Related Experiment Video
Updated: Jul 14, 2026

05:48
An In Vivo Method to Study Mouse Blood-Testis Barrier Integrity
Published on: December 2, 2018
Drugs and the blood-testis barrier
Environmental Health Perspectives
|June 1, 1978
Summary
The blood-testis barrier controls substance entry into seminiferous tubules. Dimethylnitrosamine (DMNA) rapidly enters tubules, possibly after conversion from a precursor, concentrating toxins within.
Area of Science:
- Reproductive biology
- Toxicology
- Cellular physiology
Background:
- The blood-testis barrier (BTB) is crucial for maintaining the testicular microenvironment.
- Understanding how substances cross the BTB is vital for assessing testicular toxicity.
- Simple and facilitated diffusion are known mechanisms for substance transport across the BTB.
Purpose of the Study:
- To discuss evidence for the functional and morphological aspects of the blood-testis barrier.
- To examine the transport mechanisms of substances entering the seminiferous tubule.
- To investigate the differential entry rates of methylmethanesulfonate (MMS) and dimethylnitrosamine (DMNA) into the seminiferous tubules.
Main Methods:
- Review of functional and morphological evidence for the blood-testis barrier.
- Analysis of data on the entry of MMS and DMNA into seminiferous tubules.
- Comparison of observed entry rates with expected rates based on testicular DNA methylation.
Main Results:
- Both MMS and DMNA rapidly enter the seminiferous tubules.
- The rapid entry of DMNA contradicts expectations based on testicular DNA methylation rates.
- DMNA in blood appears to be gradually converted into a nonpermeant compound.
Conclusions:
- The blood-testis barrier permits rapid entry of both MMS and DMNA.
- DMNA's transport kinetics suggest a metabolic conversion in the blood prior to or during entry.
- A hypothesis is proposed for a precursor-mediated concentration of toxic substances within the tubules.
Related Concept Videos
Physiological Barriers
Physiological barriers are semi-permeable cellular structures restricting drug diffusion into intracellular compartments and tissues. There are six types of physiological barriers: blood endothelial, cell membrane, blood-brain, blood-cerebrospinal fluid (CSF), blood-placenta, and blood-testis barriers.
The blood endothelial barrier is the most porous of these. It allows all small ionized, un-ionized, and lipophilic molecules to pass through the endothelial lining into the interstitial space...
The blood endothelial barrier is the most porous of these. It allows all small ionized, un-ionized, and lipophilic molecules to pass through the endothelial lining into the interstitial space...
Factors Affecting Drug Distribution: Physiological Barriers
Drug distribution in the body is intricately regulated by various physiological barriers that control the passage of substances. These include the capillary endothelial barrier, the blood-brain, blood-cerebrospinal fluid, blood-placental, and blood-testis barriers.
The capillary endothelial barrier allows only smaller molecules below 600 Da (Daltons) to pass through. It also restricts drugs like heparin that are bound to blood components, limiting their movement within the bloodstream.
The...
The capillary endothelial barrier allows only smaller molecules below 600 Da (Daltons) to pass through. It also restricts drugs like heparin that are bound to blood components, limiting their movement within the bloodstream.
The...
Drug Binding to Blood Components
When drugs enter systemic circulation, they interact with various components of the blood, including proteins such as human serum albumin (HSA), α1-acid glycoprotein (AAG), lipoproteins, globulins, and red blood cells (RBCs).
HSA is the most abundant plasma protein and is vital in drug binding. It contains distinct drug-binding sites, with different drugs exhibiting affinity for specific sites. There are three main drug-binding domains for HSA: sites I, II, and III. These domains are further...
HSA is the most abundant plasma protein and is vital in drug binding. It contains distinct drug-binding sites, with different drugs exhibiting affinity for specific sites. There are three main drug-binding domains for HSA: sites I, II, and III. These domains are further...
Drug Elimination by Renal Route: Tubular Secretion
Once the process of glomerular filtration is completed, blood carrying unfiltered drug molecules traverses through efferent arterioles and makes its way into the peritubular capillaries in the proximal tubule. A variety of carriers play a pivotal role in actively secreting drugs from these peritubular capillaries into the tubular fluid. The organic anion transporter transfers acidic drugs, against an electrochemical gradient, from the peritubular capillaries into the renal tubule cells and...
Tissue-Drug Binding: Localization of Drugs and its Significance
Body tissues, comprising approximately 40% of the body weight, are crucial in drug distribution and localization. These tissues can serve as drug storage sites, competing with plasma binding sites for drug molecules.
Drugs can bind to different tissue components, enhancing their distribution and localization. The factors influencing drug localization in tissues include the drug's lipophilicity, structural characteristics, tissue perfusion rate, and pH differences. These factors determine the...
Drugs can bind to different tissue components, enhancing their distribution and localization. The factors influencing drug localization in tissues include the drug's lipophilicity, structural characteristics, tissue perfusion rate, and pH differences. These factors determine the...
The Blood-brain Barrier
Overview

