𝔖 Bobbio Scriptorium
✦   LIBER   ✦

rhGGF2 protects against cisplatin-induced neuropathy in the rat

✍ Scribed by Mariël P. ter Laak; Frank P.T. Hamers; Cassandra J. Kirk; Willem Hendrik Gispen


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
199 KB
Volume
60
Category
Article
ISSN
0360-4012

No coin nor oath required. For personal study only.

✦ Synopsis


In many patients treated with cisplatin a peripheral sensory neuropathy develops. This side-effect is considered dose-limiting, and therefore restricts the total dose of cisplatin that can be administered. Recent in vitro and in vivo studies suggest that recombinant human Glial Growth Factor 2 (rhGGF2) has neuroprotective effects. This prompted us to investigate in a rat model whether rhGGF2 ameliorates cisplatin neuropathy. A total of 48 rats were randomly divided into four groups of 12 rats each. Three groups received cisplatin and were treated with either 0.1 mg/kg rhGGF2, 0.3 mg/kg rhGGF2 or placebo. The fourth group (saline/placebo) served as age-matched controls. In the cisplatin/placebo treated rats a neuropathy developed, as determined by measurements of the nerve conduction velocity (NCV). Treatment with rhGGF2 dose-dependently protected against the neuropathy. Histological examination and morphometric analysis revealed that rhGGF2 also protects against cisplatin-induced changes in the morphology and size of DRG satellite cell nuclei. In a control study rhGGF2 did not affect normal NCV development. We conclude that rhGGF2 treatment is of benefit in the treatment of cisplatin neuropathy in the rat.


📜 SIMILAR VOLUMES


Protective Effects of Methimazole agains
✍ Helmut Bräunlich; Dorothea Appenroth; Christian Fleck 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 159 KB 👁 2 views

Key words: nephrotoxicity; cisplatin; radical scavengers; methimazole; rat In adult rats 6 mg kg -1 body wt. cisplatin given i.p. was nephrotoxic. Four days of i.p. treatment with 40 mg kg -1 body wt. methimazole, which started 1 day before CP, prevented increases in blood urea nitrogen and in the r

Taurohyodeoxycholic acid protects agains
✍ Aldo Roda; Francesco Piazza; Mario Baraldini; Ester Speroni; Maria Clelia Guerra 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 106 KB

The prevention of the hepatotoxic effects produced by intravenous infusion of taurochenodeoxycholic acid (TCDCA) by coinfusion with taurohyodeoxycholic acid (THDCA) was evaluated in bile fistula rats; the hepatoprotective effects of the latter were also compared with those of tauroursodeoxycholic ac

Melatonin protects against taurolithocho
✍ Lorena Fuentes-Broto; Francisco J. Miana-Mena; Eduardo Piedrafita; César Berzosa 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 215 KB 👁 1 views

## Abstract Cholestasis, encountered in a variety of clinical disorders, is characterized by intracellular accumulation of toxic bile acids in the liver. Furthermore, oxidative stress plays an important role in the pathogenesis of bile acids. Taurolithocholic acid (TLC) was revealed in previous stu

The protective effect of N-acetylcystein
✍ Hasan Kaya; Ahmet Koc; Sadik Sogut; Mehmet Duru; H. Ramazan Yilmaz; Efkan Uz; Ra 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 223 KB 👁 1 views

## Abstract The immunosuppressive agent cyclosporine A (CsA) has been reported to exert measurable hepatotoxic effects. One of the causes leading to hepatotoxicity is thought to be reactive oxygen radical formation. The aim of this study was to investigate the effects of __N__‐acetylcysteine (NAC)

16,16-Dimethyl-PGE2 Protection Against α
✍ Mary J. Ruwart; Bob D. Rush; Nanette M. Friedle; Jerzy Stachura; Andrzej Tarnaws 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 340 KB

Male rats were treated with subcutaneous vehicle or 16,16-dimethyl-PGEz (dmPGEn, 100 pg per kg), 24,18 and 0.6 hr prior to and 6 , 2 4 and 30 hr after challenge with oral a-napthylisothiocyanate (ANIT, 30 mg per kg). Forty-eight hours after challenge, rats were sacrificed by decapitation; serum and