Basic bio Flashcards

1
Q

Neutrophil extravasation. Leukocyte extravasation is a multistep process orchestrated by both hemostatic and cell–cell interactions. Margination and rolling of leukocytes along the vascular endothelium are mediated through interactions between endothelial selectins with their corresponding leukocyte ligands. Chemokines stimulate increased expression and enhanced binding affinity of leukocyte integrins, leading to firm adherence to endothelial cell integrins (e.g., intracellular adhesion molecule [ICAM]-1). Leukocyte diapedesis is facilitated by the adhesion molecule, platelet–endothelial cell adhesion molecule (PECAM)-1, and leukocytes follow chemokine gradients to the site of injury. IL-1, Interleukin-1; TNF, tumor necrosis factor

A

Proinflammatory response to alarm signals. In response to pathogen-associated molecular patterns (PAMPS) or danger-associated molecular patterns (DAMPS), toll-like receptors (TLRs) on the surface of resident macrophages induce various molecular signaling pathways. Many of these pathways lead to the translocation of nuclear factor kappa B (NFκB) into the cell nucleus, where it acts as a transcription factor, regulating the production of proinflammatory cytokines. The cytokines act directly and indirectly on a number of cell types. Interleukin (IL)-6 induces hepatic production of acute phase proteins, which in turn influence a number of inflammatory systems. Chemokines induce recruitment of inflammatory cells, which produce additional mediators. If the process is not properly balanced by antiinflammatory responses, tissue damage and systemic inflammation may result in serious consequences. CRP, C-reactive protein; NO, nitric oxide; ROS, reactive oxygen species.

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2
Q

The arachidonic acid pathway. Arachidonic acid is metabolized by the cyclooxygenase or lipoxygenase pathway to produce prostaglandins or leukotrienes and proresolution lipoxins, respectively. The inhibitory effects of several drugs on specific enzymes are denoted by a red X. COX, Cyclooxygenase; HETE, hydroxyeicosatetraenoic acid; HPETE, hydroperoxyeicosatetraenoic acid.

A

Cellular Origins and Functions of Prostaglandins

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3
Q

Functions of nitric oxide. Endothelial-derived nitric oxide synthase (eNOS) functions to maintain normal vascular tone via the vasodilatory effects of nitric oxide on vascular smooth muscle. In addition, nitric oxide modulates the interactions of platelets and leukocytes with the vascular endothelium. At increased levels, inducible nitric oxide synthase (iNOS) facilitates nitric oxide–derived free radical production and removal of target pathogens by macrophages. NO, Nitric oxide.

A

Complement pathway activation and effector functions. The complement cascade is activated via three different pathways, all of which culminate in cleavage of C3 into C3b and C3a. Complement proteins and breakdown products facilitate several aspects of inflammatory responses as well as pathogen removal via phagocytosis and membrane attack complex (MAC) production

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4
Q

The central dogma of molecular biology. Genomic DNA (gDNA) is transcribed to mRNA, starting at the first exon (E1), after the initiation of transcription. The whole gene sequence, not including the promoter region (P), is transcribed before splicing removes the introns (I). Translation of the mature mRNA sequence produces the protein.

A

The polymerase chain reaction (PCR). RNA or DNA (gDNA, genomic DNA) can be evaluated, but RNA is usually reverse transcribed into complementary DNA (cDNA) before the PCR occurs. First, the sample is heated to separate the DNA into single strands (denatured). The sample is then cooled to allow the primers to bind to their target sequence (annealing). Finally, the mixture temperature is increased to the optimum for DNA polymerase use. The DNA polymerase then synthesizes a new DNA template (extension or elongation). After each PCR cycle, the number of templates is doubled

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5
Q

The polymerase chain reaction (PCR). RNA or DNA (gDNA, genomic DNA) can be evaluated, but RNA is usually reverse transcribed into complementary DNA (cDNA) before the PCR occurs. First, the sample is heated to separate the DNA into single strands (denatured). The sample is then cooled to allow the primers to bind to their target sequence (annealing). Finally, the mixture temperature is increased to the optimum for DNA polymerase use. The DNA polymerase then synthesizes a new DNA template (extension or elongation). After each PCR cycle, the number of templates is doubled

A

Figure 5-1 Total body water (TBW) fluid compartments.

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6
Q

Intracelluar and extracellular compartment % of total body water?

A

Intracellular = 66% total body water and 40% total body weight

Extrecellular 33%, 20% total body weight = plasma 25%, interstital 75%

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7
Q

What is the osmolarity of body fluid compartments?

A

290-310mOsm/L

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8
Q

What precursors are used in fluids as buffer?

A

Lactate - liver to bicarb

Acetate - muscle

Gluconate - cells

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9
Q

What isotonic fluid is “unbalanced” and what happens when this is given as a bolus?

A

0.9% NaCL

mild increase Na, Marked increase Cl, moderated decrease bicarb and K (acidfying effect)

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10
Q

What percent of isotonic fluids (extracellular expanding fluids) are redistributed to the intersitial space?

A

75%

only 25% remain in intravascular space

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11
Q

What are hypotonic fluids?

A
  1. 45% saline
  2. 5% dextrose with 0.45% saline

2.5% dextrose with half strength LRS
Normosol M

Plasmalyte 56

D5W

large volumes can rapidly decrease osmolarity and cause cerebral edema

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12
Q

What are the side effects related to synthetic colloids?

A

decrese factor VIII and vW factor

impairment platelet function

interference in stability of fibrin clots

dose hypoproteinemia = 0.5-2ml/kg/day

shock dose 5-10ml/kg

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13
Q

What are the standard doses for blood products?

A

pRBC and FFP = 10-15ml/kg

whole blood = 20-25ml/kg

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14
Q

What is the formula for blood adminstration based on target PCV?

A

V rbc = blood V x (target PCV- current PCV/ donor PCV)

blood V = 90ml/kg dog and 50ml/kg cat

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15
Q

what is the PCV of packed rbc?

A

80%

lifespan 20-35 d at 4 C

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16
Q

How do you calculate fluid replacement?

A
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17
Q

What is the formula for daily water requirement?

A

FOR CATS: BW(KG)^75 × 80 = ML/DAY

FOR DOGS: BW(KG)^75 × 132 = ML/DAY

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18
Q

Isotonic Crystalloid Compositions?

A
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19
Q

Albumin accounts for what percent % of plasma oncotic pressure?

A

80%

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20
Q

Causes of Hyponatremia

A
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21
Q

Causes of Hypokalemia

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22
Q

Causes of Hyperkalemia

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23
Q

Causes of Hypocalcemia

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24
Q

Box • 5-7 Causes of Hypomagnesemia

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25
Q

What is Wipple’s triad?

A

A low blood glucose concentration with concurrent clinical signs of hypoglycemia, as well as resolution of clinical signs when the blood glucose level is normalized, constitutes a clinical definition of hypoglycemia known as Whipple’s triad

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26
Q

Box • 5-8 Causes of Hypermagnesemia

A

A serum concentration of magnesium greater than 2.51 mg/dL in dogs and greater than 2.99 mg/dL in cats is consistent with hypermagnesemia, but clinical signs are generally seen at levels exceeding 4 mg/dL. Electrocardiographic changes that may occur in patients with hypermagnesemia include prolongation of the PR interval, widening of the QRS complex, and, at higher concentrations, heart block and asystole. Hypermagnesemia may cause hypotension and can interfere with normal clotting and coagulation. Hypermagnesemia also has muscular effects similar to hypercalcemia, including weakness and decreased tendon reflexes.77,78 Treatment of hypermagnesemia includes fluid therapy and administration of loop diuretics (furosemide). Severe cases can be treated with calcium gluconate, as calcium is an antagonist of magnesium at the neuromuscular junction. Anticholinesterases such as physostigmine may also help reduce the actions of magnesium at the neuromuscular junction

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27
Q

Causes of Hypophosphatemia

A
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28
Q

Causes of Hyperphosphatemia

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29
Q

Causes of Corrected Hypochloremia

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30
Q

Causes of Corrected Hyperchloremia

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31
Q

Causes of Hypoglycemia

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32
Q

Causes of Hyperglycemia

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33
Q

Reabsorption of filtered [HCO3−] by H+ secretion in the proximal tubule.

A
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34
Q

Where does the majority of bicarb resorbtion occur?

A

Ninety to 95% of filtered HCO3− is reabsorbed in the proximal tubule, and the rest is reabsorbed in the loop of Henle, distal tubule, and collecting duct.

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35
Q

Table • 5-8 Normal Blood Gas Values in the Dog and Cat (mean ± SD)

A
36
Q

Serum Anion and Cation Concentrations (mEq/L) in the Dog and Cat

A
37
Q

Compensatory Responses to Simple Acid-Base Disturbances in Dogs

A
38
Q

Septic chapter equations

A
39
Q

Box • 6-3 Defects in Oxygen Uptake

A

Diffusional shunting: This is caused by slow blood velocity (prolonged transit time), which favors diffusional oxygen transport over convective oxygen transport (i.e., the movement of oxygen following a concentration gradient prevails over transport of oxygen within the bloodstream). It may occur in the intestine during shock states. The intestine relies on countercurrent blood flow to deliver blood to the villi. If the rate of flow is so slow that oxygen from the arterial blood can diffuse to the venous blood before it is delivered to the tip of the villus, the intestine will be hypoxic, but venous saturation will actually be increased.

Diffusional resistance: For cells to utilize oxygen, O2 must diffuse from the vascular space through the tissues, into the cell, and finally to the mitochondria. Oxygen is poorly soluble in aqueous solutions; therefore tissue edema will increase diffusional distance and limit oxygen availability to the tissues. Hypoxia may increase edema by increasing vascular permeability, thus leading to a “feed-forward” cycle of hypoxia and edema and more hypoxia. Impaired diffusion will result in a smaller gradient, less driving pressure for the oxygen to leave the hemoglobin, and thus higher venous saturation, despite tissue hypoxia. •

Arteriovenous shunting: One of the most obvious reasons for failure of oxygen uptake by the cells is the loss of normal capillary flow. In sepsis, trauma, and diseases associated with systemic activation of the inflammatory response, capillary obstruction can result from neutrophil-endothelial interaction, platelet aggregation, thrombi, or loss of normal vasodilatory function. As a result, arterial blood bypasses the hypoxic bed, leading to an increase in venous oxygen saturation.

Perfusion/metabolism mismatch: A cause of inadequate tissue oxygenation is perfusion/metabolism mismatch. Despite the normal excess (approximately four-fold) of oxygen delivery in relation to tissue demand, in some tissues and in some disease states the increased metabolic demand combined with reduced blood flow can lead to tissue hypoxia. A classic example is sustained tachycardia, when c_oronary perfusion is reduced because of shortened diastole, yet the metabolic demand of the myocytes is increased_.

Cytopathic hypoxia (mitochondrial dysfunction): Cytopathic hypoxia is classically associated with sepsis. Experimental studies of sepsis have demonstrated that despite direct measurement of adequate cellular oxygen, mitochondrial respiration is impaired. Proposed mechanisms to explain this “cytopathic hypoxia” include the following: •Inhibition of pyruvate dehydrogenase and subsequent lactate accumulation •Nitric oxide–mediated inhibition of mitochondrial electron transport •Poly-(ADP-ribosyl)-polymerase activation by reactive oxygen species and subsequent depletion of NAD+/NADH for oxidative phosphorylation

40
Q

What does a CVP <0 and a CVP >10 indicate?

A

<0 = hypovolemic shock

>10 = cardiogenic shock

41
Q

What level of deoxygenated hemoglobin is present in the blood before cyanosis occurs?

A

>5mg/dL

42
Q

Normally what is PaO2 on room air and on 100% O2?

A

Room air >90mmHg

should be 5x inspired O2

O2 toxicity occurs if FiO2>60% for greater than 24 hours

43
Q

Vasoactive and Inotropic Agents—Intravenous Constant Rate Infusion

A
44
Q

SIRS Criteria for Dogs, Cats, and People

A
45
Q

Diagnostic Criteria for Veterinary Acute Respiratory Distress Syndrome (ARDS)

A
46
Q

What is the normal BMBT in the dog and cat?

A

Dog = 1.7 -4.2 min

Cat = 1.4 -2.4 min

Prolonged with thrombocytopenia, thrombopathia and vasculopathy

Affected by hematocrit and blood viscosity

Upto 2min intraoperator variation

47
Q

What is activated clotting time, what pathway does it test and what is it influenced by?

A

Whole blood into 37 C tube with diatomaceous earth (contact activator 12)

Normal clot time dog <100s, normal cat <75s

Less sensative than PTT, influence by thrombocytopenia <15,000, thrombopathia, anemai, blood viscosity, incubation temperature

48
Q

In order for PT, aPTT and ACT to be prolonged, what level is fibrinogen?

A

<50-100 mg/dL

Thrombin clotting time prolonged in hypofibrinogenemia

49
Q

Differential Diagnoses of Prolonged Coagulation Times: Prothrombin Time and Activated Partial Thromboplastin Time

A
50
Q

Differentials thrombocytopenia

A

Diffenertials thrombopathia

51
Q

Disorders secondary hemostatsis

A
52
Q

What is a massive transfusion?

A

Transfusion >patient blood volume (dog 90ml/kg, cat 66ml/kg) in 24 hours

OR

50% within 3 hours

Fibrinogen critically reduced

No clot is formed <50mg/dL livearly up to 300mg/dL

53
Q

What clotting factors does hetastarch influence?

A

fibrinogen, vWF, F8

54
Q

How does temperature affect platelet function?

A

33-37 (98.6F) = Decreased vWB mediated platelet adhesion

<33 C (91F) = decrease platelet function and TF-fVIIa complex activity

55
Q

How does acidemia effect clotting?

A

Increased fibrinogen degredation

impairs coagulation protein activity

F10-F5a complex activity decreased 50% ph 7.2, 70% at ph 7

56
Q

Plasma Component Transfusions

A
57
Q

What is the MOA aminocaproic acid?

A

Lysine analogues, block binding and activation of plasminogen

anti-inflammatory via inhibition of interleukin

Other antifibrinolytics: aprotinin (serine protease, inhibits plasmin), Recombinant factor 7a

58
Q

Platelet Transfusions

A
59
Q

Antithrombotic Drugs: Preoperative Discontinuation and Therapeutic Recommendations in Cases of Uncontrolled Bleeding

A
60
Q

What are the types of Von Willebrand disease?

A

Type 1: Reduced conc of all multmers - most common, Dobie, poodle, GSD, Airdale, Shetland sheepdog

Type 2: Disproporiate loss high MW multimers - German SHP and wirehair = severe bleeding

Type 3: almost complete absence vWF (<.01%) - Shetland sheep dogs, scottish terriers, chesapeake bay retrievers, dutch Kooikers

61
Q

What is Virchow’s triad?

A

1) endothelial injury
2) vascular stasis
3) hypercoagubility

62
Q

What is the pathopysiology of thromboembolism?

A
  1. endothelial damage: decreased ADPase
  2. Platelet agonists: hypoalbulmenima = increased TxA2
  3. Disease states: decreased NO
  4. Drugs: PGi2 inhibition by Cox
  5. Hyperactivty secondary hemostasis:
    - increased exposure TF (damage)
    - neoplasia - TF and procogaulant activates F10
    - AT deficentcy
    - activated protein C deficiency = sepsis, cancer, pancratitis
  6. Hypofibrinolysis - PAI-1 acute phase protein
63
Q

When is a does a low AT increase risk hypercoagubility?

A

<60%

64
Q

What does a PTE look like on rads and what are most common lung lobes?

A

Most common lung lobes = right and caudal

Oligemia: areas of radiolucency on VD or DV (hypovasular lung)

Enlarged main pulmonary a

Attenutatio lobar a or v

Effusion in cats

27% dogs and 0-7% cats have normal rads

65
Q

How do you test for PTE?

A

Supportive:

  • Thoracic rads
  • Arterial blood gas
  • D-dimers - strong neg. predicitve value and supportive if quantive test high (>1000ng/dL)
  • Echocardiography - pulmonary hypertension, thrombus, right MPA and heart enlarged.
  • TEG

Definative:

  • Selective pulmonary angiography - not clincially useful, gold standard
  • non-selective pulmonary andgiography - less sensitve
  • Pulmonary scintigraphy
  • Helical CT pylmonary andiography (CTPA)
66
Q

What are thrombolytic agents?

A

Streptokinase

Urokinase

t-PA (tissue plasminogen activator)

67
Q

What conditions are associatd with feline DIC?

A

40% neoplasia (LSA, carcinoma)

26% pancreatitis

19% sepsis

13% infectious

68
Q

What are causes of DIC?

A

Cytokines = endothelial damage

Leukocyte secreated platelet activiting factor

Decrease AT levels - consumption, impaired hepatic syn, degradation neutrophil elastase

Decreased activated protein C - consumption, cytokine downregulated thrombomodulin on endothelial cell, decrase protein S, impaired hepatic syn

Stimylate PAI-1 = suppress fibrinolysis

69
Q

Underlying condition plus 3 or more of the following factors have been associated with diagnosis of DIC

A

thrombocytopenia

Increased PT, aPTT

Elevated fibrin-split

D-dimers

hypofibrinogenemia

reduced AT activity

red blood cell fragmenation

70
Q

What is refeeding syndrome?

A

Sudden increase insulin = severe hypophosphatemia, hypokalemia and hyperglycemia

71
Q

What is the temperture and timing of a steam sterilizer?

A

emperature and time requirements are interdependent, although typical temperature may be 121° C (250° F) for 30 minutes in a gravity-displacement sterilizer, or 132° C (270° F) for 4 minutes in a prevacuum unit. At higher temperatures, less exposure time is required, and vice versa.

72
Q

Recommended Safe Storage Times for Sterile Packs Using Various Wrapping Materials

A
73
Q

The “anatomy” of an articulating instrument (a needle holder)

A
74
Q

The four blades that fit a #3 scalpel handle (i.e., 10, 11, 12, and 15) and four blades that fit a #4 scalpel handle (i.e., 20, 21, 22, and 23)

A

A Beaver surgical knife handle and selected beaver blades (#64 and #67

75
Q

Three commonly used scissors: A, Curved Mayo; B, curved Metzenbaum; and C, operating (utility) scissors

A

A pair of Westcott scissors

76
Q

Wire-cutting scissors, including A, the “notch” and B, serrated cutting edges

A

Four different rongeurs: two (A, Stille-Luer and B, Ruskin) double-action type and two (C, Lempert and D, Kerrison) single-action type.

77
Q

Four periosteal elevators: A, Freer, B, Sayre, C, ASIF (Synthes/AO), and D, Langenbeck

A

This figure shows each of the following: A, Bone chisel. B, Osteotome. C, Gouge. D, Gigli saw. E, Bone-cutting forceps, and F, a trephine

78
Q

Mayo-Hegar and B, Olsen-Hegar needle holders.

A

Castroviejo needle holder.

79
Q

Right-angle; B, Babcock; C, Allis; and D, Ochsner-Kocher forceps.

A

Noncrushing forceps: A, Doyen intestinal; B, DeBakey; and C, Satinsky forceps

80
Q

Patterns for thoracic and vascular DeBakey (A) and Cooley (B) forceps

A

Three commonly used hemostatic forceps: A, Halsted mosquito; B, Kelly; and C, Crile forceps

81
Q

Brown-Adson; B, DeBakey, C, dressing; and D, Adson forceps

A

Backhaus (penetrating) clamps; and B, Lorna (nonpenetrating) clamps.

82
Q

Figure shows five bone-holding forceps: A, Kern; B, Lane; C, Vebrugge; D, reduction forceps with a speed lock; and E, reduction forceps with points and a ratchet

A

malleable; B, Hohmann retractors; and C, spay (Snook) hooks.

83
Q

Lister bandage scissors; and B, Spencer stitch scissors.

A

Jewelers’ forceps; B, vessel dilators; C, dissecting forceps; and D, tying forceps.

84
Q

Nonlocking microsurgical needle holders with three different types of tips (straight, curved, and extra fine).

A

A microsurgical vessel clamp

85
Q

An Alm microsurgical retractor

A

Comparison of the breaking strength of different tissues across time

86
Q

Composition of collagen in GI submucosa?

A

type 1 = 68%

type 2 = 20%

type 5 = 12%

87
Q
A