Insights Into the Molecular Mechanisms of Polycystic Kidney Diseases

Valeriia Y Vasileva1, Regina F Sultanova2,3, Anastasia V Sudarikova1

  • 1Institute of Cytology, Russian Academy of Sciences, St. Petersburg, Russia.

Frontiers in Physiology
|September 27, 2021
PubMed

Insights

Polycystic kidney disease (PKD) involves kidney cyst growth, leading to renal failure. This review explores PKD mechanisms and potential non-drug therapies like diet to manage the condition.

Area of Science:

  • Nephrology
  • Genetics
  • Molecular Biology

Background:

  • Autosomal dominant (AD) and autosomal recessive (AR) polycystic kidney diseases (PKD) are severe genetic disorders causing kidney cyst formation and renal function loss.
  • Current treatments are limited; tolvaptan offers modest ADPKD symptom relief but has side effects and doesn't halt progression.

Purpose of the Study:

  • To review fundamental mechanisms driving PKD development, focusing on ADPKD.
  • To explore molecular cascades, systemic responses, and non-pharmacological therapies for PKD.

Main Methods:

  • Literature review of current knowledge on PKD pathogenesis.
  • Analysis of PC1/PC2 pathways, cilia-associated mechanisms, metabolism, mitochondrial function, and systemic factors.
  • Examination of non-pharmacological interventions, including dietary approaches.

Main Results:

  • Highlights key pathways (PC1/PC2, cilia) and molecular cascades (metabolism, mitochondria) implicated in PKD.
  • Discusses systemic influences: hormonal status, growth factors, immune system, and microbiome.
  • Reviews emerging non-pharmacological therapies, such as dietary interventions.

Conclusions:

  • A deeper understanding of PKD mechanisms is crucial for developing effective treatments.
  • Non-pharmacological strategies, particularly dietary modifications, show promise for alleviating PKD symptoms and progression.

Related Concept Videos

Chronic Kidney Disease I: Introduction01:25

Chronic Kidney Disease I: Introduction

Chronic Kidney Disease (CKD) arises when the kidneys progressively lose their ability to function, ultimately leading to end-stage renal disease. At this advanced stage, the kidneys can no longer filter waste or maintain essential body functions, requiring renal replacement therapy (RRT) through dialysis or a kidney transplant for survival.Early-stage chronic kidney disease and detection challengesIn CKD's early stages, symptoms often remain absent because healthy nephrons compensate for...
192
Nephrons01:10

Nephrons

The kidneys are intricate organs with millions of working units known as nephrons. Each nephron features two major structures: the renal corpuscle, which facilitates blood plasma filtration, and the renal tubule, which handles the glomerular filtrate. Blood supply is directly linked to the nephrons. The renal corpuscle consists of the glomerulus, a capillary network, and the Bowman's capsule, a double-walled epithelial structure that encases the glomerulus. The filtering of blood plasma...
3.9K
Renal Corpuscle01:20

Renal Corpuscle

The glomerulus and Bowman's capsule are two essential components of the nephron, which is the functional unit of the kidney. These microscopic structures play a critical role in the process of blood filtration to produce urine.
Glomerulus: Structure and Function
The glomerulus is a tiny, intricate network of capillaries located at the beginning of the nephron. It's enveloped by the Bowman's capsule and receives its blood supply from an afferent arteriole, which divides into numerous...
3.9K
Renal Tubule and Collecting Duct01:24

Renal Tubule and Collecting Duct

The renal tubule is divided into three parts: the proximal convoluted tubule (PCT), the Loop of Henle (LOH), and the distal convoluted tubule (DCT).
Proximal Convoluted Tubule (PCT):
The PCT is the initial segment of the renal tubule, extending from the Bowman's capsule that encloses the glomerulus. Its convoluted structure and microvilli-lined cells increase the surface area for reabsorption. The PCT reabsorbs glucose, amino acids, sodium, and water from the filtrate, ensuring essential...
1.8K
Cystic Fibrosis: Pathogenesis01:23

Cystic Fibrosis: Pathogenesis

Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
424
Chronic Kidney Disease II: Clinical Manifestations01:24

Chronic Kidney Disease II: Clinical Manifestations

Chronic Kidney Disease (CKD) progressively impairs multiple body systems due to the accumulation of uremic toxins, which disrupt cellular functions across various organs.Neurologic symptomsNeurologic symptoms often arise early in CKD, as uremic toxin buildup drives changes in cognitive and motor functions. Patients frequently experience fatigue, headache, confusion, difficulty concentrating, and, in severe cases, seizures. Peripheral neuropathy commonly manifests as burning sensations in the...
164