Testicular Dysfunction

Testicular dysfunction refers to impaired testicular structure or function that disrupts hormone production, sperm development, or both, making it an important cause of male reproductive and endocrine disorders. It can arise when damage to testicular tissue, abnormal hormonal signaling, genetic conditions, infection, medications, or other disease interferes with testosterone synthesis or the coordinated stages of spermatogenesis. Clinical assessment may combine medical history, physical examination, hormone testing, semen analysis, and imaging to identify underlying abnormalities. Understanding these mechanisms supports diagnosis and treatment of infertility, hypogonadism, and related health problems, while informing research into reproductive medicine and long-term endocrine outcomes.

Testicular Dysfunction - Related Videos

Research

JoVE Journal - Biology

Simple and Efficient Technique for the Preparation of Testicular Cell Suspensions

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Cited by 20 •

2013

A novel protocol for the mechanical preparation of testicular cell suspensions from rodent material, avoiding enzymes and detergents, is described. The method is very simple, fast, reproducible, and renders good quality cell suspensions, which are suitable for flow sorting and RNA extraction.

Research

JoVE Journal - Neuroscience
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Mapping Dysfunctional Protein-Protein Interactions in Disease

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2025

Here, we present a protocol to enable the capture and identification of disease-specific protein-protein interactions from native cells and tissues using chemical probes and mass spectrometry. The resulting interaction datasets are analyzed through a dedicated web-based platform to reveal dynamic network dysfunctions and pathway alterations linked to disease.

Mouse Model of Metabolic Dysfunction-Associated Steatotic Liver Disease with Fibrosis

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Cited by 1 •

2025

Mouse model of metabolic dysfunction-associated steatotic liver disease (MASLD) with metabolic dysfunction, hepatic gene expression changes, and liver histopathological alterations that resemble human MASLD, including fibrosis that progresses to advanced fibrosis stage 3. This model can be used in studies of MASLD pathophysiology and in pre-clinical studies of new therapies.

Slide Preparation Method to Preserve Three-dimensional Chromatin Architecture of Testicular Germ Cells

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Cited by 12 •

2014

The material here describes a method developed to preserve the three-dimensional chromatin structure of testicular germ cells. This has been termed the three-dimensional (3D) slide method. This method improves sensitivity for detection of subnuclear structures and is applicable for immunofluorescence, DNA, and RNA fluorescence in situ hybridization (FISH).

Research

JoVE Journal - Medicine
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Early Detection of Drug-Induced Renal Hemodynamic Dysfunction Using Sonographic Technology in Rats

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Cited by 14 •

2016

Early stage hemodynamic dysfunction is critical to the development of kidney disease. Yet, detection methodologies are limited. Recent advances in sonography provide a noninvasive, accurate option for early detection of kidney injury. This study outlines a step-by-step, sonographic methodology for detecting kidney dysfunction using a drug-induced nephrotoxicity rat model.

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