HAMSTERS

                   BIOLOGY, CARE, DISEASES & MODELS


I.    INTRODUCTION/HISTORY

      A. Approximately 1,000,000 hamsters are used in research
annually in the united states. Of these, 90% are Syrian
(Golden), Mesocrictus auratus, and the remainder are primarily
the Chinese(striped back), Cricetus griseus; the Armenian(gray),
Cricetulus migratorius; and the European, Cricetus cricetus. By
1971, the hamster had become the third most commonly used
laboratory animal in the United States, exceeded only by mice and
rats.

     B. Syrian hamsters, utilized as laboratory animals,
originated from one litter captured in Syria in 1930. Only three
menbers of this litter were retained in captivity, and it is the
progeny of these that were first imported to the United States in
1938. The four main reasons given for selection of the Syrian
Hamster for research are (1) availability and ease of
reproduction,(2) relative freedom from spontaneous diseases
coupled with susceptibility to many introduced pathogenic agents,
(3) anatomical and physiological features with unique potential
for study, and (4) rapid development with short life cycles.

     C. The Chinese hamster was first used as a laboratory
animal in 1949. Since that time it has been used in several
aspects of infectious disease,radiobiological,endocrine,
carcinogenic, and mutagenic research. Since the Chinese hamster
has the lowest chromosome number of any other placental nurtured
lab animal it is useful for cytogenesis research.

     D. The European hamster developed some laboratory
importance when several wild animals caught in a West German
industrial area were found to have had bronchogenic squamous cell
carcinoma. This hamster has since been found to be susceptible
to N-diethylnitrosamine with the resultant development of
respiratory tumors. It was concluded that the European hamster
is a more suitable model than the Syrian hamster for highly
concentrated and prolonged smoke inhalation studies. Also the
Europeon hamster is much larger than other hamster
species(300-400 gm).

     E. The Armenian hamster was first introduced as a
laboratory animal in 1963. It was selected because of its
susceptibility to mutagenic and carcinogenic agents and for
studying meiosis. Their diploid chromosome number is 22.

II.   SYRIAN HAMSTERS

     A. ORIGIN- The Syrian, hamster is native to the arid,
temperate regions of Southeast Europe and Asia Minor. In their
natural environment, hamsters live in deep tunnels that ensure a
cooler temperature and higher humidity than the general desert
environment.

      B.   GENETICS/ANATOMY

           1.   Taxonomy

           ORDER: Rodentia
              FAMILY: Cricetidae
GENUS: Mesocricetus
          SPECIE: auratus

2.   Common names:       Golden or Syrian hamster,Symbol(SYR)

3.   Strains

      a. Inbred Strain (i.e.,20 or more successive
      generations of brother x sister matings)

            Nomenclature of more common types (All
            developed by Billingham and Silvers at Univ Pa)

             (1) MHA/SsLak -White--pink eyes;Mill Hill
             Albino- susceptible to dental caries
             (2) LSH/SsLak -Brown & white; London School
             of Hygiene
             (3) CB/SsLak -Brown & white; Chester Beatty
             Instutite
             (4) PD4/Lak    -White--pink eyes;
             (5) LHC/Lak    -Cream; Lakeview Hamster Colony

       b.    Outbred Strain

            Nomenclature

             (1)   Lak:LVG(SYR) -Golden Syrian


4.   Genotype- Diploid (2N) chromosome number:       44

5. Phenotypic Characteristics- The adult Syrian
hamster is larger than a mouse, usually growing to 6 to
8 inches in length and weighing from 110 to 140 gm. It
virtually tailless, and has smooth, short hair. Normal
coloration is reddish-gold, with grayish-white ventral
portion, however, color can range from albino to dark
brown (Other pertinent anatomical features as follows)

       a.    Dentition:

             (1)   Dental formula
                    1 0    0 3
                   I- C- PM- M- = 16
                    1 0    0 3


             (2) Incissors

                   (a)    Erupted at birth

                   (b)    Grow continuously

             (3) Molars

                   (a) Erupted at birth

                   (b) Cuspidate and do not continue to grow

             (4) Dental caries is easily induced by
             altering diet


      b.    Cheek pouches-     Evaginations of the lateral
buccal wall are devoid of glands and lymphatic
             drainage. These sites are priviledged for foreign
             tissue transplant due to this lack of lymph
             drainage.


             c.   Stomach-   Two compartments

                   (a)   Non-glandular-similar to ruminants
                                      -cardia region

                   (b)   Glandulary   -acid
                                      -pyloric region

                   (c) The two compartments are joined by a
                   narrow passageway with the esophagus entering
                   just proximal to the dividing stricture.

             d.   Sebaceous scent glands
                   (a) costovertebral area
                   (b) larger in male than female
                   (c) function controled by androgens
                   (d) thought to serve as olfactory ID marker

             e.   Pulmonary system

                   (a)   Limited numbers of gland in upper airways
                   (b)   Left lung- single lobe
                   (c)   Right lung-3 lobes(apical,middle,caudal)

             f.   Kidney- The renal papilla extends out into the
                  ureter making it possible to collect urine from
                  tubules in a living hamster.

             g.   Mammary Gland- 14-22 mammae.

             h.   External Genitalia/Sexing
                   (a) Males-greater urogenital distance and
                           only one urogenital opening

                   (b)   Females- Separate vaginal,urinary,and
                            anal openings

C.   PHYSIOLOGY

        1.   Neonatal Development

             a.   Teeth present at birth,eyes & ears closed, and
                  pups are hairless.

             b.   Ears open at 4-5 days

             c.   Eyes open at 15 days

             d.   Eat solid food at 7-10 days

             e.   Weaned at 21-28 days

        2.   Normative Data

             PARAMETER                            VALUE


        Adult weight
Male                          85-140 gm
      Female                        95-120 gm
  Life span
      Average                       2 years
      maximum expected              3 years
  Chromosome number (diploid)       44
  Water consumption                 30 ml/day
  Food consumption                  10-15 gm/day (adult)
  Body temperature                  36.2-37.5 C (rectal)
  Heart rate                        280-412/min
  Respiratory frequency             74(33-127)

HEMOTOLOGY
   RBC                              7,500,000/mm
   WBC                              7,600/mm
   Segmented Neutrophils             21.9%
   Non-segmented Neutrophils         8.0%
   Lymphocytes                      73.5%
   Monocyte                         2.5%
   Eosinophils                      1.1%
   Basophils                        1.1%
   3.Reproduction and mating

        PARAMETERS                    VALUE

  Puberty
      Male                          6-8 weeks (90 gm)
      Female                        6-8 weeks (90-100gm)
  Estrous cycle (1)                 4 days
  Estrus        (2)                 6-10 hours(night)
  Gestation     (3)                 15-18 days
  Litter size                       4-12 pups
  Birth weight                      2-3 gm
  Weaning       (4)                 21 days(35-40gm)
  Optimum breeding life             14 months

      FOOTNOTES

  (1) Stage of cycle can be determined by the tenacity
  and opacity of vaginal discharges-- The discharge is
  thick and opaque at the time of and after ovulation.

  (2) Heat generally begins approximately 1-2 hours after
  dusk on the third day of the estrous cycle and
  ovulation is completed 6-10 hours after onset of
  psychic estrus. The female should be placed in the cage
  with the male at the begining of the dark cycle. If
  the female is receptive she will quickly assume a
  lordotic position with hindlegs spread and tail erect.
  If copulation does not occur within 5 minutes or if the
  female becomes aggressive, she is removed. If
  copulation occurs, the pair can be left together until
  the following light cycle. (3) A copulation plug will
  be visible for a few hours after copulation. Colony
  raised females can be returned to the colony until day
  14 of gestation if they don't fight. Pregnant animals
  should be separated and undisturbed for at least 2 days
  prior to and 7 day after parturition to avoid litter
  cannibolism.

  (4) Estrous cycle will not resume for the mother until
  a few days after her young are weaned. Young from
  different litters can usually be housed together until
  50 days of age.
4.   Behavior

          a. Docile unless surprised or awaken.
          b. Nocturnal                               o
          c. Hibernate when temperature drops below 5 C,
          however, animal is responsive to external stimuli.
          d. Curious by nature

D.   COLONY CARE & HUSBANDRY

     1.   Housing

          a.   Caging
               (1) Plastic shoebox solid bottoms/latchable
               lid to prevent excape.

               (2)   Space   requirements
                      (a)    Hamster < 60gm - 10sq.in.
                      (b)    Hamster > 60gm - 11/20 sq.in.
                      (c)    Female with litter - 150 sq.in.

          b.   Bedding
               (1) Routine types include: hardwood chips,
               sawdust, shavings, corn cobs, and beet pulp.

               (2) Pregnant animals will use soft paper for
               nest building.

               (3) Bedding should be replaced 1 or 2 times
               weekly and can be left as long as 2 weeks when
               is is desirable to leave a litter undisturbed.

          c.   Temperature/Relative Humidity
               (1) Adults should be maintained at
               approximately 65 to 70 degrees F with 40-60%
               relative humidity.

               (2) Breeding rooms should be kept slightly
               warmer (71-75 degrees F).

               (3) Hamsters are more adaptable to cold
               extremes than to warm extremes.


          d.   Photoperiod: 12-14 hour light period daily
               with 14 hours required for breeding colonies.

  2.      Feeding

          a.   Nutritional requirements: Since the hamster's
               first stage of digestion is a fermentation
               process their nutrient utilization is slightly
               different than that of other rodents. Often
               times rat feed is used as a basic diet and is
               then supplemented with rabbit chow or other
               similar diets.

               (1) Soybean meal provides a better protein
               supplement than fishmeal at about 16% of the
               ration. Protein levels of 18-24% promote more
               rapid growth, but at the cost of higher
               incidences of nephritis.
(2) More complex carbohydrates,such as, corn
          starch are more highly tolerated energy
          sources. 30-40% corn starch in the ration is
          ideal

          (3) Compared to the rat, the hamster has a
          higher requirement for zinc, copper, and
          potassium.

     b.   Feed delivery- If food hoppers are used, the
          feed pellets must be able to fall through the
          slots to the floor of the cage. This is
          required because the hamster's muzzle is so
          broad as they would be forced to chew food from
          both sides of the metal strips of the feeder
          resulting in broken teeth and starvation.

     c.   Water- A continuous supply of fresh clean
          water is required. Water delivered via
          Stainless steel siper tubes is most desirable.

3.   Handling

     a. Physical restraint- Insure that the hamster is
     aware of your presence and is not asleep.

          (1) Container or cupped palms are often
          adequate for transfer or weighing.

          (2) One-hand hold (thumb and 3rd finger around
          the thorax stablizing the hindquarters with the
          1st & 2nd fingers.)

     b.   Chemical restraint/preanesthesia/anesthesia

     AGENT                      DOSAGE

     Ketamine HCL               40-150mg/kg IM
                                100-200mg/kg IP
     Xylazine(with ketamine)    10mg/kg IM Improves
                                degree of relaxation

     Pentobarbital(10mg/ml)     50-90mg/kg IP
     Pentobarbital(60mg/ml)     90mg/kg IP
                                30mg/kg IV

     Thiopental                 20mg/kg   IV

     Morphine                   up to 150mg/kg IM;IP;SC
                                analgesia w/o narcosis

     Inhalant anesthetics       cone;chamber;mask

     Atropine sulfate           0.2-0.5mg/kg SC

     c.   IV injection site:   saphenous vein


     d.   Common bleeding sites:

          (1)   Cardiac puncture (requires anesthesia
                2 ml/100gm animal safely)

          (2)   Tail clip (no anesthesia,small quantities)
(3)   Orbital sinus (requires anesthesia,small
                    quantities)

         e.   Euthanasia

              (1)   Physical methods

                     (a)   Cervical dislocation

                     (b)   Decapitation

              (2)   Parenteral methods

                     (a)   Pentobarbital    135-150mg/kg IV
                           minimum

                     (b)   T-61 : not to be used when histo-
                           pathology is anticipated.

              (3)   Inhalant methods

                     (a)   Carbon dioxide

                     (b)   Halothane

                     (c)   Methoxyflurane

                     (d)   Ether(explosive)


E.   SPONTANEOUS DISEASES

     1. Hamsters are generally very resistant to diseases
     and have few health care problems. This, coupled with
     the fact that diseases can be readily induced, make the
     hamster ideal as a model for many human diseases. Some
     disease conditions have been propagated by inbreeding
     to maintain specific models for human disease which are
     not common for the species as a whole.

     2. Common diseases listed in decending order of
     occurrance (below)

         a.   Enteritis

         b.   Pneumonia

         c.   Neoplasia

         d.   Amyloidosis (old animals)

         e.   Polycystic disease

     3. Enteritis is the most common type of spontaneous
     hamster disease. The condition may occur due to a
     broad number of factors from infectious agents to
     management practices.

         a. Common names- Wet tail, proliferative ileitis,
         regional enteritis, and ileal hyperplasia.

         b.   Agents routinely associated with disease.
(1) Clostridium difficile is often isolated
     subsequent to enteric disease associated with
     antibiotic therapy(i.e. clindamycin ampicillin,
     lincomycin) which could indicate that this
     bacterium may play some role in the
     pathogenisis.

     (2) Campylobacter Fetus ssp jejuni has been
     incriminated of late as having a contributing
     role in the clinical symptoms of enteric
     disease. Although it is cultured on occassion
     from clinically normal animals it was reported
     by Lentsch in almost 100% of the hamsters with
     symptoms of proliferative ileopathy.

c.   Predisposing factors

     (1)   Young age.

     (2) Stress (shipping overcrowding lack of
     fresh water.)

     (3)   Poor diet.

     (4)   Antibiotic therapy.

d.   Clinical signs

     (1) Acute - lethargy, anorexia, ruffled hair
     diarrhea, dehydration, and death within 48
     hours. Intussuceptions may occur.

     (2) Subacute-diarrhea, retarded growth and
     eventual death.

     (3) Chronic-palpable abdominal masses with
     emaciation or even normal appearance with
     occassional deaths.

e.   Histopathology - Hyperplasia of the ileal
     absorptive epithelium is the primary lesion.

f.   Treatment - Erythromycin 20mg/kg is most
     desirable.

g.   Differential diagnosis.

     (1) Salmonella spp.- rare spontaneous disease
     of hamster; Dx culture.

     (2)   Tyzers

            (a) Clinical signs may include all those
            listed in regards to proliferative
            ileitis or animals may just be found
            dead.

            (b)   Etiology - Bacillus piliformis.

            (c)   Transmission fecal - oral.

            (d) Pathology - focal necrosis of
            viseral organs.
(e) Diagnosis - tissue smears (silver,
                  PAS or Giemsa stains.)

4    Pneumonias

      a. Clinical signs - depression, anorexia, nasal
      and ocular discharges, respiratory distress and
      chattering.

      b.   Common eitiologies.

           (1)   Pasteurella pneumotropica.

           (2)   Streptococcus spp.

           (3)   Streptococcus pneumoniae.

      c.   Control/Treatment - eleminate stress,
           depopulate or treat with an effective
           antibiotic which does not cause fatal
           enterocolitis.

5.    Neoplasia.

      a. Malignant tumors in (decreasing order of
      ocurrance.

           (1)   Lymphosarcoma.

                  (a) Horizontally transmitted - no type
                  C or retrovirus identified.

                  (b) Epidemic outbreaks in various
                  breeding colonies have reach 50 -90%
                  mortality.

                  (c) Clinical signs - solid tumors
                  enteritis, pyelonephritis, warts, poor
                  breeding efficiency and intussusceptions.

           (2)   Reticulum cell sarcoma - lymphnodes.

           (3)   Carcinoma - intestines and adrenals.

      b.   Benign tumors (most common).

           (1)   Gastro - intestinal polyps.

           (2)   Adenomas of adrenal cortex.

6.    Amyloidosis - principle cause of death in aged
      hamsters. The incidence can reach or exceed 85% in
      hamsters over 18 months of age: The kidney is the
      most likely site of deposition, however, other
      organs are often involved. The disease compares
      with the nephotic syndrome described in humans.

7.    Polycystic Disease - cyst occur in a high incidence
      in hamsters over 1 year of age with the site most
      frequently in the liver. The lesions generally are
      of no clinical significants and are thought to be
      due to developmental defects of ductal structures.

8.    Spontaneous viral diseases
a. Clinical symptoms secondary to common rodent
                 virus (i.e. Sendae,LCM) are rare,however,
                 sero-conversion is common.

                 b. Even though little disease is noted in the
                 hamster lymphocytic choriomeningitis is important
                 because of it's zoonotic implications in humans.
            9.   Spontaneous parasitic diseases

                 a.    Internal

                        (1) Protozoan- Several have been identified
                        but they have little clinical significants.

                        (2)   Nematodes
                                 Syphacia obvelata(mouse pin-worm)
                                 Syphacia muris (rat pin-worm)

                        (3)Helminth
                             (a) Hymenolopsis nana (zoonotic)
                             (b) Hymenolopsis diminuta
                             (c) Can cause obstruction and enteritis

                        (4)   Dx- Fecal exam

                 b.    External

                        (1)   Ornithonyssus bacotis(tropical rat mite)

                        (2)   Notoedres spp.(ear mite)

                        (3)   Demodex criceti
                                   D. aurata-more pathogenic

                        (4)   Dx-Skin scraping


III.    CHINESE HAMSTER

     A. Native to the Eastern shore of China near the Caspian
Sea. They were first successfully bred in 1958, after
illumination schedules were reversed.

       B.   Taxonomy

            ORDER: Rodentia
               FAMILY: Cricetidae
                  GENUS: Cricetus
                     SPECIE: griseus

       C.   Physiology

            1.   Mayor differences from Syrian hamsters

            PARAMETER                             VALUE

            Chromosome(2N)                        22

            Adult Weight                          39-46 gm

            Body Length                           4 inches

            Water Intake                          11-13 ml/100gm
2.   Reproductive physiology

      PARAMETER                         VALUE
      _______________________________________________________

      Incisors                            Erupted at birth

      Eyes & ears open                    10-14 days

      Weaned                              21-25 days

      Sexually mature                     8-12 weeks

      Estrous cycle                       Polyestrus

      Estrous cycle duration              4 days

      Estrus                              6-8 hours

      Ovulation time                      Just before estrus

      Copulation                          2-4 hours after start
                                              of dark period

      Implantation                        5-6 days

      Gestation                           20.5 days

      Average litter size                 4-5

      Mammae numbers                      8

      Postpartum estrus                   4 days

      _______________________________________________________


      2.   Hemogram similar to Syrian hamster


D.    Diseases

      1.   Very few spontaneous infectious diseases reported.

      2.   Metabolic

           a.    Diabetes mellitus

                  (1) insulin dependent
                  (2) similar to human
                  (3) clinical signs-polydypsia,polyuria,
                  dehydration, blindness and death especially
                  after stress
                  (4) recessive factor-propogated by inbreeding

      3.   Neoplasia-low incidence

      4.   Miscellaneous

           a. Periodontitis-Epecially in those with diabetes
           which resembles the same condition in humans with
           diabetes.
b.   Nephrosclerosis

                 c. Spondylosis-     Higher incidence in hamsters with
                 diabetes.

IV.    EXPERIMENTAL MODELS/USES

      A.   Spontaneous Models of Human Disease

           1. Diabetes mellitus in the Chinese hamster was
           recognized in 1957. The disease is associated with a
           decrease of the pancreatic B cells. It is insulin
           dependent, juvinile onset,and hypoinsulinemic similar to
           the juvinile type in man.

           2.   Syrian hamster dystrophy

                 a.   strains:   BIO 1.50-original strain
                                 BI0 4.6 -acromelanic,homozygous
                                     affected
                                 BIO 50.54-agoute,homozygous affected
                                 BIO 82.62-acromelanic,homozygous
                                     affected
                                 BIO 53.58-homozygous affected

                 b. Autosomal recessive skeletal muscle
                 degeneration

                 c. Serum levels of phosphocreatine kinase parallel
                 the course of the disease and calcific tongue
                 lesions are pathognomonic of the disease.

                 d. also develop cardiomyopathy,
                 cardiohypertrophy, and congestive heart
                 failure-die by nine months of age

           Comparison: Good model for physiology and pathogenesis
           of Duchenne's dystrophy: variable size

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laboratory animals handling and storage.pptx

Hamstbio

  • 1. HAMSTERS BIOLOGY, CARE, DISEASES & MODELS I. INTRODUCTION/HISTORY A. Approximately 1,000,000 hamsters are used in research annually in the united states. Of these, 90% are Syrian (Golden), Mesocrictus auratus, and the remainder are primarily the Chinese(striped back), Cricetus griseus; the Armenian(gray), Cricetulus migratorius; and the European, Cricetus cricetus. By 1971, the hamster had become the third most commonly used laboratory animal in the United States, exceeded only by mice and rats. B. Syrian hamsters, utilized as laboratory animals, originated from one litter captured in Syria in 1930. Only three menbers of this litter were retained in captivity, and it is the progeny of these that were first imported to the United States in 1938. The four main reasons given for selection of the Syrian Hamster for research are (1) availability and ease of reproduction,(2) relative freedom from spontaneous diseases coupled with susceptibility to many introduced pathogenic agents, (3) anatomical and physiological features with unique potential for study, and (4) rapid development with short life cycles. C. The Chinese hamster was first used as a laboratory animal in 1949. Since that time it has been used in several aspects of infectious disease,radiobiological,endocrine, carcinogenic, and mutagenic research. Since the Chinese hamster has the lowest chromosome number of any other placental nurtured lab animal it is useful for cytogenesis research. D. The European hamster developed some laboratory importance when several wild animals caught in a West German industrial area were found to have had bronchogenic squamous cell carcinoma. This hamster has since been found to be susceptible to N-diethylnitrosamine with the resultant development of respiratory tumors. It was concluded that the European hamster is a more suitable model than the Syrian hamster for highly concentrated and prolonged smoke inhalation studies. Also the Europeon hamster is much larger than other hamster species(300-400 gm). E. The Armenian hamster was first introduced as a laboratory animal in 1963. It was selected because of its susceptibility to mutagenic and carcinogenic agents and for studying meiosis. Their diploid chromosome number is 22. II. SYRIAN HAMSTERS A. ORIGIN- The Syrian, hamster is native to the arid, temperate regions of Southeast Europe and Asia Minor. In their natural environment, hamsters live in deep tunnels that ensure a cooler temperature and higher humidity than the general desert environment. B. GENETICS/ANATOMY 1. Taxonomy ORDER: Rodentia FAMILY: Cricetidae
  • 2. GENUS: Mesocricetus SPECIE: auratus 2. Common names: Golden or Syrian hamster,Symbol(SYR) 3. Strains a. Inbred Strain (i.e.,20 or more successive generations of brother x sister matings) Nomenclature of more common types (All developed by Billingham and Silvers at Univ Pa) (1) MHA/SsLak -White--pink eyes;Mill Hill Albino- susceptible to dental caries (2) LSH/SsLak -Brown & white; London School of Hygiene (3) CB/SsLak -Brown & white; Chester Beatty Instutite (4) PD4/Lak -White--pink eyes; (5) LHC/Lak -Cream; Lakeview Hamster Colony b. Outbred Strain Nomenclature (1) Lak:LVG(SYR) -Golden Syrian 4. Genotype- Diploid (2N) chromosome number: 44 5. Phenotypic Characteristics- The adult Syrian hamster is larger than a mouse, usually growing to 6 to 8 inches in length and weighing from 110 to 140 gm. It virtually tailless, and has smooth, short hair. Normal coloration is reddish-gold, with grayish-white ventral portion, however, color can range from albino to dark brown (Other pertinent anatomical features as follows) a. Dentition: (1) Dental formula 1 0 0 3 I- C- PM- M- = 16 1 0 0 3 (2) Incissors (a) Erupted at birth (b) Grow continuously (3) Molars (a) Erupted at birth (b) Cuspidate and do not continue to grow (4) Dental caries is easily induced by altering diet b. Cheek pouches- Evaginations of the lateral
  • 3. buccal wall are devoid of glands and lymphatic drainage. These sites are priviledged for foreign tissue transplant due to this lack of lymph drainage. c. Stomach- Two compartments (a) Non-glandular-similar to ruminants -cardia region (b) Glandulary -acid -pyloric region (c) The two compartments are joined by a narrow passageway with the esophagus entering just proximal to the dividing stricture. d. Sebaceous scent glands (a) costovertebral area (b) larger in male than female (c) function controled by androgens (d) thought to serve as olfactory ID marker e. Pulmonary system (a) Limited numbers of gland in upper airways (b) Left lung- single lobe (c) Right lung-3 lobes(apical,middle,caudal) f. Kidney- The renal papilla extends out into the ureter making it possible to collect urine from tubules in a living hamster. g. Mammary Gland- 14-22 mammae. h. External Genitalia/Sexing (a) Males-greater urogenital distance and only one urogenital opening (b) Females- Separate vaginal,urinary,and anal openings C. PHYSIOLOGY 1. Neonatal Development a. Teeth present at birth,eyes & ears closed, and pups are hairless. b. Ears open at 4-5 days c. Eyes open at 15 days d. Eat solid food at 7-10 days e. Weaned at 21-28 days 2. Normative Data PARAMETER VALUE Adult weight
  • 4. Male 85-140 gm Female 95-120 gm Life span Average 2 years maximum expected 3 years Chromosome number (diploid) 44 Water consumption 30 ml/day Food consumption 10-15 gm/day (adult) Body temperature 36.2-37.5 C (rectal) Heart rate 280-412/min Respiratory frequency 74(33-127) HEMOTOLOGY RBC 7,500,000/mm WBC 7,600/mm Segmented Neutrophils 21.9% Non-segmented Neutrophils 8.0% Lymphocytes 73.5% Monocyte 2.5% Eosinophils 1.1% Basophils 1.1% 3.Reproduction and mating PARAMETERS VALUE Puberty Male 6-8 weeks (90 gm) Female 6-8 weeks (90-100gm) Estrous cycle (1) 4 days Estrus (2) 6-10 hours(night) Gestation (3) 15-18 days Litter size 4-12 pups Birth weight 2-3 gm Weaning (4) 21 days(35-40gm) Optimum breeding life 14 months FOOTNOTES (1) Stage of cycle can be determined by the tenacity and opacity of vaginal discharges-- The discharge is thick and opaque at the time of and after ovulation. (2) Heat generally begins approximately 1-2 hours after dusk on the third day of the estrous cycle and ovulation is completed 6-10 hours after onset of psychic estrus. The female should be placed in the cage with the male at the begining of the dark cycle. If the female is receptive she will quickly assume a lordotic position with hindlegs spread and tail erect. If copulation does not occur within 5 minutes or if the female becomes aggressive, she is removed. If copulation occurs, the pair can be left together until the following light cycle. (3) A copulation plug will be visible for a few hours after copulation. Colony raised females can be returned to the colony until day 14 of gestation if they don't fight. Pregnant animals should be separated and undisturbed for at least 2 days prior to and 7 day after parturition to avoid litter cannibolism. (4) Estrous cycle will not resume for the mother until a few days after her young are weaned. Young from different litters can usually be housed together until 50 days of age.
  • 5. 4. Behavior a. Docile unless surprised or awaken. b. Nocturnal o c. Hibernate when temperature drops below 5 C, however, animal is responsive to external stimuli. d. Curious by nature D. COLONY CARE & HUSBANDRY 1. Housing a. Caging (1) Plastic shoebox solid bottoms/latchable lid to prevent excape. (2) Space requirements (a) Hamster < 60gm - 10sq.in. (b) Hamster > 60gm - 11/20 sq.in. (c) Female with litter - 150 sq.in. b. Bedding (1) Routine types include: hardwood chips, sawdust, shavings, corn cobs, and beet pulp. (2) Pregnant animals will use soft paper for nest building. (3) Bedding should be replaced 1 or 2 times weekly and can be left as long as 2 weeks when is is desirable to leave a litter undisturbed. c. Temperature/Relative Humidity (1) Adults should be maintained at approximately 65 to 70 degrees F with 40-60% relative humidity. (2) Breeding rooms should be kept slightly warmer (71-75 degrees F). (3) Hamsters are more adaptable to cold extremes than to warm extremes. d. Photoperiod: 12-14 hour light period daily with 14 hours required for breeding colonies. 2. Feeding a. Nutritional requirements: Since the hamster's first stage of digestion is a fermentation process their nutrient utilization is slightly different than that of other rodents. Often times rat feed is used as a basic diet and is then supplemented with rabbit chow or other similar diets. (1) Soybean meal provides a better protein supplement than fishmeal at about 16% of the ration. Protein levels of 18-24% promote more rapid growth, but at the cost of higher incidences of nephritis.
  • 6. (2) More complex carbohydrates,such as, corn starch are more highly tolerated energy sources. 30-40% corn starch in the ration is ideal (3) Compared to the rat, the hamster has a higher requirement for zinc, copper, and potassium. b. Feed delivery- If food hoppers are used, the feed pellets must be able to fall through the slots to the floor of the cage. This is required because the hamster's muzzle is so broad as they would be forced to chew food from both sides of the metal strips of the feeder resulting in broken teeth and starvation. c. Water- A continuous supply of fresh clean water is required. Water delivered via Stainless steel siper tubes is most desirable. 3. Handling a. Physical restraint- Insure that the hamster is aware of your presence and is not asleep. (1) Container or cupped palms are often adequate for transfer or weighing. (2) One-hand hold (thumb and 3rd finger around the thorax stablizing the hindquarters with the 1st & 2nd fingers.) b. Chemical restraint/preanesthesia/anesthesia AGENT DOSAGE Ketamine HCL 40-150mg/kg IM 100-200mg/kg IP Xylazine(with ketamine) 10mg/kg IM Improves degree of relaxation Pentobarbital(10mg/ml) 50-90mg/kg IP Pentobarbital(60mg/ml) 90mg/kg IP 30mg/kg IV Thiopental 20mg/kg IV Morphine up to 150mg/kg IM;IP;SC analgesia w/o narcosis Inhalant anesthetics cone;chamber;mask Atropine sulfate 0.2-0.5mg/kg SC c. IV injection site: saphenous vein d. Common bleeding sites: (1) Cardiac puncture (requires anesthesia 2 ml/100gm animal safely) (2) Tail clip (no anesthesia,small quantities)
  • 7. (3) Orbital sinus (requires anesthesia,small quantities) e. Euthanasia (1) Physical methods (a) Cervical dislocation (b) Decapitation (2) Parenteral methods (a) Pentobarbital 135-150mg/kg IV minimum (b) T-61 : not to be used when histo- pathology is anticipated. (3) Inhalant methods (a) Carbon dioxide (b) Halothane (c) Methoxyflurane (d) Ether(explosive) E. SPONTANEOUS DISEASES 1. Hamsters are generally very resistant to diseases and have few health care problems. This, coupled with the fact that diseases can be readily induced, make the hamster ideal as a model for many human diseases. Some disease conditions have been propagated by inbreeding to maintain specific models for human disease which are not common for the species as a whole. 2. Common diseases listed in decending order of occurrance (below) a. Enteritis b. Pneumonia c. Neoplasia d. Amyloidosis (old animals) e. Polycystic disease 3. Enteritis is the most common type of spontaneous hamster disease. The condition may occur due to a broad number of factors from infectious agents to management practices. a. Common names- Wet tail, proliferative ileitis, regional enteritis, and ileal hyperplasia. b. Agents routinely associated with disease.
  • 8. (1) Clostridium difficile is often isolated subsequent to enteric disease associated with antibiotic therapy(i.e. clindamycin ampicillin, lincomycin) which could indicate that this bacterium may play some role in the pathogenisis. (2) Campylobacter Fetus ssp jejuni has been incriminated of late as having a contributing role in the clinical symptoms of enteric disease. Although it is cultured on occassion from clinically normal animals it was reported by Lentsch in almost 100% of the hamsters with symptoms of proliferative ileopathy. c. Predisposing factors (1) Young age. (2) Stress (shipping overcrowding lack of fresh water.) (3) Poor diet. (4) Antibiotic therapy. d. Clinical signs (1) Acute - lethargy, anorexia, ruffled hair diarrhea, dehydration, and death within 48 hours. Intussuceptions may occur. (2) Subacute-diarrhea, retarded growth and eventual death. (3) Chronic-palpable abdominal masses with emaciation or even normal appearance with occassional deaths. e. Histopathology - Hyperplasia of the ileal absorptive epithelium is the primary lesion. f. Treatment - Erythromycin 20mg/kg is most desirable. g. Differential diagnosis. (1) Salmonella spp.- rare spontaneous disease of hamster; Dx culture. (2) Tyzers (a) Clinical signs may include all those listed in regards to proliferative ileitis or animals may just be found dead. (b) Etiology - Bacillus piliformis. (c) Transmission fecal - oral. (d) Pathology - focal necrosis of viseral organs.
  • 9. (e) Diagnosis - tissue smears (silver, PAS or Giemsa stains.) 4 Pneumonias a. Clinical signs - depression, anorexia, nasal and ocular discharges, respiratory distress and chattering. b. Common eitiologies. (1) Pasteurella pneumotropica. (2) Streptococcus spp. (3) Streptococcus pneumoniae. c. Control/Treatment - eleminate stress, depopulate or treat with an effective antibiotic which does not cause fatal enterocolitis. 5. Neoplasia. a. Malignant tumors in (decreasing order of ocurrance. (1) Lymphosarcoma. (a) Horizontally transmitted - no type C or retrovirus identified. (b) Epidemic outbreaks in various breeding colonies have reach 50 -90% mortality. (c) Clinical signs - solid tumors enteritis, pyelonephritis, warts, poor breeding efficiency and intussusceptions. (2) Reticulum cell sarcoma - lymphnodes. (3) Carcinoma - intestines and adrenals. b. Benign tumors (most common). (1) Gastro - intestinal polyps. (2) Adenomas of adrenal cortex. 6. Amyloidosis - principle cause of death in aged hamsters. The incidence can reach or exceed 85% in hamsters over 18 months of age: The kidney is the most likely site of deposition, however, other organs are often involved. The disease compares with the nephotic syndrome described in humans. 7. Polycystic Disease - cyst occur in a high incidence in hamsters over 1 year of age with the site most frequently in the liver. The lesions generally are of no clinical significants and are thought to be due to developmental defects of ductal structures. 8. Spontaneous viral diseases
  • 10. a. Clinical symptoms secondary to common rodent virus (i.e. Sendae,LCM) are rare,however, sero-conversion is common. b. Even though little disease is noted in the hamster lymphocytic choriomeningitis is important because of it's zoonotic implications in humans. 9. Spontaneous parasitic diseases a. Internal (1) Protozoan- Several have been identified but they have little clinical significants. (2) Nematodes Syphacia obvelata(mouse pin-worm) Syphacia muris (rat pin-worm) (3)Helminth (a) Hymenolopsis nana (zoonotic) (b) Hymenolopsis diminuta (c) Can cause obstruction and enteritis (4) Dx- Fecal exam b. External (1) Ornithonyssus bacotis(tropical rat mite) (2) Notoedres spp.(ear mite) (3) Demodex criceti D. aurata-more pathogenic (4) Dx-Skin scraping III. CHINESE HAMSTER A. Native to the Eastern shore of China near the Caspian Sea. They were first successfully bred in 1958, after illumination schedules were reversed. B. Taxonomy ORDER: Rodentia FAMILY: Cricetidae GENUS: Cricetus SPECIE: griseus C. Physiology 1. Mayor differences from Syrian hamsters PARAMETER VALUE Chromosome(2N) 22 Adult Weight 39-46 gm Body Length 4 inches Water Intake 11-13 ml/100gm
  • 11. 2. Reproductive physiology PARAMETER VALUE _______________________________________________________ Incisors Erupted at birth Eyes & ears open 10-14 days Weaned 21-25 days Sexually mature 8-12 weeks Estrous cycle Polyestrus Estrous cycle duration 4 days Estrus 6-8 hours Ovulation time Just before estrus Copulation 2-4 hours after start of dark period Implantation 5-6 days Gestation 20.5 days Average litter size 4-5 Mammae numbers 8 Postpartum estrus 4 days _______________________________________________________ 2. Hemogram similar to Syrian hamster D. Diseases 1. Very few spontaneous infectious diseases reported. 2. Metabolic a. Diabetes mellitus (1) insulin dependent (2) similar to human (3) clinical signs-polydypsia,polyuria, dehydration, blindness and death especially after stress (4) recessive factor-propogated by inbreeding 3. Neoplasia-low incidence 4. Miscellaneous a. Periodontitis-Epecially in those with diabetes which resembles the same condition in humans with diabetes.
  • 12. b. Nephrosclerosis c. Spondylosis- Higher incidence in hamsters with diabetes. IV. EXPERIMENTAL MODELS/USES A. Spontaneous Models of Human Disease 1. Diabetes mellitus in the Chinese hamster was recognized in 1957. The disease is associated with a decrease of the pancreatic B cells. It is insulin dependent, juvinile onset,and hypoinsulinemic similar to the juvinile type in man. 2. Syrian hamster dystrophy a. strains: BIO 1.50-original strain BI0 4.6 -acromelanic,homozygous affected BIO 50.54-agoute,homozygous affected BIO 82.62-acromelanic,homozygous affected BIO 53.58-homozygous affected b. Autosomal recessive skeletal muscle degeneration c. Serum levels of phosphocreatine kinase parallel the course of the disease and calcific tongue lesions are pathognomonic of the disease. d. also develop cardiomyopathy, cardiohypertrophy, and congestive heart failure-die by nine months of age Comparison: Good model for physiology and pathogenesis of Duchenne's dystrophy: variable size