The guinea pig (cava parellus), also called cavy, and the genus cavia. Despite their common name, these animals are not in the pig family, nor are they from guinea, they originated in the Andes, and earlier studies based on biochemistry and hybridization suggested they are domestic descendants of a closely related species of cavy such as Cavia aperea, C. fulgida, or c. tschudii and therefore do not exist naturally in the wild (Ounnum 2010). Guinea pigs were popular laboratory animals until the later 20th century; about 2.5 million guinea pigs were used annually in the U.S. for research in the 1960s. (Gad, 2007), but that total decreased to about 375,000 by the mid-1990s. as of 20007, they constitute approximately 2% of the current total of labory animals in the past they were widely used to standardize vaccines and antiviral agent they were also often employed in studies on the production of antibodies in response to extreme allergic reaction or anaphylaxis.
The most readily identified aspect of animal sexual behavior is the mounting response. It is an essential component of the male mating pattern but frequently occurs in females, especially during estrus. In a successful mating sequence the male mounts the female from the rear. The forelegs are placed on the back or around the sides of a female with the bind legs in the ground. The posture and motion permit the male to insert the exact penis into the females vagina not all mounting, however, in oriented to the rear of the female. The male may mount the female. The male may mount ths side or head of the partner and may or any not execute peptic thrusts; but in some species, such as the rat and dog mounting by females is not restricted to any particular part of the estrous cycle. The mount executed by a female is frequently indistinguishable from that of from that of the male. Thus, the typography of the behaviour does not identify the sex of the animal. Mounting occurs between members of the same or opposite sex and across species in some instances.
Male guinea pigs engage in several species. Eypical precopulatory behaviours, including nibbling the female’s fur on her head and neck, sniffing her amogenital regin,and making guttural sounds while either circling the female or shiffing his weight on his two rear feet while keeping his forepaws stationary. The male then approaches the female the rear, places his chest over the female’s back while claspring her sides, and begins petric thrusting, while usually results in a veginal intromission. Males can intromit at a rate of approximately 1 per minute, and so can ejaculate in a 15 mins test. Although a male that ejaculates with a single female usually does not reinitiate copulation within the next hour, he may copulate with a deferent tamale (Horm, 2007).
Cimetidine is an histamine H2-receptor antagonist that inhibits stomach acid production. It is largely used in the treatment of heartburn and peptic ulcers. It has been marketed by GlaxoSmithKline (which is selling the brand to prestige brands) under the trade name tagemet (sometimes tagemet HB or Tagamet HB 200). Cimetidine was approved UK in 1976 and was approved in the US by the food and Drug administration for prescriptions starting January 1, 1979.
Cimetidine, approved by the FDA for inhibition of gastric acid secretion, has been advacated for a member of dermatological disease. (Scheimfeld, 2003). Cimietidine was the prototypical histamine H2-receptor antagonist from which the later members of the class were developed. Cimmietidine was the culmination of a project at smith, klrin and French (SK & F; Moro claxosmithkhine) by James W. Black, C. Robin canetllin, and others to develop a histamine receptor antagonist to suppress stomach acid secretion (American chemical society, 2012). This was one of the first drugs discovered using a rational drug design approach. Sir. James w. black shared the 1988 Nobel prize in physiology or medicine for the discovery of proppranolol and also in credited for the discovery of cimetidine, actually the medicinal chemists would have made the discovery. (Silverman and Richard, 2004).
At the time (1964), his tamine was known to stimulate the secretion of stomach acid, but also that traditirt amithistamines had no effect on acid production. In the porcert, the SK & F scientist also proved the existence of histamine H2-receptors. The SK & F ream used a rational drug design structure starting from the structure of his tamine the only design lead, since nothing was known of the then hypthtical H2-receptor. Hundreds of modified compounds were synthesized in an effort to develop a model of the receptor. The first breakthrough was as-guanylhistamine, a partial H2-receptor anlagonist from this lead the receptor model was further refined and eventually let to the development of burianarmide, the first H2-receptor antagonist. Burimanide, a specific competitive antagonist at the H2-receptor, 100 times more potent than N-guanylhristamine, provide the existence of the H2-receptor. Burimamide was still insufficiently potent for oral administration and further modification of the structure, based on modifying the PKa of the compound, led to the development of metiamide. Metiamide was an effective agents. It was associated, however, with inacceptable nephrotoxicity and agranulocylosis (American chemical society 2012). Then toxicity was proposed to arise from the thourea group and similar guaidine analogues were investigated until the ultimate discovery of cimetidine was first marketed in the united kingdom in 1976, therefore, it took 12 years from initiation of the H2-receptor aotagonist program to commercialize. The commercial; name “tagamet” was decided upon by fusing the two words “anatagonist” and “cimietidine”. (American chemical society 2012) subsequent to the introduction onto the US dug market. Tow other H2-receptor antagonist were approved. Ranitidine (Anatac, Glaxo Labs) and cimetidine became the first drug ever to reach more than $ 1billion a year in sales, this making of the first blockbuster drug. (Volntney, Take, 2006) in a deating expected to take effect in 2012, Glaxosmithklme sold Tagement and 16 other grant to prectige brands. (Ranii, David. 2011).
In some studies cimetidine has beed fonnd to reduce the debilitating pain and symptoms of herpes zorter, presumably by blocking the H2-receptor of T-typrptocyte suppress or cells. (Faloon, et al 2001).
A number of “open label” studies showed cimietidine was effective in the treatment of common wards, but more rigorous double-blind clinical trials suggested it to be no more effective than a placeto. However, the researchers in this study admit their results may not be sound, due to small sample size, and did not explore brigher dosing options. (fit KE, William PC 2007) another study by yokogama, et al used cimietidine for the treatment of chronic calcific tendiritis of the shoulder, a (Yokogama2003). The small scale study too 16 individual with calcific tendimitis in one shoulder, all of which had previously attempted other forms to therapy, including steroid injection and arthroxcoptic lavage. During the course of the study, 10 patients reported an elimination of pain and a disappearance of calcium deposits with results being on a small scale, cimitidine, for the treatment of chrionic calcific trendrintis of the shoulder, has been recommended to be opened to large scale clinical trials (Masailo Skeletal pain 2008).
In asia, cimietidine, which molecularly targets EGF, VEGF and E-selection associated with sialylated leins biomakers and metastasis, has been combined with longer term continous low does. SFU (Matsumoto 2002) or metronomic tagefur-uracil chemotherapy for advanced epithetial cancers, with usually long survive (Marsumoto 2004) including for stage 111 colorectal cancers, (Matsumoto 2002) as well as refractory and recurrent cancers. Cimietidine has been reported for use as an anagelsic in experimental treatments of interestital cystitis pretreatment with cimietidine improves the accuracy of measured creatinine clearance testing when using urine collection analysis.
Cimetidine as a known intribitor of many isozymes of the cytpcrome P450 enzymes system. (Specifically CYP1A2, CYPWC9, CYP2E19, CYP206, CYP2E1, and CYP3A4). This inhibition forms the basis of the numerious drug interaction that occur between cimetidine and other drugs for example, cimetidine is a competitive antagonist at the dihydrotesterone (DHT) receptor, leading to exaggerated effects of estorgens, in women, this can lead to galectorrhea, whereas in men gynecomastia has been reported during post marketing surveillance in the 1980s. Cases of male sexual dysfumetion were also reported. Cimietidne also affects the metabolism of methadone, sometimes resulting in higher blood levels and a bright incidence of side effects, and may interact in the antimalarial medication hydroxychloroquire. Crimetidine is also known to potentiate the effects of several opioids which are partially metabolized via the cytochronic P450 pathway via inhibiting their metabolism and temporary decrease of liver function due to reduced hepatic blood flow. This can lead to extreme plasma levels of these drugs and can easily lead to a fatal over dose.
Antacid preparations such as cimetidine work by suppressing acid mediated break down of proteins, leads to an elevated risk to developing food or drug allergies. This happens due to undigested proteins then passing into the gastrointestinal tract where sensitization occurs. It is unclear whether this risk occurs with only long-term use or with short term use as well. (Pati-Scholl and Jensen-Jarolin, 2011) it is also important to recognize that cimetidine can interact with a number of different psychoactive medications, including those in the classes of Trcyclic antidepressants and selective serotonin reuptake inhibitors, causing incread blood levels of these drugs and subsequent toxicity. The development of longer acting H2-receptor antagonists with reduced adverse effects, such as ranitidine, proved to be the downfall of cimetidine and, though it is still used it is no longer among the more widely used H2-receptor antagonists. Side effect can include, dizziness, and more rarely, headache.
It have been reported that, naturally, during pregnancy, rooment od thave a burning sensation in the heart. However some assume it is ulcer, as such they take ulcer drugs, since cimetidine is one of the most common and effective ulcer drugs, it is administered to them either by self administration and although the unborn child, seemed to be protected, completely immured to some external and internal influence surrounding the mother, that could cause defilitating effect at different developmental stages. Cimetidine has been shown to be a teratogenic drug as a teratogenicf drug iti could cause serious abnormality during prenatal and postnatal live to offsprings of mother who used it during pregnancy. However this work/study is aimed at revealing the effect of cimetidine on offspring of mother who where exposed to ti during pregnancy.
This study aims to examine: If exposure to cimetidine will manifest any significant effect on the behaviour of their offsprings. If the intake of cimetidine during pregnancy have an effect on the birth weight of offspring. If the intake of cimetidine during pregnancy affect learning and memory in offsprings whose mother’s where exposed to cimetidine.
1.4 RELEVANCE OF STUDY
This study stands to reveal the teratogneic effect of cimetide on offspirngs of mothers who where exposed to it during pregnancy and it is mainly directed to pregnant women who self medicate during pregnancy as well as men and women who may not know till date the side effect of cimetidne intake. This research will serve as a guide to the medical practitioners (on how to administer doses of cimetidine, especially during pregnancy) as well as the general public on issues based on the teratogenic effect of cimetidine intake.
How do I get this complete project on THE TERATOGENIC EFFECT OF CIMETIDINE ON THE OFFSPRING’S OF ALBINO RATS?
Simply click on the Download button above and follow the procedure stated.
I have a fresh topic that is not on your website. How do I go about it?
How fast can I get this complete project on THE TERATOGENIC EFFECT OF CIMETIDINE ON THE OFFSPRING’S OF ALBINO RATS?
Within 15 minutes if you want this exact project topic without adjustment
Is it a complete research project or just materials?
It is a Complete Research Project i.e Chapters 1-5, Abstract, Table of Contents, Full References, Questionnaires / Secondary Data
What if I want to change the case study for THE TERATOGENIC EFFECT OF CIMETIDINE ON THE OFFSPRING’S OF ALBINO RATS, What do i do?
Chat with Our Instant Help Desk Now: +234 814 010 7220 and you will be responded to immediately
How will I get my complete project?
Your Complete Project Material will be sent to your Email Address in Ms Word document format
Can I get my Complete Project through WhatsApp?
Yes! We can send your Complete Research Project to your WhatsApp Number
What if my Project Supervisor made some changes to a topic i picked from your website?
Call Our Instant Help Desk Now: +234 814 010 7220 and you will be responded to immediately
Do you assist students with Assignment and Project Proposal?
Yes! Call Our Instant Help Desk Now: +234 814 010 7220 and you will be responded to immediately
What if i do not have any project topic idea at all?
Smiles! We've Got You Covered. Chat with us on WhatsApp Now to Get Instant Help: +234 814 010 7220
How can i trust this site?
We are well aware of fraudulent activities that have been happening on the internet. It is regrettable, but hopefully declining. However, we wish to reinstate to our esteemed clients that we are genuine and duly registered with the Corporate Affairs Commission as "PRIMEDGE TECHNOLOGY". This site runs on Secure Sockets Layer (SSL), therefore all transactions on this site are HIGHLY secure and safe!