Morin hydrate mitigates calcium oxalate urolithiasis by inhibiting oxalate synthesis and modulating crystal formation

Mounica Ponugoti1,2, Chakravarthi Guntupalli3, Narender Malothu1

  • 1KL College of Pharmacy, Koneru Lakshmaiah Education Foundation, Vaddeswaram, Guntur, Andhra Pradesh, 522502, India.

Urolithiasis
|September 5, 2024
PubMed

Insights

Morin Hydrate shows promise in preventing calcium oxalate kidney stones by inhibiting oxalate production and crystal formation. This natural compound also exhibits diuretic effects and protects kidney tissue.

Area of Science:

  • Biochemistry
  • Pharmacology
  • Nephrology

Background:

  • Calcium oxalate (CaOx) urolithiasis is a common urinary stone disease.
  • Developing effective preventive therapies for CaOx stones is a significant clinical need.

Purpose of the Study:

  • To investigate the therapeutic potential of Morin Hydrate (MH), a natural bioflavonoid, in preventing CaOx urolithiasis.
  • To elucidate the mechanisms underlying MH's anti-urolithic effects.

Main Methods:

  • Molecular docking simulations to assess MH binding to glycolate oxidase (GO).
  • In vitro assays to evaluate MH's effect on CaOx crystal nucleation, aggregation, and growth.
  • In vivo studies in Wistar rats to assess diuretic activity and therapeutic efficacy in a urolithiasis model.
  • Biochemical analysis of urinary and serum markers, oxidative stress indicators, and renal tissue histopathology.

Main Results:

  • MH demonstrated strong binding to GO, suggesting inhibition of oxalate synthesis.
  • In vitro, MH inhibited CaOx crystal nucleation, aggregation, and growth, altering crystal morphology.
  • MH exhibited moderate diuretic activity, increasing urine volume and ion excretion.
  • In vivo, MH treatment improved renal function markers, reduced oxidative stress, protected renal tissue, and decreased GO and lactate dehydrogenase activities.

Conclusions:

  • Morin Hydrate is a promising natural compound for preventing and treating CaOx urolithiasis.
  • MH acts by inhibiting oxalate production, crystal formation, and exhibiting diuretic and renoprotective effects.
  • MH holds potential for clinical application in managing kidney stone risk and recurrence.

Related Concept Videos

Antihypertensive Drugs: Vasodilators01:23

Antihypertensive Drugs: Vasodilators

Vasodilators, primarily affecting the smooth muscles within arterial and venous walls, are commonly used for hypertension treatment. Medications such as minoxidil and hydralazine primarily target arteries and arterioles, while sodium nitroprusside acts on arterioles and venules. Minoxidil, functioning as a prodrug, is metabolized by hepatic sulfotransferase into its active form, minoxidil sulfate, after oral administration. This metabolite binds to the sulfonylurea receptor (SUR) component of...
492
Factors Affecting Solubility04:01

Factors Affecting Solubility

Compared with pure water, the solubility of an ionic compound is less in aqueous solutions containing a common ion (one also produced by dissolution of the ionic compound). This is an example of a phenomenon known as the common ion effect, which is a consequence of the law of mass action that may be explained using Le Chȃtelier’s principle. Consider the dissolution of silver iodide:
33.3K
Antihypertensive Drugs: Action of Calcium Channel Blockers01:18

Antihypertensive Drugs: Action of Calcium Channel Blockers

Calcium ions are essential to contract smooth muscle cells in blood vessels. They enter these cells through voltage-dependent calcium channels, specifically L-type calcium channels in the cell membrane. These L-type calcium channels are integral to the excitation-contraction coupling process in smooth muscle. When a stimulus is received by smooth muscle cells, their membrane depolarizes. This alteration in membrane potential instigates the opening of L-type calcium channels. As a result,...
473
Antihypertensive Drugs: Thiazide-Class Diuretics01:15

Antihypertensive Drugs: Thiazide-Class Diuretics

Thiazide diuretics are sulfonamide derivatives featuring a benzothiadiazine ring system in their molecular structure. Based on this structure, thiazide diuretics can be categorized into two groups: thiazide-type and thiazide-like diuretics. Thiazide-type diuretics, including hydrochlorothiazide and chlorothiazide, consist of a benzothiadiazine backbone with an attached sulfonamide group. Thiazide-like diuretics, such as chlorthalidone and indapamide, lack the thiazide ring but demonstrate...
563
Antihypertensive Drugs: Potassium-Sparing Diuretics01:28

Antihypertensive Drugs: Potassium-Sparing Diuretics

Liddle syndrome is a genetically inherited form of hypertension characterized by the overactivity of epithelial sodium channels in the nephron, the functional unit of the kidney. This heightened activity leads to increased sodium reabsorption and excessive excretion of potassium. To counteract this, potassium-sparing diuretics such as amiloride are used. They function by blocking these sodium channels, thereby reducing the influx of sodium into the epithelial cells and minimizing the loss of...
476
Antianginal Drugs: Calcium Channel Blockers and Ranolazine01:25

Antianginal Drugs: Calcium Channel Blockers and Ranolazine

Angina pectoris, a primary symptom of ischemic heart disease, requires careful pharmacological interventions. In this context, calcium channel blockers (CCBs) and ranolazine have emerged as crucial pharmacotherapeutic agents, providing deep insights into the complexities of angina management.
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...
464