Qualitative and Quantitative Analysis of the Effects of Quinazolinones on Internal Organs of Newborn Balb/C Mice

سال انتشار: 1388
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 160

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شناسه ملی سند علمی:

JR_IJBMS-12-2_008

تاریخ نمایه سازی: 30 مهر 1400

چکیده مقاله:

Objective(s) Quinazolinones are heterocyclic compounds, with biological and pharmacological activities, such as inhibiting some proteins, enzymes and reducing blood lipids. Materials and Methods Following previous results of our group, effects of two new derivatives of quinazolinones ۹(۳)-quinazolinone-۲-propyl-۲-phenylethyl (QPPE) and ۹(۳)-quinazolinone-۲-ethyl-۲-phenylethyl (QEPE) on livers, intestines and kidneys of newborn Balb/C mice were investigated. Pregnant mice were divided into four groups of control, sham, experimental ۱, treated with QPPE, and experimental ۲, treated with QEPE. Experimental groups received ۱۰۰ mg/kg body weight (most effective dose) of QPPE and QEPE, sham groups received methyl cellulose ۰.۰۵% (the solvent) and control groups received distilled water, intraperitoneally (IP), on day ۸ of gestation. Five days after birth, livers, intestines and kidneys were removed, fixed in formalin ۱۰%, stained with hematoxylene and eosin for histological and pathological studies. Results Results showed appearance of fatty changes in livers, an increase in diameters of hepatocytes and central veins of livers, and reduction in the lengths of villi of proximal, middle and distal segments of newborn Balb/C mice intestines. Furthermore, there was a diminished diameter of the lumen of the proximal tubules, and average diameter of the lumen of distal tubules which led to an increase in the number of glomeruli cells of newborn Balb/C mice kidneys. Conclusion Regarding inflammation in different parts of the kidneys, livers and intestines, our investigations suggest that quinazolinones may have some toxic effects on embryos.

نویسندگان

Maryam Shams Lahijani

Developmental Biology,Animal Sciences, Faculty of Biological Sciences, Shahid-Beheshti University (SBU),G.C., Tehran, Iran

Hoda Rajabi

Developmental Biology,Animal Sciences, Faculty of Biological Sciences, Shahid-Beheshti University (SBU),G.C., Tehran, Iran

Samar Etemad

Developmental Biology,Animal Sciences, Faculty of Biological Sciences, Shahid-Beheshti University (SBU),G.C., Tehran, Iran

Mahla Fadavi Eslam

Developmental Biology,Animal Sciences, Faculty of Biological Sciences, Shahid-Beheshti University (SBU),G.C., Tehran, Iran

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  • ۱.Fawzia MR, Amr YE, Soad M, Aida MI, Mona AM. ...
  • ۲.Vuong NT, Xing-Ping L, Chun-Lin C, Fatih MU. Treatment of ...
  • ۳.Shams Lahijani M, Aounegh R. Teratogenic effects of quinazolinones on ...
  • ۴.Shams Lahijani M, Ahmanzadeh F, Dabiri M. Teratogenic effects of ...
  • ۵.Etemad S, Shams Lahijani M. Quinazolinones and nerphrotoxicity in new ...
  • ۶.Rajabi H, Shams Lahijani M. Histological study of liver of ...
  • ۷.Etemad S, Shams Lahijani M. Studying quinazolinones derivatives treatments as ...
  • ۹.Etemad S, Shams Lahijani M. Pathological effects of quinazolinones on ...
  • ۱۰.Dabiri M, Salehi P, Khajavi MS, Mohammadi A. Microwae-assisted one-pot ...
  • ۱۱.Placidi GF, Fornaro P, Guarneri M. Autoradiographic distribution study of ...
  • ۱۲.Maggio B, Daidone G, Raffa D, Plescia S, Mantione L, ...
  • ۱۳.Condino AA, Barleycorn AA, Lu W, Maheshwari A, Christensen RD, ...
  • ۱۴.Morgan MY, Reshef R, Shah RR, Oates NS, Smith RL, ...
  • ۱۵.Pessayre D. Role of reactive metabolites in drug-induced hepatitis. J ...
  • ۱۶.Arici M, Chana R, Lewington A, Brown J, Brunskill NJ. ...
  • ۱۷.Tzen CY, Tsai JD,Wu TY,Chen BF, Chen ML, Lin SP, ...
  • ۱۸.Recknagel RO, Glende EA Jr. Carbon tetrachloride hepatotoxicity: an example ...
  • ۱۹.Raffa D, Elder MC, Daidone G, Maggio B, Merickech M, ...
  • ۲۰.Fledman M, Friedman LS, Sleisenger MH. Anatomy/histology/embryology/and developmental anomalies of ...
  • ۲۱.Woolf AS, Hillman KA. Unilateral renal agenesis and the congenital ...
  • ۲۲.Moritz KM, Dodie M, Wintour M. Kidney development and the ...
  • ۲۳.Shimizu A, Masuda Y, Kitamura H, Ishizaki M, Sugisaki Y,Yamanaka ...
  • ۲۴.Jenette JC, Thomas DB. Crescentic glomerulonephritis.Nephrology Dial Transplant ۲۰۰۱; ۱۶:۸۰-۸۲ ...
  • ۲۵.Dixon JL, Ginsberg HN. Hepatic synthesis of lipoproteins and apolipoproteins. ...
  • ۲۶.Muriel P, Mourelle M. Prevention by silymarin of membrane alterations ...
  • ۲۷.Masayasu I, Sato EF, Nishikawa M, Park AM, Kira Y, ...
  • ۲۸.Horikoshi S, Tomino Y. Tubulointerstitial nephropathy in mitochondrial cytopathy. Nippon ...
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