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Exposure of Pregnant Mice to Hexavalent Chromium Causes Fetal Defects

Exposure of Pregnant Mice to Hexavalent Chromium Causes Fetal Defects

Madeeha Arshad1, Naveed Ahmad2,*, Muhammad Khalid3, Asmatullah1, Mohammad Tahir2, Khadija Naveed1 and Asia Iqbal4

1Department of Zoology, University of the Punjab, Quaid-i-Azam Campus, Lahore, Pakistan
2Department of Environment Sciences, COMSATS Institute of Information Technology, Vehari Campus, Vehari, Pakistan
3Department of Veterinary Clinical Sciences, The Royal Veterinary College, Hawkshead Lane, North Mymms, Hatfield, Hertfordshire, AL9 7TA, UK 
4University of Veterinary and Animal Sciences, Pattoki Campus, Pattoki, Pakistan 

*     Corresponding author: naveedahmad@ciitvehari.edu.pk

Fig 1

Morphological features of 18 days oldfetuses of mice administration with K2Cr2O7 at a dose of 22µg/g B.W. (A, B), and 11µg/g B.W. (C-G) Control, Vehicle control (VC); Df, deformed; Hd, hydrocephaly; Ls, laproschisis; Mg, macroglossia; R, resorption. DA, dilated abdomen; Ex, exencephaly; KT, kinked tail; Mc, Microcephaly; Om, Omphalocoel. Magnificaton: A=10X, B&D=25X, C, E&G=8X, F=9X

Fig 2

Morphological features of 18 days old fetuses of mice, administered with K2Cr2O7 at a dose of 44µg/g B.W. A, Control; B, VC, vehicle control; AO, anophthalmia; AT, abnormal tail; Cl, clinodactyly; DW, drooped wrist; Ex, exencephaly; FD, fused digits; Hm, hemorrhage; KT, kinked tail; MR, malrotation. Magnification: A=7X, B&C=8X, D=25X, E=20X, F=10X, F=9X.

Fig 3

Histological transverse sections of Control (A), Vehicle control (B) of different dose groups (44,22,11µg/g B.W) (C-H), 18 days old fetus from brain, Ex: exencephaly, M Vent: misshapen ventricle, HB: hind brain, MB, mandibular gland; FP, fused pinna, M sub corticle region: misshapen sub corticle region; Co, cortex; RA, right atrium; LA, left atrium; RA, right atrium; M Sc, misshapen spinal cord; SB, spina bifida; Om, Omphalocoel; NC, nasal cavity; Sg, serous gland; IRS, intra retinal space; RLV, right lateral ventricle, MB, mandibular gland; CA, cerebral aquaduct; LLV, left lateral ventricle; HC, hyaloid cavity; NS, nasal septum; FV, follicles of vibrissae; L, lens; FB, primordium of 1frontal bone; NLR, neural layer of retina; PM, pre molar.

Fig 4

Skeletons of control (A) and vehicle control (B), and selected sections from different dose groups (11,22,44µg/g B.W) (C-E). Simple arrows show less degree ossification while bold arrows show no ossification in three different dose groups. F, Frontal; N, Nasal; Pm, Pre Maxila; Z, Zygomatic; Md, Mandible; C, Clavicle; H, Humerus; R, Radius; U, Ulna; Ri, Ribs; Ti, Tibia; Fi, Fibula; I, Ilium; Fe, Femur; Sq, Squamosal; A, Atlas; Eo, Exocipital; So, Supraocipiltal; Ip, Interperitonial; P, Parietal.

Pakistan Journal of Zoology

April

Pakistan J. Zool., Vol. 56, Iss. 2, pp. 503-1000

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