EFFECT OF ESTROGEN AND TESTOSTERONE ON THE GASTRIC SECRETION OF RATS AND CONCIOUS RABBITS B.B. MAITRYA. S. GAHLOT AND B. MAITRYA

Similar documents
(Received 12th June 1968)

SEX Stereo Exercise and Oestrogen Pellet Enhancement

Short Synacthen Test for the Investigation of Adrenal Insufficiency

CHAPTER 2 MATERIALS AND METHODS

Digestion, Absorption. How & where?


Chapter 25. The Stomach Microscopic Anatomy and Gastric Function

Sex Hormone Testing by Mass Spectrometry

Upper Gastrointestinal Tract KNH 406

Digestion, Absorption. How & where?

FACT SHEET TESTETROL, A NOVEL ORALLY BIOACTIVE ANDROGEN

RATE OF EXCRETION OF N 15 AFTER FEEDING N16-LABELED /-ASPARTIC ACID IN MAN BY HSIEN WU AND SELMA E. SNYDERMAN

Human Clinical Study for Free Testosterone & Muscle Mass Boosting

Probiotics for the Treatment of Adult Gastrointestinal Disorders

General Structure and Function of the Digestive System

were shown (1).- Figure 3 shows four typical levels, of intravenous administration of glucose (5). Figure 4 shows a typical result obtained after

against allergic symptoms thought to be histaminic during a period of 1% minutes. No side effects When a dose of 30 mgm. of benadryl in 50 ml.

402 Adopted: 24 Feb 1987

Cyclooxygenase and NSAIDs

Digestive System Digestive Tract

Free Testosterone Cat# 2924Z

GI TRACT ORGANS ACCESSORY ORGANS

Vitamin U Therapy of Peptic Ulcer

Short Duration High-Level Exposure to Halon Substitutes: Potential Cardiovascular Effects

25-hydroxyvitamin D: from bone and mineral to general health marker

Consumer Concerns About Hormones in Food

Reproduction and its Hormonal Control

IV solutions may be given either as a bolus dose or infused slowly through a vein into the plasma at a constant or zero-order rate.

SECRETION IN RODENT SEMEN COAGULATION

Omega-3 fatty acids improve the diagnosis-related clinical outcome. Critical Care Medicine April 2006;34(4):972-9

Endocrine Responses to Resistance Exercise

Hormonal Oral Contraceptives: An Overview By Kelsie Court. A variety of methods of contraception are currently available, giving men and

UNIVERSIDAD DE GUAYAQUIL DEPARTMENT OF CHEMICAL SCIENCES

B12 & Cobalamin. Learning objectives

UNIVERSIDAD DE GUAYAQUIL DEPARTMENT OF CHEMICAL SCIENCES

Molar Mass of Butane

Canine Hypoadrenocorticism. Diagnosis and Treatment

A list of FDA-approved testosterone products can be found by searching for testosterone at

INFERTILITY/POLYCYSTIC OVARIAN SYNDROME. Ovulatory Dysfunction: Polycystic ovarian syndrome (PCOS)

Studies on Prostatic Cancer

THE DIGESTIVE SYSTEM Secretion Graphics are used with permission of: Pearson Education Inc., publishing as Benjamin Cummings (

Anatomy and Physiology of Human Reproduction. Module 10a

Historical Basis for Concern

SMALL AND LARGE INTESTINE SECRETIONS

Each gland has at least one duct that takes saliva to the oral cavity.

Subcutaneous Testosterone-Anastrozole Therapy in Breast Cancer Survivors ASCO Breast Cancer Symposium Abstract 221 Rebecca L. Glaser M.D.

Functions of the GI Tract. Chapter 18. Functions of the GI Tract (continued)

NIMULID MD. 1. Introduction. 2. Nimulid MD Drug delivery system

BILIOPANCREATIC DIVERSION WITH DUODENAL SWITCH SURGERY

The Menstrual Cycle. Model 1: Ovarian Cycle follicular cells

(From the Department of Biochemistry, University of Nebraska College of Medicine, Omaha)

Digestive System (continued) Digestive System. Stomach. Peptic Ulcer Disease

Testosterone for women, who when and how much?

BIOL 305L Laboratory Two


Dietary Fat Supplements and Body Condition: Does Fatty Acid Profile Matter? James K. Drackley, Professor of Animal Sciences

Effect of Insulin and Epinephrine on the Eosinophil and Blood Glucose Levels in Sheep; Lack of Diurnal Rhythm

Mammalian digestive tracts

Testosterone levels as modi ers of psychometric g

Creatine. Overview. Travis Harvey, PhD, CSCS

Education. Panel. Triglycerides & HDL-C

Figure 5. Energy of activation with and without an enzyme.

Green Principles Atom Economy Solventless Reactions Catalysis

10.2 The Human Digestive System pg. 411

Digestive System Lecture 5 Winter 2014

INTRODUCTION TO HORMONES

Fighting the Battles: Conducting a Clinical Assay

The Digestive System. You are what you eat!

Omeprazole 20 mg gastro-resistant tablets PL 14017/0277

THE DIGESTIVE SYSTEM

Use Of Testosterone In Men With Prostate Cancer. Traditional view: T is dangerous for PCa

Surgical Treatment of Obesity: A Surgeon s View

STUDIES ON ANTI-INFLAMMATORY AND ANALGESIC ACTIVITIES OF EUPHORBIA TIRUCALLI L. LATEX

Testosterone Therapy for Women

Effect of radiomimetic agents on two varieties of Trigonella with emphasis on plant height and pod numbers

1. What has a higher stored energy potential per gram, glycogen or triglycerides? Explain.

WHEY PROTEIN IMPORTANCE. Dan Phillips

Advances in Steroid Panel Analysis with High Sensitivity LC/MS/MS. Kenneth C. Lewis 1, Lisa St. John-Williams 1, Changtong Hao 2, Sha Joshua Ye 2

HDL Cholesterol Subfractions and the Effect of Testosterone Replacement in Hypogonadism

Efficacy and Safety of Insulin Aspart in Patients with Type 1 Diabetes Mellitus

Bonus Supplement plement Formula Testosterone Booster

Recommended Dose Volumes for Common Laboratory Animals IQ 3Rs Leadership Group - Contract Research Organization Working Group

Prevalence Diagnosis and Treatment of Hypogonadism in Primary Care Practice by Culley C. Carson III, MD, Boston University Medical Campus

Unit B Understanding Animal Body Systems. Lesson 1 Understanding Animal Digestion

THE TIMES OF OCCURRENCE OF MESOTHELIOMAS IN RATS FOLLOWING INOCULATION WITH ASBESTOS

THE EFFECT OF SODIUM CHLORIDE ON THE GLUCOSE TOLERANCE OF THE DIABETIC RAT*

Chapter 17 Digestive System. Alimentary Canal. Movements of the Tube

ab Free Testosterone ELISA Kit

Topic: Male Factor Infertility

DIURNAL VARIATIONS OF HEMOGLOBIN IN THE BLOOD OF NORMAL MEN

Artemisinin in Cancer Treatment. Dr. Narendra P. Singh Department of Bioengineering University of Washington Seattle

Vertical Sleeve Gastrectomy (VSG) - Also known as Sleeve Gastrectomy, Vertical Gastrectomy

Varicocele: To Fix or Not to Fix? That is the Question. Edmund S. Sabanegh, MD

The sensitive marker for glomerular filtration rate (GFR) Estimation of GFR from Serum Cystatin C:

P R O D U C T S CATALOG

Testosterone in Old(er) Men

UNIVERSIDAD DE GUAYAQUIL DEPARTMENT OF CHEMICAL SCIENCES

Yamaguchi University, Japan

Free Testosterone. Cat# 2924Z. Direct immunoenzymatic determination of Free Testosterone in serum or plasma. Free Testosterone ELISA Method

COULD IT BE LOW TESTOSTERONE?

Transcription:

EFFECT OF ESTROGEN AND TESTOSTERONE ON THE GASTRIC SECRETION OF RATS AND CONCIOUS RABBITS B.B. MAITRYA. S. GAHLOT AND B. MAITRYA Department of Phvsioloqv and Biochemistry, Sardar Patel Medical College, Bikaner-334001 Summary: Shay rats and conscious rabbits were used to study the effect of sex hormones on gastric secretion. Daily injections of estradiol-di-propionate and testosterone-propionate were given separately to each set of animals. while the control animals received solvent alone for the same duration of time. Estrogeninhibited gastric acid output but augmented the mucus secretion as evidenced by increased hexosamine and fucose contents; and testosterone had the reverse effects. The effect of estrogen was more potent than that of testosterone. An inverse relationship between gastric acid and mucus secretion hasbeen noted. Peptic activity varied independently of the acid output. These hormones seemed to vary the acid output bv modifying the composition of mucus secretion. Key words: Shay rats hexosamine acid output fucose peptic activity sex hormones glycoproteins augmented histamine stimulated gastric secretion INTRODUCTION A correlation between sex hormones and gastric secretion has been described (1,19). Incat. estrogen was shown to reduce gastric acid secretion (6). No such effect was reported inmonkey (9). dog (7) and rat (5). Under conditions of maximal histamine stimulationmale guineapigs secreted significantly higher amounts of gastric acid than the females(23). Stilboesterol therapy depressed gastric secretion in cats of either sex (17), butnot in dogs (3). Myhre (16) reported that estorgen produced no demonstrable effect on thehealing of experimental gastric ulceration in rats. while Griffen et al. (7) observed that histamineinduced ulcers in dogs were enhanced by it. A promoting effect of female sex hormoneon the development of gastric ulcer has been claimed in pylorus-ligated rats (2). Kowalewskiet al. (12) recorded that androgens enhanced the susceptibility of rat's gastric mucosato peptic action of gastric juice. In view of these conflicting reports regarding the action of sex hormones on gastric secretion,this study was conducted in rats and rabbits. MATERIALS AND METHODS Studies in rats: Normal. healthy, adult albino rats weighing between 200-250 g wereused. They were divided into (i) male, and (ii) female groups. Each group was

106 Maitrya et al. further subdivided into the following subgroups of 10 rats each: (a) Normal. control. (b) Estrogen. and (c) Testosterone. Estrogen rats werei jected im estradiol-di-propionate (Ovocvclin-Ciba). 10 p.g/kg/day. and testosterone trea rats received testosterone propionate (Perandran-Ciba). 100,.,.g/kg/day for 10 days. control experiments the solvent used for dissolving these hormones was injected for the sa duration of time. Gastric juice in 24-hr fasted rats was collected by ligating the cardiaca pyloric ends as described by Shay et al.(20). Kav's augmented histamine stimulated gas secretion (10) was collected for 2 hr and its volume. total acid output (TAO), and pep activity (8) were determined. Studies in rabbits: Normal. healthy, albino. adult rabbits of either sex, weighi between 1.5-2.0 kg fed on Hind Lever feeds and green foliage, were used. 10 rabbits each sex underwent three types of treatments, hence were classified into: (a) normal.(b estrogen. and (c) testosterone animals. Normal group were injected with t solvent of these hormones for 15 days. Then they were injected 20,.,.g/kg/day of Ovocycr for 15 days, and constituted the estrogen group. After this therapy, their gastr' samples were analysed, and they were given a rest for 10 weeks to enable them to rest their normal original gastric parameters. In the third stage, they received 200 ILg/kg/d of Perandren for 15 days, and formed the testosterone group. After each treatment Kav's augmented histamine stimulated gastric secretion (10 was collected from conscious, 24-hr fasted rabbits by passing 3-mm polvthelene tube ora by the technique developed in this laboratory. Gastric samples for 2 hr was collected an pooled. Its volume. free acid output (FAO), total acid output (TAO), pepsin (8), hexosamine (25) and fucose (4) contents were estimated. Under both these groups the animals were not used during estrous. and the dosage and duration of therapy were established after trial and error to yield the optimum results, RESULTS AND DISCUSSION Table I shows that estrogen in male rats caused significant reduction in gastric seen tion volume and its acid output. Similar results were obtained in female rats except for the fact that the volume of gastric secretion was not reduced significantly. In female rats, testesterone produced a significant rise in acid output and a fall in peptic activity but the changes were not Significant in male rats. Table 11 also indicates that estrogen inhibited significantly the volume, free and total acid outputs but augmented the hexosamine and fucose fractions of gastric juice in both the

Estrogen, Testosterone and Gastric Secretion 107 TABLE I: Effect of sex hormones on gaslric secretion of rats. Volume ml/2 br TAO meq/2 Peptic activity unitslmt ------------ 0::...- _ hr FEMALE RATS 0.93±1.210 (0.5-1.5) 0.026±0.0045 (0.012-0.045) 105.5±9.56 (70-150) 0.73±0.101 (05-1.5) 0.011±0.0012 (0.007-0.020) 109.9±4.17 (90-134) 0.99±0.127 (08-1.8) O. 035±0. 0032 (0.019-0.052) 95.8±5.05 (66-120) 0.92±0.190 (0.5...:...2.5) MALE RATS O. 035±0. 0048 (0.014-0.064) 119.1±16. 79 (50-192) o 62±0057 (05-1.0) O. 024±0. 0022 (0.017-0.040) 112.5±9.02 (70-150) 0.94±0 086 o 028 ±O. 0030 110.5±12.48 (0.6-1.2) (0.020-0.040) (56-180) --------------------------------------------------------- Total number of rats in each group were 10: Values are Mean ±SE: Figcrres in parentheses indicate the range. "denotes significant p values. sexesof rabbits. Testosterone significantly elevated the FAO in female rabbits and reduced thefucose contents of gastric juice in both the sexes of animals. In both the species of animals studied, estrogen inhibited the gastric secretion and testosteroneaugmented it though the former exercised more potent effect than the latter. Aninverse relationship between gastric acid output and mucus secretion has been noted. Peptc activity varied independently of the acid secretion. Hexosamine and fucose fractions of gastric secretion has been identified as major constituents of gastric mucus and boththese glycoproteins represented biochemically the amount of mucus present in it (12). Dueto lesser volume of gastric secretion in rats. these fractions could not be estimated. Several reports (1,13,19) indicated that estrogen exerted inhibitory effect on gastric secretion,while testosterone had the reverse effect. Our study also corroborated these findings,though contrary results in dogs (24) and rats (2) have been mentioned. and even some

103 Maitrva et at TABLE 11: Effect of sex hormones on gastric secretion of rabbits. Ind. J. Group Volume ml/hr fao meg/hl TAO meq/hl Pepsin unitlmt Hexosamine mg/1co ml FEMALE RABBITS Normal 15.1±0.2 (14-16) 0.9±0 3 (0.8-1.2) 1.1±01 (1.0-1.3) 45±1.3 (37-51) 14.1±02 (13.2-15.4) Estrogen 14.1±0.2 0.7±0 1 08±0.1 43±1.5 208±1.7 (13-15) (0.5-0.8) (0.6-0.9) (37-51) (16.2-28.8) Testosterone 16.2±0.2 1.1±0 3 1.2±0.2 41±1.9 134±0 1 (15-17) (0.9-1.5) (0.9-1.6) (31-48) (13.0-14.1) MALE RABBITS Normal 16.8±0.4 (15-19) 1.2±0.2 (0.9-1.6) 1.4±0.1 (1.0-1.7) 45±1.6 (40-55) 14.1±0.1 (13.1-14.7) Estrogen 14.3±0.3 (13-16) 0.9±0.1 (0.6-1.1 ) 0.9±0.1 (0.7-:-1.2) 50±1.8 (38-59) 20.6±1.7 23.9±U (15.6-28.8) (18.9-31.01 Testoster one 164±0.4 (14-18) 1.2±02 (1.0-1.6) 1.4±0.2 (1.1-1.8) 48±2.0 (42-60) 13.0±0.3 (11.2-14.1) 10 rabbits of either sex were used: Values are Mean ±SE: Figures in parentheses indicate range; 'denotes significant p values. authors described them to be without effect in dog (7), monkey (9) and man {18,21). Singh and Shukla (22) demonstrated correlation between sex hormones and gastric mucus secretion. Kowalewski (11) noted diminution in the secretion of mucopolysaccharides in rat's stomach after androgens. Menguy (15) reported that some hormones were known to influence the 'protective gastric mucus barrier' and androgen was labelled to be one of them. There are two mechanisms (14) responsible for bringing about variations in gastric acid secretion: (i) changes in mucus, and (ii) changes in parietal cell mass. In this study estrogen caused reduction in acid output and a rise in mucus secretion, while testosterone produced the opposite effects. These hormones, thus seemed to modify the gastric acid secretion by varying its mucus secretion. Peptic activity, however, varied independently of the acid secretion.

ume 23 ber 2 REFERENCES Estrogen. Testosterone and Gastric Secretion 109 Amure. B.O. and AA Omole. Sex hormones and acid secretion induced with carbachol. histamine and gastrin. Gut. 11 : 641-645. 1970. Antonsen. S. The influence of sex hormones on experimentally produced gastric ulcers in rats. Acta EnooCIInot; 19 : 203-208. 1955.. Baron. J. H. Sex. sex hormones and gastric secretion. Gut, 7 : 709-711.1966. Dische. Z. and L. B. Shettles. A specific colour reaction of methyl pentoses- and a spectrophoto-metric micromethod for their determination. J. Bioi. Chem., 175 : 595-603. 1948. Eisenberg. M.M. J.E. Owens and E.R. Woodward. Androgenic effect on gastric secretion. Surg. Forum. 15 : 321-323. 1964. Eisenberg. M.M.. J.E. Owens and E.R. Woodward. Effect of a synthetic androgen (Testosterone B-cyclopentyl-propionate) on denervated canine gastric pouches. Am. SUlg. 31 : 135-138. 1965. Griffen. W.O. Jr. 0,. M. Nicoloff. N. H.Stone and O. H. Wangensteen. Role of sex hormones on peptic ulcer. FlDc. Soc. Exper. BioI. Med. 106: 101-104. 1961. Hunt. J. N. A method for estimating peptic activity in gastric contents. Biochem. J., 42 : 104-109. 1948. Kaufmann. H. J. and H. M. Spire. Oesterogens and gastric secretion. Gssttoent.. 54 : 913-917. 1968. Kay. A W. Effect of large doses of histamine on gastric secretion of HcI. an augmented histamine test. Brit. Med. J., 2 : 77-80. 1953. Kowalewski. K. Effect of certain androgenic steroids and cortisone. on gastric ulcerogenesis in fasting rats. Floc. Soc. Expel. BioI. Med.. 101 : 147-148. 1959. Kowalewski. K.. J. F. Schier and G. Chmura. Effect of sex hormones on gastric secretion and on mucosa in cophorectomized histamine stimulated rats. Digestion. 3 : 13-19. 1970. l.andor. J.H. and R. A Wild. oestrous and gastric secretion in dog. Gut, 2 : 855-858.1970. Maitrva. B. and B. B M aitrya. Effect of estrogen and testosterone on the augmented histamine stimulated gastric secretion of intact and castrated rats. Ind. J. Exper. Biol., 16 : 558-560. 1978. Menguy. R. Gastric mucus and gastric mucous barrier. Am. J. SUlg. 117 : 806-812. 1969. Myhre. E. Regeneration of the fundic mucosa in rats: Effect of ssuone and of castration. A.M.A. Arch. Peth., 62 : 30-36. 1956. Oiha. K. N. and D. R. Wood. The inhibitory effect of stilboesterol on gastric secretion in cats. Brit. J. Fhetm. 5: 389-394. 1950. Parbhoo. S.P. and I.D.A. Johnston. Effects of oesterogens and progestogens on gastric secretion in patients with duodenal ulcer. Gut, 7 : 612-618. 1966. Sandweiss. D. J. H. C. Saltzstein and A A Farbman. The relation of sex hormones to peptic ulcer. A:n. J. Digest. oo.. 6 : 6-12. 1939. Shav, H. D.C.H. Sun and M. Gruenstein. A quantitative method for measuring spontaneous gastric secretion in the rat. Gestroent., 26 : 906-913. 1954. Schiff. L.. H. Felson. J. Graff and B. Meyer. The effect of exogenous hormone on gastric acidity. Am. J. Digest. Dls. 5 : 292-294. 1938. Singh. G.B. and R. C. Shukla. Effect of gonadectomy on experimental peptic ulceration. Ind. J. Med. Hes., 47 : 287-293. 1959. Voith. K. and B. A Kovacs. Differences in gastric output in response to histamine between male and female guineapigs. Canad. J. Pbvsicl. Phstm., 44 : 515-520. 1966. Winkelstein. A. Observations on ulceration adjacent to experimental gastric pouches in dogs. Am. J. Digest DIS., 3 : 229-231. 1936. Winzler, R. J. Determination of serum glycoproteins. In 'Methods of Biochemical Analysis'. by Glick. D. New York. Interscience Publishers, 279-311. 1958.