eChapters

Castration means removal of the testicles and there are two methods of castration in domestic animals viz. closed and open method.

1. Closed method

In closed method, without incision, the spermatic cord is crushed where thrombus is formed which arrest blood flow to the testicles resulting in gradual atrophy of the testicles. ex. Burdizzo method

(A) Anatomy of Lens

The lens is anoptically clear, avascular, biconvex structure of crystalline appearance with an anterior surfaceless curved than the posterior surface, placed between the iris and the vitreous. It is suspended by the suspensory ligament of the lens which is attached to the ciliary body and equator of the lens.

The lens consists of a central nucleus surrounded by the lens fibres and anterior epithelium, encapsulated in an elastic lens capsule. The anterior surface of the lens is in contact with the posterior surface of the iris whereas posterior surface is in contact with the vitreous. As the adult lens does not have a blood supply, its metabolic needs are met by the aqueous humour. The lens is composed of 65% water, 35% protein with scant amounts of electrolytes. The proteins can besubdivided into soluble proteins,

Livestock feeds have a variety of feed stuffs for feeding. Composition and characteristics differ even amongcloselyrelated feeds.Also, cost and availability of such feeds at a particular place, makes the farmer to choose for practical feeding. Therefore, it becomes imperative to learn about such classes. Feeds may generally be classified according to the amount of a specific nutrient they provide intheration. Theymayconvenientlybe divided intotwo general classes– roughages and concentrates. Roughages are bulky feeds containing more than 18 per cent crude fibre, but less than 60 per cent total digestible nutrients. Contrary to this, concentrates have less than 18 per cent fibre, but more than 60 per cent total digestible nutrients. Roughages may be further sub-divided intosucculent and drytypes.Whereas, concentratesare sub-dividedintoEnergy or basal feeds havingless than 20 percent crude protein and Protein supplements havingmorethan 20percent crude protein. Followingfeeds indicate theoutlines of classification [Flow chart 1] of the conventional feeds into broad categories with examples.

Phytochemicals are the individual chemicals from which the plants are made. Phytochemical is simply a word that means plant chemicals. Plants have the ability to synthesize mixtures of structurally diverse bioactive compounds with multiple and mutually potential therapeutic effects. The plants have the capacity of manufacturing the secondary products. Phytochemicals with antioxidant properties tend to be brightly colored because they contain chromophores, ie, a series of alternating single-bonded and double-bonded carbons. Isoprene is often the building block of such units. The darkest green vegetables contain the most chlorophyll, and vegetables with the most chlorophyll require the most antioxidants.

Catheterization is done for both diagnostic as well as therapeutic purpose. As a diagnostic technique it is employed to collect urine samples, prostatic wash and suction biopsy. As a therapeutic technique it is used for the treatment of urine retention, obstruction and for monitoring urine output. Pneumocystography is a contrast radiography. It is being employed to distinguish the urinary bladder from other organs and to visualize the details of the bladder.

Catheterization

An appropriate catheter needs to be selected as per the requirement (purpose of catheterization and duration of catheterization). A soft, silicone flexible catheter is appropriate for indwelling purpose. Whereas a rigid catheter is more desirable to unblock a small calculi and collecting samples for diagnostic purpose. Small size catheters are best in order to minimize urethral trauma.

Important features

• Cattle produce 81% of world milk production, followed by buffaloes with 15 percent, goats with 2 percent and sheep with 1 percent; camels provide 0.5 percent. The remaining share is produced by other dairy species such as equines and yaks.

• About one-third of milk production in developing countries comes from buffaloes, goats, camels and sheep. In developed countries, almost all milk is produced by cattle.

• Milk from dairy species other than cattle represents 40 percent of milk production in Asia, 23 percent in Africa, 3 percent in Europe and 0.5 percent in the Americas; it is almost non-existent in Oceania (FAO)

Taxonomy of Cattle

Cattle belong to the kingdom Animalia, phylum Chordata, class Mammalia, order Artiodactyla, family Bovidae, genus Bos, and species taurus or indicus. Cattle were originally identified by Carolus Linnaeus as three separate species: Bos taurus, Bos indicus, and Bos primigenius. Bovines, which include cattle, bison, African buffalo, water buffalos, and certain antelopes, belong to the subfamily Bovinae.

The caudal vena cava is a large unpaired vein which receives blood from the pelvis, pelvic limbs, mammary glands (in females) and scrotum (in males), the abdominal walls, and the viscera of the abdomen and pelvis. It is formed under the body of the fifth or sixth lumbar vertebra by the union of two common iliac veins which in their turn are formed by the union of the internal iliac and external iliac veins of the corresponding side. It passes cranially in the sublumbar region lying slightly to the right of the median plane and to the right of the abdominal aorta. In the cranial part of the abdomen, it follows the abdominal surface of the diaphragm and is embedded in the liver prior to its entry into the thorax through the foramen vena cava in the diaphragm.

In its abdominal course, the caudal vena cava is related dorsally to the sublumbar muscles and right crus of the diaphragm, ventrally to the colon, pancreas and the liver, on its right to the right kidney and the right adrenal and on its left to the abdominal part of the aorta.

Tributaries of caudal vena cava

The common iliac veins are short vessels formed by the union of the internal and the external iliac veins. These are located at the level of the fifth or sixth lumbar vertebra. The left vein crosses the dorsal surface of the aorta to reach the vena cava.

Key words : CAVD, Drug Design, Bioinformatics, CADD, Co-factor, Vaccinology, infectious diseases, Jenner, immunity, Molecular modeling, Immunoinformatics, Antigen, Antibody, Live Vaccine, Alive Vaccine, Protein-peptide, Enzyme, Tools for Vaccine design,
 
Vaccine – Prevention is Better than Cure

A vaccine is a biological preparation that improves immunity to a particular disease. A vaccine typically contains an agent that resembles a disease-causing microorganism, and is often made from weakened or killed forms of the microbe, its toxins or one of its surface proteins. The agent stimulates the body’s immune system to recognize the agent

1. Introduction
Animal experimentation remains a cornerstone of scientific research in many fields, from medical advances to pharmaceutical testing. However, the ethical treatment of laboratory animals has become a point of significant concern worldwide. India, through the Committee for the Control and Supervision of Experiments on Animals (CCSEA), ensures that ethical standards are maintained in research institutions. Established under the Ministry of Environment, Forests, and Climate Change (MoEF&CC), CCSEA is tasked with overseeing the use of animals in experiments, ensuring that procedures adhere to ethical guidelines and international norms. CCSEA’s guidelines are in line with international standards set forth by organizations such as the International Council for Laboratory Animal Science (ICLAS) and the European Union (EU), but they are tailored to address local needs and conditions. The guidelines, which focus on the welfare of laboratory animals, emphasize the ethical review process, animal care, and the importance of minimizing animal suffering. They also stress the need for researchers to implement the 3Rs—Replacement, Reduction, and Refinement—to minimize the use of animals and ensure humane practices in research. This chapter explores the CCSEA guidelines in detail and compares them with animal welfare regulations from around the world, including the United States, European Union, Japan, and Australia. By understanding the similarities and differences between these regulations, researchers and policymakers can ensure the ethical treatment of laboratory animals on a global scale.
2. Objectives of CCSEA Guidelines
The main objective of the CCSEA guidelines is to ensure that laboratory animals are treated ethically and humanely while also supporting the validity and scientific rigor of research. The guidelines encourage researchers to prioritize animal welfare while minimizing unnecessary suffering. Specifically, CCSEA focuses on:
1. Ethical Treatment of Animals: Ensuring that animals are housed in suitable conditions, given adequate veterinary care, and provided with a comfortable environment to reduce stress.
2. Justification of Animal Use: Ensuring that animals are used only when necessary, and that their use is scientifically justified.
3. Pain and Stress Minimization: Ensuring that experimental procedures cause the least pain, distress and suffering possible.

Dr. Chauhan is an exceptional individual who had achieved a significant milestone in his academic and professional journey. Completing a Bachelor of Science (Honours) with an impressive 80.3%, Dr. Chauhan’s accomplishment is a reflection of his hard work, dedication, and unyielding passion for the field of veterinary science. This remarkable achievement not only underscores his
academic brilliance but also cements his position as an inspiring figure in the veterinary community.
From an early age, Dr. Chauhan demonstrated an innate love for animals and a deep sense of responsibility toward their well-being. These qualities formed the foundation of his journey in veterinary science. His BVSc&AH (Honours) degree, completed with such distinction, is not just a testament to his intellectual capabilities but also to his tireless commitment to improving animal health and welfare. Pursuing a degree in Veterinary science is no small feat. It demands a unique combination of scientific expertise, practical skills, and emotional resilience. For Dr. Chauhan, the rigorous academic journey involved mastering a wide array of subjects, including animal Anatomy, Physiology, Pathology, Pharmacology, and Microbiology. Each subject posed its own set of challenges, yet he tackled them with unwavering determination and an insatiable thirst for knowledge. His exemplary performance, as evidenced by his impressive score of 80.3%, highlights his ability to excel even under pressure. What sets Dr. Chauhan apart is not just his academic excellence but also his holistic approach to learning. Beyond textbooks and lectures, he actively sought opportunities to gain hands-on experience, volunteering at animal shelters and participating in community outreach programs. These experiences not only enriched his understanding of animal care but also shaped his perspective as a compassionate and empathetic veterinary professional.

The cell number of a particular cell type in a total cell population might indicate the physiological or pathological status of the cell smear/FNAC/tissue. ImageJ is a powerful open- source software extensively used for image assessment, including cell counting. In this chapter, the steps to count cells using ImageJ has been discussed. There are two ways to count the cells in a research image using ImageJ.
A. Manual Counting
Use the “Cell Counter” plugin or simply use the multipoint tool in ImageJ. Open it, select the cell type you want to count, and click on each cell in the image to tally them. Double-click on the multipoint tool. A separate window will open named point tool. One can select the type of marking, color and size of making (Figure 30). Keep clicking on the cell type to be counted. It will record the number of cells counted. If one wants to count the second cell type in the same image, change the counter number and select the size, color and type of click point.

A finite growth capacity is a characteristic of all cells derived form the normal animal tissue. The cells pass through a series of age related changes before being incapable to divide further. The finite number of generations of growth is a characteristic of the cell type, age and species of origin and referred to as the “Hayflick limit”. The cells derived from embryonic tissue have a greater growth capacity than those derived from adult tissue.

Introduction

Cell culture is a technique that involves the isolation and in vitro maintenance of cells isolated from tissues or whole organs derived from animals, microbes or plants. This technique has immeasurable role in the field of biology. The scientific progress in biology, microbiology and biotechnology in recent years can be credited on the development of cell culture technology. With the development of cell culture the isolation of viruses has become less cumbersome, the assessment of the efficacy and toxicity of new drugs has been easier, new vaccines are being developed and there has been development in biotechnology assisted reproductive technology.

In general, animal cells have more complex nutritional requirements and usually need more stringent conditions for growth and maintenance. For the growth of the cell in vitro specific mediums are required by the cells. Previously natural mediums like plasma ,serums were used but with the advent of synthetic media the specific needs of different cell types can be catered with. Cell culture is governed by a provided set of protocols requiring a sterile pure culture of cells, various nutrients for its growth, sterile cell culture hood, appropriate aseptic techniques and the utilisation of suitable conditions for optimal viable growth of cells.

Introduction
It is a fundamental biological process in which one cell splits into two or more daughter cells. Both unicellular and multicellular organisms rely heavily on it for growth, development, repair, and reproduction. There are two main types of cell division: mitosis and meiosis. Mitosis occurs in somatic cells and produces two genetically identical daughter cells that share the same chromosomal number as the parent cell. This process is necessary for tissue development and repair. Meiosis, on the other hand, happens in germ cells and results in the formation of gametes, which reduces the number of chromosomes by half to ensure genetic diversity in progeny. Proper regulation of cell division is vital for maintaining cellular health, and disruptions in this process can lead to disorders like cancer.
The different stages of cell division is as follows:-
1. Interphase
• Although not a component of mitosis, interphase is essential for preparing the cell for division. It is separated into three sub-phases:
• G1 phase (Gap 1): The cell expands in size while creating proteins and organelles. S phase (Synthesis): DNA replication occurs, guaranteeing that each daughter cell receives an identical copy of the genetic information.
• G2 phase (Gap 2): The cell continues to expand while new organelles are synthesised)
The cell checks for DNA replication mistakes and gets ready for mitosis.
2. Prophase
• In this phase chromatin condenses into visible chromosomes, each made up of two sister chromatids linked at the centromere.
• The nuclear membrane breaks down, allowing the spindle fibres to interact with the chromosomes.

There are a number of different cell lines derived from human and animals. With the dramatic increase in numbers of cell lines, the risk of intraspecies and interspecies cross contamination rises proportionally. It is particularly a major problem in laboratories where many different cell lines of human and animal origin are handled at a time. The purity of the primary cell or continuous cell lines and species of its origin should be checked on a regular basis to authenticate the cell line identity. In the absence of such monitoring, inter and intra species cell line contamination are likely to occur in the laboratory resulting in loss of investigator’s time effort and resources. The advantages of working with a well defined cell line free from contaminating organisms would appear obvious.

Cell Lysis Procedure

Pellet the cells in a microfuge tube: add 1.5 ml culture, centrifuge for 15 seconds at maximum speed, discard the supernatant, and then repeat the procedure. This will result in the cells from 3 ml of culture in a single tube.

Resuspend the cells in 1 ml Lysis buffer.

Take 300 µl aliquot for Bradford protein assay.

Add 50 µl lysozyme, and mix gently.

After 10-20 minutes at room temperature, microfuge for 10 minutes to pellet cell debris.

Use supernatant for LDH assay.

ALL LIVING ORGANISMS ARE MADE UP OF UNITS CALLED CELLS

All living creatures are made from 1 or more cells

All cells are produced from previously existing cells (no spontaneous generation)

All cells appear to be descended from the first cell which existed about 4 billion years ago

For a species to exist its reproductive cells must be potentially immortal (no aging)

Our bodies start from a single cell and contain about 100,000,000,000,000 (10^14) cells at maturity

Principle

Cell viability refers to the quantity of healthy cells in a sample, while cell proliferation is a crucial indicator for comprehending the mechanisms and pathways involved in the survival of cells or death following exposure to toxic substances. The methods used to assess viability are typically the same as those used to detect cell proliferation. Cell cytotoxicity and proliferation assays are commonly employed in drug evaluations to determine if the test compounds impact cell proliferation or exhibit direct cytotoxic effects. Cell viability can be determined by calculating the ratio of total live cells to the total number of cells (live and dead). Staining also helps to observe the general cell structure. Cell proliferation assay by MTT. Metabolically active cells reduce the yellow tetrazolium MTT (3-(4, 5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium bromide) through dehydrogenase enzymes to produce NADH and NADPH. The purple formazan produced inside the cell can be dissolved and measured using spectrophotometry. The MTT Cell Proliferation Assay quantifies cell proliferation rate and detects decreases in cell viability caused by metabolic events leading to apoptosis or necrosis. The MTT Reagent produces minimal absorbance values when no cells are present.