likely play significant roles in modulating kidney function.