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- Clinical Physiology of the Kidneys
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1. Molecular basis of genetic renal diseases 1
- Dr. Paul Jennings
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2. Molecular basis of genetic renal diseases 2
- Dr. Paul Jennings
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3. Assessment of renal function
- Dr. Jochen Raimann
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4. Isolated microhematuria and proteinuria in adults
- Dr. Eva Seiringer
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5. Intradialytic oxygen saturation
- Dr. Lili Chan
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6. Pervasive sensing in chronic kidney disease
- Ms. Maggie Han
- Ms. Schantel Williams
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7. The genetic basis of kidney cancer
- Dr. W. Marston Linehan
- Glomerular Disorders
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8. Focal segmental glomerulosclerosis
- Prof. Moin Saleem
- Tubular Interstitial Disorders
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9. What’s new for IgA nephropathy part 1: epidemiology and pathogenesis
- Prof. Maurizio Salvadori
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10. What’s new for IgA nephropathy part 2: clinical presentation, diagnosis, prognosis, treatment
- Prof. Maurizio Salvadori
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11. Renal complications of sickle cell disease
- Dr. Claire Sharpe
- Acute Kidney Injury
- Chronic Kidney Disease
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13. Pathophysiology of acute renal failure
- Dr. Viviane Calice-Silva
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14. Anaemia in chronic kidney disease
- Prof. Iain Macdougall
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15. Kidney disease and pregnancy: a new era?
- Dr. Kate Bramham
- Renal Cell Carcinoma
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16. The genetics and genomics of familial renal carcinoma
- Prof. Eamonn Maher
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17. Immune checkpoint blockade in renal cell carcinoma
- Prof. David McDermott
- Pharmacology and the Kidney
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19. Toxicology of the kidney
- Prof. Lawrence Lash
- Proteomics and the Kidney
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20. Proteomics in diabetic kidney disease
- Prof. Peter Rossing
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21. Urinary proteomics in kidney and cardiovascular disease
- Prof. Harald Mischak
- Pediatric Nephrology
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22. Continuous renal replacement therapy (CRRT) in children
- Prof. Timothy E. Bunchman
- Archived Lectures *These may not cover the latest advances in the field
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23. Proteomics in kidney disease: clinical considerations
- Prof. Peter Rossing
Printable Handouts
Navigable Slide Index
- Introduction
- Lecture outline
- Renal structure
- Nephron heterogeneity
- Renal functions
- Filtration and reabsorption of electrolytes, water
- Susceptibility of the kidney to toxicant injury
- Renal blood flow
- Renal concentrating mechanisms
- Filtration, absorption, excretion
- Basic renal transport mechanisms
- Organic anion and cation transport processes
- Role of kidneys in fluid balance
- Bioactivation
- In vivo assessment of renal function
- Determination of GFR
- Relationships between SCr, BUN and GFR
- Parameters determined in typical urinalysis
- Proteinuria
- Enzymuria
- In vitro models for kidney toxicology
- In vitro models - isolated perfused kidney
- In vitro models - renal slices
- In vitro models - isolated perfused tubules
- In vitro models - isolated tubules/tubular fragments
- Models: suspensions of freshly isolated renal cells
- In vitro models - primary renal cell cultures
- In vitro models - renal cell culture lines
- Selected immortalized, continuous renal cell lines
- Acute renal failure
- Chronic renal failure
- Response to a nephrotoxicant
- Mechanisms of renal cell injury
- Nephron segment-specificity of nephrotoxicants
- Cadmium
- Cisplatin
- Halocarbon cysteine conjugates
- Trichloroethylene metabolism
- DCVC mechanisms of toxicity
- GSH and S-conjugate transport
- Structures of beta-lactam antibiotics
- Accumulation of beta-lactam in renal PT cells
- Mechanisms of toxicity of cephaloridine
- Bioactivation of acetaminophen
- References
- Acknowledgments
Topics Covered
- Renal structure and functions
- Renal blood flow
- Renal concentrating and transport mechanisms
- Role of kidneys in fluid balance
- In vivo assessment of renal function
- In vitro models to study kidney toxicology
- Classification of nephrotoxic injury
- Mechanisms of renal cell injury
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Lash, L. (2015, April 30). Toxicology of the kidney [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 1, 2024, from https://doi.org/10.69645/QUHX8060.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Lawrence Lash has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Pharmaceutical Sciences
Transcript
Please wait while the transcript is being prepared...
0:00
This is Lawrence Lash. I'm a professor in the Department of Pharmacology
at Wayne State University School of Medicine in Detroit, Michigan,
and the topic of my talk will be the Toxicology of the Kidney.
0:15
As you can see on this slide, there will be five major sections to the talk.
The first section, I will review a few key points about renal structure and physiology
that are important in terms of understanding why the kidney
is susceptible to toxic injury and what is unique about renal structure and function.
In the second section we will specifically address factors that are important
in determining susceptibility of the kidney to toxicant injury.
In the third and fourth sections, I will talk about different models,
first in vivo models and then various in vitro models,
that are used to discuss and study toxicology of the kidney,
and then finally as some illustrations of how chemicals can produce toxicity
in the kidney and some of the unique features as case studies,
we will review briefly some examples: heavy metals,
cadmium and mercury principally; halogenated solvents; antibiotics;
and finally analgesics.
1:30
This slide illustrates some aspects of renal structure. First there's a nephron
that is a deep nephron that goes all the way into the inner medulla
as well as a superficial nephron on the right, which only goes to the outer stripe
inner medulla border. The slide illustrates the different major epithelial cell types
beginning with the glomerulus. This is number one.
This leads into the proximal tubules, which is number two,
first the proximal convoluted tubule in the cortex, then in the cortex
and outer stripe of the outer medulla, one has the proximal straight tubule,
then flows into the thin descending limb, then thick ascending limb, and finally
into the distal tubule, connecting tubule, and into the collecting duct.
And the importance of understanding this is that each cell type,
each epithelial cell type, has a specific structure and function
that, while allowing the kidney to have its unique physiology
also provides some unique features to the susceptibility to chemically-induced injury.