Effect of Drakshavaleha in cyclophosphamide induced weight loss and reduction in crown-rump length in developing mice

Sunil Kumar1, Gajendra Singh, K R C Reddy

  • 1Associate Professor Department of Sharira Rachana , National Institute of Ayurveda, Jaipur, India.

Ayu
|November 20, 2013
PubMed

Insights

Cyclophosphamide (CP) causes growth stunting in pups. Supplementing pregnant mice with Drakshavaleha significantly minimized this weight loss and improved pup size, indicating a protective effect.

Area of Science:

  • Reproductive toxicology
  • Developmental biology
  • Pharmacology

Background:

  • Cyclophosphamide (CP) is an anti-mitotic and apoptosis-inducing agent.
  • CP administration during gestation can lead to adverse fetal outcomes, including growth retardation.
  • Herbal formulations are explored for mitigating drug-induced developmental toxicity.

Purpose of the Study:

  • To investigate the protective effects of Drakshavaleha against Cyclophosphamide-induced developmental toxicity in mice.
  • To evaluate the impact of Drakshavaleha on fetal growth parameters compromised by CP exposure.

Main Methods:

  • Pregnant mice were administered Cyclophosphamide (10 mg/kg) intraperitoneally on day 11 of gestation.
  • A separate group received Drakshavaleha (16 g/kg) orally from day 0 to day 18 of gestation.
  • Fetal parameters including body weight and crown-rump length were assessed and compared to control groups.

Main Results:

  • Cyclophosphamide administration resulted in significant stunting of pup size and reduced body weight.
  • Oral administration of Drakshavaleha significantly minimized the body weight loss induced by CP (P < 0.001).
  • Drakshavaleha treatment also led to the recovery of crown-rump length in pups exposed to CP.

Conclusions:

  • Drakshavaleha exhibits a protective effect against Cyclophosphamide-induced fetal growth retardation.
  • This herbal supplement can mitigate adverse developmental outcomes associated with CP exposure during pregnancy.
  • Drakshavaleha shows potential as an adjunct therapy to reduce CP-related teratogenicity.

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