Evaluation of the anti-inflammatory activity of N,N '-bis(3-dimethylamino-1-phenyl-propylidene) hydrazine dihydrochloride


GÜL H. İ., Suleyman H., GÜL M.

PHARMACEUTICAL BIOLOGY, cilt.47, sa.10, ss.968-972, 2009 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 47 Sayı: 10
  • Basım Tarihi: 2009
  • Doi Numarası: 10.1080/13880200902967961
  • Dergi Adı: PHARMACEUTICAL BIOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.968-972
  • Atatürk Üniversitesi Adresli: Evet

Özet

This study investigated the anti-inflammatory effect of N, N'-bis(3-dimethylamino-1-phenyl-propylidene) hydrazine dihydrochloride, D1, on carrageenan-induced edema. In addition, its effect on hyaluronidase-induced vascular permeability was also tested. D1 was synthesized, and anti-inflammatory activity was determined by carrageenan-induced hind paw edema in rats (n = 30) at 50, 100, and 200 mg kg(-1) doses of D1 and also a 25 mg kg(-1) dose of indomethacin. The effects of D1 and indomethacin on hyaluronidase-induced capillary permeability were investigated in rabbits (n = 18) at a 100 mg kg(-1) dose of D1 and 25 mg kg(-1) dose of indomethacin. D1 inhibited carrageenan-induced inflammation by 40, 20, and 10% at 50, 100, and 200 mg kg(-1) doses after 1 h. The inhibitions were 22.5, 32.7, 28.6% and 15.6, 33.4, 8.9% at 2 h and 3 h, respectively. The inhibitions due to indomethacin (25 mg kg(-1) dose) were 67.5, 87.8, and 91.1%, at 1 h, 2 h, and 3 h, respectively. The subcutaneous spreading areas of Trypan blue at 1, 5, 30, and 60 min after subcutaneous injection of hyaluronidase were 172.6 +/- 41.6, 210.2 +/- 39.7, 363 50, and 400.2 +/- 46.7 mm(2) in the D1 (100 mg kg-1) treated group. The spreading areas at these time periods were 38.8 +/- 3.7, 48.2 +/- 4.5, 100.6 +/- 6.9, and 119.8 +/- 22.5 mm(2) in the indomethacin treated group. Our results showed that D1 inhibits carrageenan-induced inflammation in rats. A tendency to decrease the capillary permeability suggested that the mechanism of action of the anti-inflammatory effect of D1 may partly depend on inhibition of the hyaluronidase enzyme.