EVALUATION OF FOLLICULAR ATRESIA AND ELECTROPHORETIC PATTERN OF FOLLICULAR FLUID PROTEINS IN ACYCLIC BUFFALO (Bubalus bubalis)

Similar documents
Ovarian follicular dynamics during estrous cycle and its aberrations during certain reproductive disorders in buffalo

M. Irfan-ur-Rehman Khan, M. A. Rana and N. Ahmad. Department of Theriogenology, University of Veterinary and Animal Sciences, Lahore, Pakistan

IN OVARIAN ANTRAL FOLLICULAR FLUID OF BUFFALOES*

OVARY The surface of the ovary is covered with surface epithelium

Theriogenology Department, Faculty of Veterinary Medicine, Beni Suef University, Egypt 2

MINERAL PROFILES OF OVARIAN ANTRAL FOLLICULAR FLUID IN BUFFALOES DURING FOLLICULAR DEVELOPMENT*

HISTOLOGICAL CHARACTERISTICS OF FOLLICULOGENESIS IN MURRAH WATER BUFFALOES DURING THE EARLY POSTPUBERTAL PERIOD

Occurrence of polyovular follicles and its possible significance in the ovary of the bat, Scotophilus heathi

Ovarian Follicular Development in the Untreated and

Oxidative stress during cystic ovarian disease in water buffalo

In Situ Localization of Apoptosis in the Rat Ovary during Follicular Atresia'

BIO-CHEMICAL MILIEU OF BUFFALOES OVARIAN FOLLICLES DURING THEIR DEVELOPMENT*

The role of growth factors in regulating cellular events during ovarian follicular development Leon J. Spicer

Albumin Fractions from Different Species Stimulate In Vitro Progesterone Production by Granulosa Cells in Buffalo

Pakistan Veterinary Journal

Animal Science 434! Tonic and Preovulatory Surge of GnRH! Tonic and Preovulatory Surge of GnRH! Lecture 11: The Follicular Phase of the Estrous Cycle!

Effect of PMSG on follicular atresia in the immature rat

Effect of Gonadotrophins and Gonadotrophin Releasing Hormone (GnRH) on folliculogenesis in the domestic pigeon, Columba livia.

Ovarian Remnant Syndrome

CLARITY reveals dynamics of ovarian follicular architecture and vasculature in three-dimensions

EFFECT OF DRYING ON PROTEIN PROFILE OF MURRAYA KOENIGII LEAVES S. Satheshkumar 1* and N. Punniamurthy 2

Synchronization of Ovulation and Fixed-Time Insemination for Improvement of Conception Rate in Dairy Herds with Poor Estrus Detection Efficiency

Relationship between Energy Expenditure Related Factors and Oxidative Stress in Follicular Fluid

Morphometric analysis of ovarian follicles of Black Bengal goats during winter and summer season

SUPEROVULATORY RESPONSE IN SUMMER ANESTRUS BUFFALOES AND CATTLE TREATED WITH ESTRUS SYNCHRONIZATION PROTOCOL ABSTRACT

Chapter 27 The Reproductive System. MDufilho

Deficient Proliferation and Apoptosis in the Granulosa and Theca Interna Cells of the Bovine Cystic Follicle

EFFECT OF TWO DIFFERENT DOSES OF FSH-P (FOLLTROPIN-V) ON SUPEROVULATION IN BERARI (NAGPURI) BUFFALOES (Bubalus bubalis)

Expression of mrnas encoding tumor necrosis factor-α and its receptor I in buffalo ovary

AN IMMUNOHISTOCHEMICAL AND ULTRASTRUCTURAL STUDY OF THE OVARY OF THE IMMATURE OSTRICH (STRUTHIO CAMELUS) WAHABU HAMISI KIMARO

Reproductive cyclicity 19. Introduction. Page 1. repro and its story lines. Male repro: a simpler way of control

ULTRASONOGRAPHIC BIOMETRY OF THE OVARY AND ITS RESPONSES DURING SUPEROVULATION IN TODA BUFFALOES

CASE 41. What is the pathophysiologic cause of her amenorrhea? Which cells in the ovary secrete estrogen?

SUMMARY. Keywords: quail, Coturnix japonica, morphology, ovary, oviduct, neurotrophins, immunohistochemistry

Effect of Resistin on Granulosa and Theca Cell Function in Cattle

LH and FSH. Women. Men. Increased LH. Decreased LH. By Ronald Steriti, ND, PhD 2011

THE MENSTRUAL CYCLE INA S. IRABON, MD, FPOGS, FPSRM, FPSGE OBSTETRICS AND GYNECOLOGY REPRODUCTIVE ENDOCRINOLOGY AND INFERTILITY

Female Reproductive System. Justin D. Vidal

REPRODUCTION & GENETICS. Hormones

Influence of large follicles on oestrus induction and ovulation after embryo collection in superovulated Japanese Black cows

A263 A352 A204. Pan CK. pstat STAT3 pstat3 STAT3 pstat3. Columns Columns 1-6 Positive control. Omentum. Rectosigmoid A195.

Evaluation of Ovarian Follicular Health with the Markers of Endothelial and Granulosa Cells

Levels of heat shock protein transcripts in normal follicles and ovarian follicular cysts

Impact of High-Fat Environment on Ovarian Androgen Synthesis in Rats and the Associated Pathophysiological Changes

Development Supplementary information. Supplementary Figures * * +/+ +/- -/- +/+ +/- -/-

OVARIAN FOLLICLE POPULATION AND FOLLICLE SIZE IN ANATOLIAN WATER BUFFALOES 111

The reproductive lifespan

Syncrostim. The second chance for open cows. Presented for single cow treatment

Title. Author(s)KANAGAWA, Hiroshi. CitationJapanese Journal of Veterinary Research, 11(2): Issue Date Doc URL. Type.

The intra-follicular molecular biology mandating advancement of egg retrieval in some women

REPRODUCTIVE CYCLE OF FEMALE MAMMAL

Buffalo Bulletin (September 2013) Vol.32 No.3. Original Article

Iranian Journal of Veterinary Research, Shiraz University, Vol. 13, No. 1, Ser. No. 38, 2012

Effects of modified FSH surges on follicle selection and codominance in heifers

Proceedings, The Applied Reproductive Strategies in Beef Cattle Workshop, September 5-6, 2002, Manhattan, Kansas

International Journal of Science, Environment and Technology, Vol. 7, No 6, 2018,

Research Article Efficacy of Tuohy Needle in Oocytes Collection from Excised Mare Ovaries

JSAR Young Investigator Award. Studies of Follicular Vascularity Associated with Follicle Selection and Ovulation in Cattle

Gonadotropin Regulation of Rat Ovarian Lysosomes" Existence of a Hormone Specific Dual Control Mechanism

Pinpoint Slide RNA Isolation System II Catalog No. R1007

Supplementary Note. Nature Genetics: doi: /ng.2928

Article Artikel. F E van Niekerk a and C H van Niekerk a

Differential Fertility in Dairy Buffalo: Role of Thyroid and Blood Plasma Biochemical Milieu

FREE-ROAMING HORSE AND BURRO FERTILITY CONTROL WORKSHOP Albuquerque, NM November 8, 2018

Ovarian follicular development in cattle

Destruction of the Germinal Disc Region of an Immature Preovulatory Chicken Follicle Induces Atresia and Apoptosis 1

The menstrual Cycle. François Pralong

Treatment 3 Days After Ovulation In Mares

Abstracts for the KSAR and JSAR Joint Symposium. Fertility control in female domestic animals: From basic understanding to application

Ovarian Dysfunction in Dairy Cows

Manish Banker. Declared receipt of grants; member of a company advisory board, board of director or similar group

Vascular endothelial growth factor receptor 2 mediated angiogenesis is essential for gonadotropin-dependent follicle development

LH (Bovine) ELISA Kit

Contributions to Anatomic Pathology, over the years

Kulnasan Saikhun 1 and Kampon Kaeoket 2

Page 1. A wide variety of ovarian abnormalities are encountered in clinical practice

Why Cycle Control? Manipulating Ovulation and Estrous Synchronization. Manipulating Ovulation. Cattle. Principle of PGF 2a Use

Sulpiride-Induced Hyperprolactinemia in Mature Female Rats: Evidence for Alterations in The Reproductive System, Pituitary and Ovarian Hormones

Factors affecting number of surface ovarian follicles and oocytes yield and quality in egyptian buffaloes

CHAPTER 7: REAGENTS AND SOLUTIONS

ALAEZI CM 1 *, ADISA JO 2, OKOROCHI EC 3 and OKECHI OO 4

ENDOCRINE CHARACTERISTICS OF ART CYCLES

Classification of Bovine Reproductive Cycle Phase using Ultrasound-Detected Features

Collection of oocytes through transvaginal ultrasound-guided aspiration of follicles in an Indian breed of cattle

Superovulatory Response in Relation to Follicular Dynamics and Presence of Dominant Follicles in Egyptian Buffaloes

Apoptosis and active caspase-3 expression in human granulosa cells

Schedule of Accreditation issued by United Kingdom Accreditation Service 2 Pine Trees, Chertsey Lane, Staines-upon-Thames, TW18 3HR, UK

APPENDIX 1 ETHICAL CLEARANCE

AnS 214 SI Multiple Choice Set 4 Weeks 10/14-10/23

The menstrual cycle. François Pralong

Ovarian fecundity in patients with endometriosis can be estimated by the incidence of apoptotic bodies

Histochemical Studies of Pancreas in Prenatal Goat (Capra hircus)

Effect of the Dominant Follicle Aspiration before or after Luteinizing Hormone Surge on the Corpus Luteum Formation in the Cow

Two important cells in female are the theca cells and the granulose cells. Granulosa cells are affected by the two gonadotropin hormones; FSH and LH.

EFFECTS OF SOME PESTICIDES ON THE EMBRYONIC STAGES OF CHICK

Selection of the dominant follicle in cattle and horses

Purification of heparin binding oviduct specific proteins and its effect on in vitro embryo development in cattle

HiPer Western Blotting Teaching Kit

Product Contents. 1 Specifications 1 Product Description. 2 Buffer Preparation... 3 Protocol. 3 Ordering Information 4 Related Products..

Title. CitationAnimal Science Journal, 88(11): Issue Date Doc URL. Rights. Type. File Information

Transcription:

Original Article Buffalo Bulletin (December 2013) Vol.32 No.4 EVALUATION OF FOLLICULAR ATRESIA AND ELECTROPHORETIC PATTERN OF FOLLICULAR FLUID PROTEINS IN ACYCLIC BUFFALO (Bubalus bubalis) F.A. Khan 1,*, G.K. Das 1, Megha Pande 1, Rajendra Singh 2 and S.K. Ghosh 3 ABSTRACT follicle, atresia, follicular fluid Histological examination of H&E stained sections of ovaries collected from cyclic and acyclicbuffaloes (n=6/group) was done in order to evaluate the degree of follicular atresia. The percentages of healthy and atretic follicles were different (P<0.05) between cyclic (53.1% and 46.9%, respectively) and acyclic (10.7% and 89.3%, respectively) buffaloes. Electrophoretic patterns of follicular fluid proteins, studied by SDS-PAGE of follicular fluid samples aspirated from small (5.0-6.9 mm), medium (7.0-9.9 mm) and large ( 10 mm) follicles of cyclic and acyclic buffaloes (n= 6/group), did not reveal any apparent differences between the groups. DNA fragmentation patterns evaluated by using DNA isolated from the cell pellets obtained after centrifugation of the follicular fluid samples from small-, medium- and largesized follicles of cyclic and acyclic buffaloes (n=5/ group) showed a typical apoptotic oligonucleosome ladder pattern in the acyclic group. In conclusion, these results indicate an increased rate of follicular atresia without any qualitative changes in the follicular fluid proteins during ovarian acyclicity in buffalo. Keywords: buffaloes, Bubalus bubalis, ovary, INTRODUCTION Follicular development in buffalo is a continuous process with concurrent growth and regression of ovarian follicles occurring during the reproductive cycle. Similar to those in cattle, follicular dynamics in buffalo follows a wave pattern with predominance of two-wave cycles (Baruselli et al., 1997). During each follicular wave, there is recruitment of a group of follicles (cohort) out of which usually one is selected for progressive growth to become the dominant follicle while the others undergo regression. Dominant follicles can have variable fates-ovulation, persistence or atresia, depending upon several factors like physiological state, stage of the cycle, pathological conditions or hormonal treatments etc. An increased rate of follicular atresia has been implicated as one of the major factors for reproductive failure in buffalo (Rajesha et al., 2001). Atresia of ovarian follicles is associated with various morphological, biochemical and histological changes (Kaipia and Hsueh, 1997). A recent study on the follicular characteristics during ovarian acyclicity in buffalo showed that all the large-sized ( 10 mm) follicles 1 Animal Reproduction Division, Department of Pathobiological Sciences, 1656 Linden Drive University of Wisconsin-Madison, Madison, WI 53706, *E-mail: fakhan3@wisc.edu 2 Centre for Animal Disease Research and Diagnosis 3 Germplasm Centre, Indian Veterinary Research Institute, Izatnagar 243122, India 265

are estrogenically inactive, which indicates a derangement in the normal follicular development culminating in follicular atresia rather than ovulation (Khan and Das, in press). Studies on biochemical composition of the follicular fluid demonstrated alterations in certain components like nitric oxide, ascorbic acid, glucose, cholesterol and alkaline phosphatase during acyclicity in buffalo leading to the conclusion that oxidative stress caused by the imbalance of nitric oxide and ascorbic acid possibly results in follicular atresia manifested as inactive estrogen status and increased alkaline phosphatase levels in the follicular fluid (Khan and Das, in press; Khan et al., 2011). Available evidence suggests that follicular fluid protein concentrations are not affected by the reproductive state of the animal (Khan et al., 2011). However, the effect of acyclicity on the electrophoretic pattern of follicular fluid proteins remains unknown. The objectives of the present study were to evaluate follicular atresia in ovarian follicles of acyclic buffaloes using ovarian histology and DNA fragmentation patterns (oligonucleosome ladder pattern) characteristic of apoptosis, and to examine the changes in the electrophoretic pattern of follicular fluid proteins during acyclicity in buffalo. MATERIALS AND METHODS Ovaries were collected from cyclic and acyclic buffaloes (n=6/group) at a local abattoir and transported to the laboratory on ice within 30 minutes. The ovaries were fixed in 10 % formalin, embedded in paraffin wax, cut into thin sections of 5-7 μm thickness and stained with haematoxylin and eosin (H&E) using routine histological staining procedure (Luna, 1968). The stained slides were examined by light microscopy for histological characteristics of the ovarian follicles, especially the granulosa and theca cell layers. Classification of follicles into healthy and atretic was done as described previously (Guraya, 1979). Follicular fluid was aspirated from small, medium-sized and large follicles of cyclic and acyclic buffaloes (n=6/group), centrifuged at 1000 g and 4 C for 10 minutes and the supernatant was collected for analysis. The electrophoretic pattern of follicular fluid proteins was studied by a standard protocol (Laemmli, 1970) using 10% polyacrylamide gel in a vertical slab gel apparatus (Bangalore GENEI, India). For studying the apoptotic oligonucleosome pattern, the cell pellets obtained after centrifugation of the follicular fluid samples from small-, medium- and large-sized follicles of cyclic and acyclic buffaloes (n=5/group) were used. DNA was isolated using a DNeasy Kit as per the protocol recommended by the manufacturer (Quiagens Ltd.). For visualizing the probable presence of the oligonucleosome ladder pattern characteristically shown by apoptotic DNA fragments (Hermmann et al., 1994), 10 μl of DNA sample obtained was electrophoresed in 2% agarose gel containing 1 μg/ ml of ethidium bromide and visualized in a UV-Gel Documentation system (Syngene, UK). Comparison of percentage normal and atretic follicles between cyclic and acyclic groups was done by Chi-square test using STATS TM Version 1.1, Decision Analyst Inc., USA. REFERENCES AND DISCUSSION The percentages of healthy and atretic follicles were different (P<0.05) between cyclic (53.1% and 46.9%, respectively) and acyclic (10.7% and 89.3%, respectively) buffaloes. The concomitant 266

presence of both healthy and atretic follicles in cyclic buffalo ovaries indicates that growth and regression of follicles occur concurrently further confirming the previous observations that follicular development is a continuous process in buffalo (Baruselli et al., 1997). Based on the presence of an almost equal proportion of healthy and atretic follicles in cyclic buffaloes, it seems apparent that growth and regression of follicles occur at a similar rate during the estrous cycle. The presence of both healthy and atretic follicles in acyclic buffaloes provides support to our earlier notion that follicular development does continue during acyclicity as well (Khan and Das, in press). The predominance of atresia in acyclic buffalo ovaries is in line with observations during acyclicity based on estrogenic status (Khan and Das, in press) and the findings of Guraya (1979) who reported an increased incidence of atresia in buffalo ovaries during anestrus. A prominent apoptotic DNA fragmentation (oligonucleosome ladder) pattern was observed in DNA isolated from the granulosa cells and oocytes of all the three follicle size categories (Figure 1; lanes 1, 2 and 3) in acyclic buffaloes. In contrast, no such pattern was evident in the cyclic group (Figure 1; lanes 4, 5 and 6). The higher percentage of atresia indicated by the above results compared to the observations on histology can be inferred to be a reflection of changes occurring in the DNA earlier than the manifestation of the morphological alterations during follicular atresia. SDS-PAGE analysis of follicular fluid proteins did not reveal any apparent difference in the overall electrophoretic pattern between acyclic and cyclic groups (Figure 2). Pertinently, in an earlier study on the biochemical composition of follicular fluid (Khan et al., 2011), no difference in the total protein concentration was recorded between cyclic and acyclic buffaloes. Based on these observations, it can be concluded that there are no qualitative or quantitative alterations in the protein component of the follicular fluid during acyclicity in buffalo. In summary, results of the present study indicate an increased rate of follicular atresia characterized by histological alterations in the follicle and fragmentation of granulosa cell DNA without any characteristic change in the electrophoretic pattern of follicular fluid proteins during ovarian acyclicity in buffalo. ACKNOWLEDGMENTS The authors thank Drs. Prafull Singh, M.Y. Wani and S.R. Bisla for their help during DNA extraction and SDS-PAGE and the staff of the Division of Pathology, Indian Veterinary Research Institute for their assistance with the ovarian histology. REFERENCES Baruselli, P.S., R.G. Mucciolo, J.A. Visintin, W.G. Viana, R.P. Arruda, E.H. Madureira, C.A. Oliveira and J.R. Molero-Filho. 1997. Ovarian follicular dynamics during the estrous cycle in buffalo (Bubalus bubalis). Theriogenology, 47: 1531-1547. Guraya, S.S. 1979. Morphological and histochemical observations on buffalo ovaries during anoestrus. Indian J. Anim. Sci., 49: 423-432. Herrmann, M., H.M. Lorenz, R. Voll, M. Grunke, W. Woith and J.R. Kalden. 1994. A rapid and simple method for the isolation of apoptotic DNA fragments. Nucleic Acids Res., 22: 5506-5507. 267

Figure 1. Electrophoretic pattern of follicular fluid proteins (Lane M-Marker; Lanes 1-3: small, mediumsized and large follicles of the acyclic group, respectively; Lanes 4-6: small, medium-sized and large follicles of the cyclic group, respectively). Figure 2. Granulosa cell DNA fragmentation pattern (Lanes 1-3: small, medium-sized and large follicles of the acyclic group, respectively; Lanes 4-6: small, medium-sized and large follicles of the cyclic group, respectively). 268

Kaipia, A. and A.W. Hsueh. 1997. Regulation of ovarian follicle atresia. Annu. Rev. Physiol., 59: 349-363. Khan, F.A. and G.K. Das. 2012. Follicular characteristics and intrafollicular concentrations of nitric oxide and ascorbic acid during ovarian acyclicity in water buffalo (Bubalus bubalis). Trop. Anim. Health Pro., 44(1): 125-131. Khan, F.A., G.K. Das, Megha Pande, R.A. Mir and Uma Shankar. 2011. Changes in biochemical composition of follicular fluid during reproductive acyclicity in water buffalo (Bubalus bubalis). Anim. Reprod. Sci., 127: 38-42. Laemmli, U.K. 1970. Cleavage of structural proteins during the assembly of the heat of bacteriophage T4. Nature, 227: 680-685. Luna, L.G. 1968. Manual of Histological Staining Methods of the Armed Forces Institute of Pathology, 3 rd ed. McGraw-Hill Book Co., New York, USA. Rajesha, D., J.P. Ravindra and M. Narayanaswamy. 2001. Ovarian antral follicular activity and serum estradiol-17β concentrations in buffaloes during different periods of the year. Indian J. Anim. Sci., 71: 641-643. 269