<b>PHARMACOLOGICAL EVALUATION OF </b><b>Silybum marianum </b><b>(L.) SEED</b><b> </b><b>EXTRACT: ANALGESIC, ANTI-INFLAMMATORY, DIURETIC, AND</b><b> </b><b>ANTIDIARRHEAL ACT

Silybum marianum (milk thistle) seeds contain a flavonoid-rich extract that has been used for liver disorders. However, it has not been extensively studied for its analgesic, anti-inflammatory, diuretic, and antidiarrheal properties. We tested an ethanolic seed extract (SME) in standard rodent models. Swiss albino mice and Wistar rats (n=8) were divided into three groups: control, standard drug, and SME-treated (100, 200, 400 mg/kg p.o.). Sample sizes were determined using power analysis (α=0.05, β=0.2) based on preliminary variability. The study evaluated analgesic activity through acetic acid writhing (visceral pain) and tail-flick (thermal nociception), as well as anti-inflammatory activity through carrageenan-induced paw edema, diuretic activity through 24-hour urine output and electrolyte excretion (versus furosemide), and antidiarrheal activity through castor oil-induced diarrhea (versus loperamide). The extract significantly reduced writhing counts (73% inhibition at 400 mg/kg, p<0.01) and prolonged tail-flick latency, comparable to aspirin. Carrageenan-induced paw edema was dose-dependently suppressed, with 46% inhibition at 400 mg/kg (vs. 48% by aspirin) at 4 hours (p<0.01). SME showed moderate increases in urine volume (96% at 400 mg/kg, p<0.05) and natriuresis, but not as much as furosemide (156% increase, p<0.001). In the antidiarrheal test, the extract delayed diarrhea onset and decreased fecal output (70% reduction at 400 mg/kg, p<0.01). There was no overt toxicity observed. Phytochemical profiling (HPLC) revealed that SME contains silibinin (~60%), silychristin (~10%), silydianin (~10%), isosilybins (~5%), and taxifolin (~5%) [6,17]. S. marianum seed extract has analgesic, anti- inflammatory, mild diuretic, and antidiarrheal properties. The flavonoid composition correlates with the multi-modal bioactivity. This preclinical profile suggests that S. marianum seeds could be used as a phytomedicine to treat pain, inflammation, and gastrointestinal disturbances, necessitating further mechanistic and clinical research.

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Journal
Journal of medical & health sciences review.
Published
2025-09-04
DOI
https://doi.org/10.62019/v04bgr93
Primary Topic
Silymarin and Mushroom Poisoning
Type
article
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article

PHARMACOLOGICAL EVALUATION OF Silybum marianum (L.) SEED EXTRACT: ANALGESIC, ANTI-INFLAMMATORY, DIURETIC, AND ANTIDIARRHEAL ACT

Slim Ben Ahmed, Saira Shah, Safia Abidi, Sadia Ghousia Baig et al.
Journal of medical & health sciences review.
Silymarin and Mushroom Poisoning
article

PHARMACOLOGICAL EVALUATION OF Silybum marianum (L.) SEED EXTRACT: ANALGESIC, ANTI-INFLAMMATORY, DIURETIC, AND ANTIDIARRHEAL ACT

Slim Ben Ahmed, Saira Shah, Safia Abidi, Sadia Ghousia Baig, Umbreen Farrukh, Samreen Mujahid
article en

Abstract

Silybum marianum (milk thistle) seeds contain a flavonoid-rich extract that has been used for liver disorders. However, it has not been extensively studied for its analgesic, anti-inflammatory, diuretic, and antidiarrheal properties. We tested an ethanolic seed extract (SME) in standard rodent models. Swiss albino mice and Wistar rats (n=8) were divided into three groups: control, standard drug, and SME-treated (100, 200, 400 mg/kg p.o.). Sample sizes were determined using power analysis (α=0.05, β=0.2) based on preliminary variability. The study evaluated analgesic activity through acetic acid writhing (visceral pain) and tail-flick (thermal nociception), as well as anti-inflammatory activity through carrageenan-induced paw edema, diuretic activity through 24-hour urine output and electrolyte excretion (versus furosemide), and antidiarrheal activity through castor oil-induced diarrhea (versus loperamide). The extract significantly reduced writhing counts (73% inhibition at 400 mg/kg, p<0.01) and prolonged tail-flick latency, comparable to aspirin. Carrageenan-induced paw edema was dose-dependently suppressed, with 46% inhibition at 400 mg/kg (vs. 48% by aspirin) at 4 hours (p<0.01). SME showed moderate increases in urine volume (96% at 400 mg/kg, p<0.05) and natriuresis, but not as much as furosemide (156% increase, p<0.001). In the antidiarrheal test, the extract delayed diarrhea onset and decreased fecal output (70% reduction at 400 mg/kg, p<0.01). There was no overt toxicity observed. Phytochemical profiling (HPLC) revealed that SME contains silibinin (~60%), silychristin (~10%), silydianin (~10%), isosilybins (~5%), and taxifolin (~5%) [6,17]. S. marianum seed extract has analgesic, anti- inflammatory, mild diuretic, and antidiarrheal properties. The flavonoid composition correlates with the multi-modal bioactivity. This preclinical profile suggests that S. marianum seeds could be used as a phytomedicine to treat pain, inflammation, and gastrointestinal disturbances, necessitating further mechanistic and clinical research.

Journal of medical & health sciences review.Vol. 2(3)
University of Karachi (PK), Baqai Medical University (PK), Dow University of Health Sciences (PK), Pharmac (NZ)
Openalex Percentile: Top 65%
Silymarin and Mushroom Poisoning
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